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Periodontology 2000, Vol. 67, 2015, 34–57 © 2014 John Wiley & Sons A/S.

ley & Sons A/S. Published by John Wiley & Sons Ltd
Printed in Singapore. All rights reserved PERIODONTOLOGY 2000

Periodontal disease in children


and adolescents of Latin America
J A V I E R E. B O T E R O , C A S S I A N O K U C H E N B E C K E R R OS
€ ING, ANDRES DUQUE,
ADRIANA JARAMILLO & ADOLFO CONTRERAS

Periodontal diseases are a group of inflammatory odontal diseases in children and adolescents of Latin
pathologies that mainly include gingivitis and America, which is the focus of this review, is challeng-
periodontitis. Gingivitis is a prevalent type of peri- ing as problems are encountered in terms of case def-
odontal disease in subjects of all ages, including initions and the availability of adequate scientific
children and adolescents (2, 68, 71). Less prevalent reports. Epidemiological data are scarce for some
periodontal diseases include aggressive periodontitis, parts of Latin America, especially with respect to
acute necrotizing ulcerative gingivitis and diseases of nationwide representative studies (38). The present
herpesvirus and fungal origin (6). Gingivitis and peri- article addresses methodological issues pertaining to
odontitis are considered to be a continuum of the the definition of periodontal disease in children and
same inflammatory process, although it is important adolescents, and then overviews the available epide-
to note that many gingivitis lesions do not progress to miological findings on periodontal diseases of young
periodontitis (46, 89). Immediately after tooth erup- individuals in Latin America and potential risk factors
tion, bacterial biofilm begins to form at tooth surfaces associated with the diseases. Information was
exposed to the oral cavity and in intimate contact retrieved from country-wide studies and from studies
with the gingival margin. The severity of periodontal of selective populations.
disease depends on the level of biofilm accumulation,
the virulence of the biofilm bacteria and the humoral
Search methods
and cellular immune responses to the biofilm micro-
biome. A systematic search was carried out using MEDLINE
Gingivitis in young individuals typically remains (PubMed), LILACS, BIREME and SciELO to obtain
chronic for a prolonged period of time without caus- information on the periodontal condition of children
ing any damage to the periodontal ligament or bone. and adolescents in Latin America. The following
However, an alteration of the balance between the keywords in English, Spanish and Portuguese were
biofilm and the host can give rise to loss of periodon- used in the search: ‘prevalence’, ‘frequency’, ‘gingivi-
tal attachment. Chronic periodontitis and aggressive tis’, ‘prepubertal periodontitis’, ‘juvenile periodonti-
periodontitis start as gingivitis but it has been difficult tis’, ‘aggressive periodontitis’, ‘marginal bone loss’,
to ascertain the biological processes involved in the ‘periodontal disease’, ‘children’, ‘adolescents’ and ‘ul-
progression to periodontitis (7). Microbial dysbiosis, ceronecrotizing gingivitis’. The previous terms used
overgrowth of pathogenic bacteria, herpesvirus reac- for the disease currently known as ‘aggressive peri-
tivation, immune-system disruption and acquired odontitis’ include ‘localized juvenile periodontitis’
and/or genetic susceptibility factors are probably (Fig. 1) and ‘generalized juvenile periodontitis’ (Figs 2
involved in disease progression from gingivitis to and 3), and these older diagnoses were also used in the
periodontitis (23, 31, 70). search of the available literature. The World Health
Epidemiology assesses the prevalence of diseases Organization (98) and the Panamerican Health Orga-
and disease-associated factors in populations. nization databases were also explored and a manual
Epidemiologic data allow the identification of high- search of local journals was performed. In addition,
risk populations and measures of potential value for the internet sites of the Ministry of Health from each
preventing disease. The topic of epidemiology of peri- country were searched for data on oral health issues.

34
Periodontal disease in Latin American children and adolescents

A C

B D

E G

F H
Fig. 1. Radiographic aspect of a
19-year-old patient with localized
aggressive periodontitis. Baseline
radiographs of maxillary (A, C) and
mandibular (E, G) molars show ini-
tial bone levels, and radiographs
taken 1 year later demonstrate rapid
bone-loss progression of the same
maxillary (B, D) and mandibular (F,
H) molars.

Literature reviews of periodontal disease in chil- chronic and aggressive periodontitis. The present
dren and adolescents have previously been published article highlights some of the important issues in peri-
in Periodontology 2000 (2, 43). Therefore, we decided odontal epidemiology.
to focus on information that was not included in ear-
lier publications (i.e. mainly studies published in the
Case definition
past 10 years). The studies included were preferably
of a size sufficient to provide a relatively precise Case definition is one of the most important issues
account of periodontal disease distribution in the in epidemiology, and periodontal disease epidemiol-
various countries of Latin America. ogy is no exception. The definition of gingivitis is rel-
atively simple, but the term ‘aggressive periodontitis’
is surrounded by controversy. One challenging issue
Methodological issues in the case definition of gingivitis (Fig. 4) is the
weight that should be given to gingivitis of little or
Demmer & Papapanou (33) have provided a detailed no clinical significance. If the presence of just one
analysis of methodological issues in the study of site with bleeding on probing in a dentition is the

35
Botero et al.

A B C

Fig. 2. Clinical (A, B, C) and radio-


graphic (D) appearance of general-
ized aggressive periodontitis in
a 16-year-old woman.

cut-off point for the definition of gingivitis, the prev- depth and clinical attachment loss, increases the
alence of gingivitis is practically 100% in all age probability of obtaining an accurate measure of the
groups, including children and adolescents. If assess- periodontal disease status. However, a change in
ing more clinically relevant gingivitis, the high preva- cut-off points and in the number of affected sites
lence figures for gingivitis decrease considerably. It is can result in a very different case definition and
also a matter of debate whether untreated severe prevalence rate of periodontal disease (29, 53, 75).
gingivitis is indeed a necessary prerequisite for Case definition is an important topic in adult peri-
chronic or aggressive periodontitis (previously odontitis, but is not commonly considered in adoles-
known as juvenile periodontitis, prepubertal peri- cents (4) and is rarely considered in children.
odontitis and early-onset periodontitis). A recent Another problem of studying periodontal disease in
review in Periodontology 2000 concludes that young subjects is the lack of periodontal clinical
although unique clinical features may exist for some recordings from dental visits at an early age. Difficult
types of aggressive periodontitis, the clinical differ- child behavior in response to the inherent discom-
ence between aggressive periodontitis and chronic fort of a periodontal examination can complicate
periodontitis is not always discernable (7). Also, the data collection. In addition, assessment of periodon-
microbiology, the inflammatory response and the tal conditions in children can be difficult as a result
outcome of treatment may not differ significantly of the ongoing maturation of the dento–epithelial
between patients with chronic periodontits and junction, a high position of the gingival margin
those with aggressive periodontitis (7, 8, 32, 35, 89). (which may interfere with identification of the ce-
The diagnosis of ulcerative necrotizing periodontal mento–enamel junction and its distance from the
diseases, on the other hand, can be reliably made alveolar bone), altered passive tooth eruption, the
based on distinct clinical signs. presence of a mixed dentition and exfoliation of
The thresholds of clinical parameters used to deciduous teeth.
define the extent and severity of periodontal disease
are also fraught with uncertainty. Probing depths,
Periodontal indices
clinical attachment loss, radiographic bone level and
even tooth loss have been used to define degrees of Periodontal indices have been developed to study the
periodontal disease, but the use of any single clinical epidemiology of periodontal diseases (Table 1). How-
parameter is associated with low diagnostic sensitiv- ever, these indices can differ significantly in their esti-
ity. A combination of parameters, such as probing mation of disease prevalence because of differences

36
Periodontal disease in Latin American children and adolescents

B
Fig. 3. Clinical (A) and radiographic
(B) aspects of a 30-year-old man
with generalized aggressive peri-
odontitis. The patient was otherwise
healthy and presented with advanc-
ed periodontal attachment and bone
loss. Microbial analysis revealed a
subgingival microbiota composed of
Porphyromonas gingivalis (2.2 3 105
colony-forming units/ml), Fusobac-
terium spp. (1.5 3 105 colony-form-
ing units/ml), Prevotella intermedia
(2.9 3 106 colony-forming units/
ml), Tannerella forsythia (9 3 104
colony-forming units/ml), Campylo-
bacter spp. (1.6 3 105 colony-form-
ing units/ml) and Eikenella
corrodens (1.1 3 105 colony-forming
units/ml).

A in case definition and the method of measuring peri-


odontal disease. The use of partial mouth indices can
lead to overestimation or underestimation of disease
prevalence. A recent study of adolescents in Brazil
showed that partial-mouth examination protocols
may underestimate periodontal disease and sug-
gested that examination of at least two diagonal
quadrants may be necessary to quantify periodontal
disease in adolescents and young adults (77). The
Papillary, Marginal, Attached Index was originally
designed for the examination of children, and
although this index includes a score of periodontal
pockets, the severity and extent of more severe dis-
B
ease is not calculated, and the index is highly subjec-
tive. The Periodontal Disease Index was developed by
Ramfjord (81) to measure periodontal disease, but
this index can potentially over- or underestimate dis-
ease severity because only selected teeth are exam-
ined, and clinical attachment loss tends to be
underestimated because of recordings that fall inside
the set ranges of the index. Other periodontal indices
and their diagnostic proficiencies are presented in
Table 1.
The most serious deficiency of periodontal indices
Fig. 4. Mild gingivitis in a 6-year-old male patient (A) and in an is their focus on past periodontal destruction rather
8-year-old female patient (B). Gingival inflammation and pla- than on current or future disease activity. Even
que accumulation are present in the mandibular anterior teeth. gingival bleeding on probing, which is a sign of more

37
Botero et al.

Table 1. Indices used to measure periodontal disease in epidemiological studies

Index Description Extension Considerations


Authors (year)
(reference)
Papillary Marginal P0: normal; no inflammation Partial mouth Extensive, only selected
Attached Gingiva Index teeth are assessed
P1: mild papillary engorgement; slight increase
Schour & Massler Mainly visible
in size
(1950) (57) examination

Schour & Massler P2: obvious increase in size of gingival papilla;


(1947) (100) bleeding on pressure
P3: excessive increase in size of gingival papilla with
spontaneous bleeding
P4: necrotic papilla
P5: atrophy and loss of papilla (through
inflammation)
M0: normal; no inflammation visible
M1: engorgement; slight increase in size;
no bleeding
M2: obvious engorgement; bleeding
on pressure
M3: swollen collar; spontaneous bleeding;
beginning of infiltration into attached gingiva
M4: necrotic gingivitis
M5: recession of the free marginal gingiva below
the cemento–enamel junction as a result of
inflammatory changes
A0: normal, pale rose; stippled
A1: slight engorgement with loss of stippling;
change in color may or may not be present
A2: obvious engorgement of attached gingiva with
marked increase in redness; pocket formation
present
A3: advanced periodontitis; deep pockets evident
Periodontal Index 0: negative. Neither overt inflammation nor loss of Full mouth Composite index, which
Russell (1956) (86) function caused by the destruction of supporting takes into
tissue is noted consideration changes
caused by gingivitis
1: mild gingivitis. Overt inflammation in the free
and periodontitis. The
gingiva is present but does not circumscribe
major disadvantage is
the tooth
that it does not
2: gingivitis. Inflammation surrounds the tooth, consider the degree
but there is no apparent break in the epithelial of periodontal
attachment. destruction (clinical
4: used only when radiographs are available. Early attachment loss)
bone loss is noticeable
6: gingivitis with pocket formation. The epithelial
attachment of gingiva to tooth is broken. There is
no interference with normal function. The tooth
is not loose or drifting
8: advanced destruction with loss of function.
The tooth may be loose or drifting. It may sound
dull on percussion and may be depressible in
the socket

38
Periodontal disease in Latin American children and adolescents

Table 1. (Continued)

Index Description Extension Considerations


Authors (year)
(reference)
Periodontal Disease Index 0: normal gingiva; absence of clinical inflammation Partial mouth Although it measures
Ramfjord (1959) (81) and bleeding clinical attachment
loss, the values
1: slight to moderate gingivitis in some areas around
between the ranges
the tooth
are underestimated.
2: slight to moderate gingivitis around the tooth When index teeth are
3: intense gingivitis; ulceration; bleeding severely affected this
could lead to
4: clinical attachment loss <3 mm overestimation
5: clinical attachment loss 3–6 mm
6: clinical attachment loss >6 mm
Gingival Index 0: normal gingiva; absence of clinical inflammation Full mouth/ Highly subjective.
̈
Loe & Silness (1963) (48) and bleeding partial mouth Does not include
when modified periodontal
1: slight inflammation; absence of bleeding
destruction. Only
2: moderate inflammation; swelling; redness; considers changes
bleeding on probing in the marginal
3: intense inflammation; swelling; morphologic periodontium
changes; spontaneous bleeding
Community Periodontal 0: normal gingival, absence of clinical inflammation Partial mouth It does not consider
Index of Treatment and bleeding periodontal
Needs destruction.
1: bleeding on probing
Ainamo et al. Underestimation and
(1982) (1) 2: bleeding on probing, supra- and subgingival overestimation could
calculus; iatrogenic restorations occur. Not designed
3: shallow periodontal pockets 4–5 mm for children and young
adults (<20 years
4: deep periodontal pockets >6 mm of age)
Extent and Severity Index A tooth site is considered diseased only when loss Partial mouth Frequent
Carlos et al. (1986) (16) of attachment exceeds 1 mm. The result (Extension (28 surfaces) overestimation.
Severity) is expressed as two numbers, in which Descriptive nature
the first is the extension (number of sites) and
the second is the mean clinical attachment loss
(in mm)
Extent and Severity Index Identify the 10 proximal tooth sites that provide Partial mouth
based on partial Extent and Severity estimates of clinical (10 sites)
assessment attachment loss, which are maximally coherent
Papapanou et al. to the full-mouth scores
(1993) (76)

Mean probing depth Six sites per tooth, excluding third molars Full mouth Time consuming.
It provides a more
Mean probing depth = sum of all measurements/
precise assessment
number of teeth 9 6
of the periodontal
condition
Mean clinical Six sites per tooth excluding third molars Full mouth Time consuming.
attachment loss It provides a more
Mean clinical attachment loss = sum of all
precise assessment
measurements/number of teeth 9 6
of the periodontal
condition

serious disease, has not always been included in peri- probing depths, clinical attachment levels and bleed-
odontal indices. The best available periodontal indi- ing-on-probing sites. Radiographic analysis would be
ces employ full-mouth examination with recording of helpful, but may be impractical, or even unethical, in

39
Botero et al.

large epidemiological studies. Contemporary studies regard to treatment needs, the index has been used
only request a radiographic examination if indicated in numerous epidemiological studies. The World
by the clinical information and therefore radiographic Health Organization no longer supports the treat-
epidemiological data are scarce. ment-need part of the index and now also measures
The Community Periodontal Index of Treatment attachment loss instead of periodontal pocket
Needs and the later variant, named the Community depth. The lack of uniformity between the two
Periodontal Index, are perhaps the periodontal indi- World Health Organization indices can complicate
ces most commonly utilized in epidemiological the process of data analysis.
studies (1). These two indices were designed for
population-based studies and are easy to use, but
Language, availability and local
have several disadvantages. For instance, only six
relevance of scientific papers
teeth are examined in children and youngsters
under 20 years of age. This was proposed to avoid Language, availability and local relevance of scientific
mislabeling a deep sulcus, resulting from an erupt- papers are issues in Latin America, where a large pro-
ing tooth, as periodontal disease. Only gingival portion of articles are written in Spanish or Portu-
bleeding and calculus are recorded in young indi- guese and are published in local journals or websites
viduals, which may lead to underestimation of the (i.e. that of the Ministry of Health). Articles not writ-
destructive types of disease. This was illustrated in ten in English may provide important information
the study of Benigeri et al. (10), who found that a but are not readily accessible to researchers outside
tooth with a pocket depth of ≥6 mm was detected the region and hence are not frequently cited. Local
in 8.5% of adults if only two sites were examined studies may also show methodological deficiencies,
per tooth. However, the percentage of teeth with a which must be considered when interpreting the
pocket depth of ≥6 mm increased to 21.4% if prob- published results.
ing was performed in all surfaces of every tooth.
The partial recording system resulted in underesti-
mation of the prevalence of subjects having at least Periodontal disease in Brazil
one tooth with Community Periodontal Index of
Treatment Needs periodontitis scores of 3 and 4. Brazil is the largest country (8,514,877 km2) in Latin
Despite the criticism of the Community Periodontal America, with a population of more than 190 million
Index of Treatment Needs index, especially with and with almost 240,000 dentists (Fig. 5). Brazil is also

Fig. 5. Map showing demographic


information and number of dentists
in Latin American Countries. Dispar-
ity in the number of dentists avail-
able for the population is evident
among the countries (99).

40
Periodontal disease in Latin American children and adolescents

the Latin American country with the greatest number observed an increasing number of periodontal sites
of studies of periodontal disease occurrence of ≥4 mm and a 34% increase in alveolar bone loss
(Table 2). However, large heterogeneity in periodon- (28).
tal case definition and great disparity among popula- Some peculiarities have been published on peri-
tions from various regions of the country make it odontal diseases in children and adolescents from
virtually impossible to merge data from different Brazil. A nationwide epidemiological study of 16,126
studies. adolescents, 15–19 years of age, found that 35.6%
The 2004 nationwide representative survey of 15- had experienced dental and gingival pain in the past
to 19-year-old individuals found, using Community 6 months (14). Significant associations were
Periodontal Index estimates, that 46.2% exhibited observed between dental and gingival pain and
gingival health, 18.8% exhibited gingival bleeding female gender, low income, nonstudents and stu-
and 33.4% exhibited supragingival calculus; regard- dents enrolled in public schools with grades that
less, periodontal pockets of ≥4 mm were present in were low for the age group (14). Also, a higher prev-
fewer than 2% of the study individuals (59). Nicolau alence of oral pain was associated with higher pre-
et al. (66), Antunes et al. (5), Biazevic et al. (11) and valences of dental caries and calculus (14). A study
Freire et al. (36) found gingival bleeding and dental of HIV-infected children, 0–14 years of age, revealed
calculus in approximately 20% of children and ado- that only 12.5% of subjects were plaque-free and
lescents, but virtually no pockets of ≥4 mm. How- that 58.9% showed gingivitis, with an average of 4.4
ever, Maltz & Barbachan e Silva (54), Maltz et al. bleeding sites (84). A study in southern Brazil found
(55), Feldens et al. (34) and Rebelo et al. (82), who a high level of gingivitis in children with cerebral
also used the Community Periodontal Index esti- palsy, which was probably related to poor oral-
mates, demonstrated gingivitis in more than 90% of hygiene habits (40).
Brazilian children and adolescents, and 15–35% A microbiological study of aggressive and chronic
exhibited bleeding gingiva. Nogueira dos Santos periodontitis found that the occurrence of periodon-
et al. (67) found calculus in approximately 50% of topathic bacteria was similar to that reported in other
young subjects. countries (27). Interestingly, the level of periodontitis
A higher prevalence of periodontal breakdown has in adolescents was positively related to the presence
been reported in large studies with full-mouth of leukotoxic Aggregatibacter actinomycetemcomitans
periodontal examination. Cortelli et al. (26), demon- strains (27). A genetic study identified a positive asso-
strated, in the south-east region of Brazil, a prev- ciation between aggressive periodontitis and two
alence of 3.7% for generalized aggressive markers – rs1935881 and rs1342913 – in the FAM5C
periodontitis and a prevalence of 1.7% for localized gene (19).
aggressive periodontitis. Susin & Albandar (92) In sum, the studies from Brazil point to increasingly
found a prevalence of 2.1% for aggressive periodon- severe periodontal disease in subjects with heavy
titis and a prevalence of 18% for chronic periodonti- accumulations of plaque and calculus and of low
tis in 14- to 19-year-old subjects. Susin et al. (91) socio-economic status.
demonstrated gingival recession in almost 30% of
14- to 19-year-old subjects. A radiographic-based
study, performed by Guimaraes et al. (41) in 2- to Periodontal disease in Argentina
11-year-old children, found definite bone loss in
fewer than 1% and questionable bone loss in Argentina is the second-largest country in South
approximately 10% of subjects. A retrospective lon- America and has a population of over 40 million
gitudinal study based on bitewing radiograph exam- (Fig. 5). An epidemiological study of 2,279 children,
ination of 3- to 10-year-old subjects with no obvious 7–8 and 12–13 years of age, was carried out in eight
signs of periodontitis initially found that periodontal different regions of Argentina (30) (Table 3). In the 7–
bone loss increased with age, and the presence of 8 years’ age group, the prevalence of marked gingivi-
tooth surfaces with either caries or restorations tis was 2.7%, compared with the 12–13 years’
increased the probability of bone loss (97). Two age group, in which the prevalence was 27.2%. The
smaller studies of riverside isolated communities author also compared the prevalence of gingivitis
found clinical attachment loss of ≥3 mm in 100% of between two populations of different ethnic origins
the individuals (24) and aggressive periodontitis in and found that native Americans were more affected
approximately 10% (25). One, 52-month longitudinal compared with Caucasians (24.7% versus 15.4%,
study of untreated children and adolescents respectively) (30).

41
Botero et al.

Table 2. Studies of periodontal disease in children and adolescents in Brazil

Authors Number of Male/Female Age Clinical findings Remarks


(year) subjects ratio (years)
(reference)
Maltz & 1,000 students 447/553 12 Full-mouth Gingival Bleeding Representative sample.
Barbachan e from public Index. Prevalence of gingival Gingival Bleeding Index
Silva (2001) and private bleeding in public and private was higher in students
(54) schools schools: 98.1% and 95.7%, from public schools
respectively. Extension of
Gingival Bleeding Index (mean
Gingival Bleeding Index) in
public and private schools: 21.7%
and 14.7%, respectively
Maltz et al. 233 students Not available 8–10 Full-mouth Gingival Bleeding Two school-based
(2001) (55) examined in Index. Mean Gingival Bleeding cross-sectional surveys
1975 and 185 Index in 1975: 24.5%. Mean performed in the
students Gingival Bleeding Index in same school, with
examined in 1996: 35.5% different children,
1996 in 1975 and 1996.
A significant increase
(P = 0.001) was
observed in average
Gingival Bleeding
Index
Cortelli et al. 600 individuals 244/356 15–25 Full-mouth periodontal The presence of
(2002) (26) from the examination and radiographic periodontal destruction
region of Vale examination. Prevalence of was higher in female
do Paraıba localized aggressive periodontitis: students than in male
1.66%. Prevalence of generalized students (P < 0.05)
aggressive periodontitis: 3.66%.
Prevalence of incipient
periodontitis: 14.3%
Nicolau et al. 652 adolescents Not available 13 Full-mouth gingival bleeding 311 families were
(2003) (66) (Community Periodontal Index interviewed and early
score 1). Worst score in each life-course experiences
tooth considered. Prevalence of (such as being born in
gingival bleeding: 99%. Severity a family with a low
of gingival bleeding – individuals socio-economic status,
with <62% of bleeding sites: presently living in an
48.6% overcrowded house,
mother with <8 years
of education, those
with schooling delay,
without nuclear
families and who
experienced severe
paternal punishment)
presented the worst
gingival status
Susin et al. 266 individuals 133/130 14–19 Full-mouth periodontal A high level of gingival
(2004) (91) from a examination. Prevalence of recession was observed
representative gingival recession ≥1 mm: 29.5%. in this population,
sample of the Prevalence of gingival recession mainly related to
metropolitan ≥2 mm: 12.2%. Prevalence of periodontal disease.
area of Porto gingival recession ≥3 mm: 5.9% Analytical model
Alegre demonstrated significant
association with the
presence of calculus
and smoking

42
Periodontal disease in Latin American children and adolescents

Table 2. (Continued)

Authors Number of Male/Female Age Clinical findings Remarks


(year) subjects ratio (years)
(reference)
rio da 7,772
Ministe Not available 15–19 Periodontal examination: Representative sample
 de (2003) individuals
Sau Community Periodontal of the whole country.
(59) from all Index. Prevalence of The worst periodontal
regions in the healthy periodontium: conditions were found in
country 46.18%. Prevalence of less-developed regions
gingival bleeding: 18.77%.
Prevalence of calculus: 33.4%.
Prevalence of 4–5 mm pockets:
1.19%. Prevalence of ≥6 mm
pockets: 0.15%
Susin & 612 individuals 291/321 14–29 Full-mouth periodontal Analytical model
Albandar from a examination. Prevalence of demonstrated significant
(2005) (92) representative aggressive periodontitis in association with
sample of the 14- to 19-year-old-subjects: 2.1% socio-economic status,
metropolitan smoking and the
area of Porto presence of calculus
Alegre
Feldens et al. 490 children 260/230 3–5 Full-mouth visible plaque and Visible plaque and gingival
(2006) (34) from nursery Gingival Bleeding Index. bleeding were positively
schools Prevalence of visible plaque: 99%. associated. Gingival
Prevalence of gingival bleeding: Bleeding Index was more
77% severe in posterior than
in anterior teeth.
Associations were
observed between
gingival bleeding and
gender (boys presented
higher occurrence), low
socio-economic status
and anterior maxillary
teeth without spacing
Nogueira dos 971 individuals 458/513 10–18 Periodontal examination: The study was performed
Santos et al. from public Community Periodontal Index. in two cities, using two
(2007) (67) (municipal Prevalence of healthy sextants different methodologies.
and state) and in municipal, state and private Data from Recife (n = 40)
private schools schools: 31.4%, 244.0% and were not considered.
54.2%, respectively. Prevalence A significant association
of gingival bleeding in municipal, was observed between
state and private schools: 20.4%, the type of school and the
21.6% and 27.0%, respectively. prevalence of periodontal
Prevalence of calculus in conditions, with students
municipal, state and private from private schools
schools: 58.1%, 54.5% and 18.8%, presenting healthier
respectively periodontal states
Costa et al. 44 students 21/23 Mean age Longitudinal study with Despite the reduced
(2007) (28) from a public at 52 months of follow-up. number of individuals, a
school baseline: Periodontal examination: longitudinal approach
12.4 years clinical attachment level and allowed us to understand
bone loss. 34% increase in the progression of
bone loss over time. Prevalence periodontal breakdown
of sites with bone loss in adolescents
increased from 2.1% to 7.5%
(P < 0.001). Increased number
of sites with clinical attachment
loss ≥4 mm

43
Botero et al.

Table 2. (Continued)

Authors Number of Male/Female Age Clinical findings Remarks


(year) subjects ratio (years)
(reference)
Biazevic et al. 247 individuals 130/117 15–17 Periodontal examination: Association between the
(2008) (11) from a Community Periodontal Index. presence of periodontal
cross-sectional Prevalence of healthy sextants: disease approached
population 47.8%. Prevalence of gingival significance with Oral
study bleeding: 39.8%. Prevalence of Health Impact Profile
calculus: 9.7%. Prevalence of (P = 0.053)
pockets 4–5 mm: 2.8%
Corraini et al. 39 individuals 21/18 12–19 Full-mouth periodontal Clinical attachment loss
(2008) (24) from an examination. Prevalence of is highly prevalent.
isolated clinical attachment loss ≥3 mm: Associations were
riverside 100%. Prevalence of clinical observed with smoking
population, attachment loss ≥4 mm: 7.7%. and the presence of
with no access Prevalence of clinical attachment dental calculus
to dental care loss ≥7 mm: 5.1%. Prevalence of
probing depth ≥3 mm: 100%.
Prevalence of probing depth
≥5 mm: 5.1%. Prevalence of
probing depth ≥7 mm: 5.1%
Antunes et al. 1,799 735/1,064 15–19 Periodontal examination: Representative sample.
(2008) (5) adolescents Community Periodontal Index. Gingival bleeding and
from 35 cities Prevalence of healthy sextants: calculus were associated
in the state of 65.7%. Prevalence of gingival with gender (higher values
Sa~o Paulo bleeding: 21.6%. Prevalence were found in male
of calculus: 19.4% subjects), different from
white ethnicity, school
delay and household
crowding. Access to dental
services showed a positive
association with better
periodontal conditions
Rebelo et al. 889 students 399/490 15–19 Full-mouth Lo € e & Silness Gingival Representative
(2009) (82) from public Index. Prevalence of gingival cross-sectional survey
and private bleeding: 53.3%. Reported
schools severity of gingivitis – mild:
78.5%; moderate: 16.1%;
severe: 0.11%.
Corraini et al. 39 individuals 21/18 12–19 Full-mouth periodontal Individuals with aggressive
(2009) (25) from an examination. Prevalence of periodontitis presented
isolated aggressive periodontitis in male high amounts of
riverside subjects: 9.5%. Prevalence of plaque-retaining factors
population, aggressive periodontitis in female
with no access subjects: 11.1%
to dental care
Freire et al. 1,947 students 941/1,006 12 Periodontal examination: Representative sample.
(2010) (36) from public Community Periodontal Index. Students from public
and private Prevalence of healthy schools presented the
schools in periodontium in public and worst periodontal
Goiania private schools: 71.4% and 93.6%, conditions (P < 0.001)
respectively. Prevalence of
gingival bleeding in public and
private schools: 19.1% and 1.3%,
respectively. Prevalence of
calculus in public and private
schools: 9.5% and 5.1%,
respectively

44
Periodontal disease in Latin American children and adolescents

Table 2. (Continued)

Authors Number of Male/Female Age Clinical findings Remarks


(year) subjects ratio (years)
(reference)
Guimaraes 450 healthy 234/216 2–11 Bone loss was measured in Convenience sample from
et al. (2010) children bitewing and periapical dental clinics. Limited
(41) treated in radiographs. Prevalence of external validity.
pediatric definite bone loss of ≥3 mm, No association with
dentistry measured from cemento-enamel age was observed
clinics junction to alveolar bone
crest: 0.85% in male subjects
and 0.46% in female subjects.
Prevalence of questionable
bone loss of >2 mm
but <3 mm, measured
from cemento-enamel
junction to alveolar bone
crest: 9.82% for male subjects
and 6.48% for
female subjects
Bonanato 551 individuals 277/274 5 Gingival bleeding, visible plaque Representative sample.
et al. (2010) from a random and calculus were measured and Analytical approach
(13) sample in Belo a prevalence of 18.5% of indicated an association
Horizonte gingivitis, 45.4% of visible plaque between social and
and 8.9% of calculus was cultural factors and the
observed prevalence of oral
diseases
Susin et al. 619 individuals 291/321 14–19 Full-mouth periodontal Analytical model
(2011) (93) from a examination. Prevalence of demonstrated significant
representative chronic periodontitis in 14- to association with older
sample of the 19-year-old subjects: 18.2% age, socio-economic
metropolitan status and the presence
area of Porto of calculus
Alegre

Chiappe et al. (21) examined the periodontal status odontitis, but Gingival Index scores of, respectively, 1
of 19-year-old individuals enrolled in the School of and 2 were found in 67.7% and 13.4% of the subjects
Dentistry at the University of Buenos Aires. At the (9).
start of the study, 34.7% of periodontal sites exhibited
bleeding on probing and 91% of the students showed
at least one site with bleeding on probing; and 7.9% Periodontal disease in Mexico
of periodontal sites presented ≥1 mm of clinical
attachment loss and 49.6% of the students had at Mexico is the third-largest country in Latin America
least one site with ≥1 mm of attachment loss. In bite- and has the second-largest size of population
wing radiographs, 2.95% of sites presented alveolar (Fig. 5). Five periodontal studies with considerable
bone loss of >2 mm (21). There were no significant population samples (i.e. of more than 300 subjects)
differences between the initial examination and a 2- have been performed in Mexico (Table 4). The first
year follow-up examination in bleeding on probing, study, which included 1,263 children of 13–17 years
clinical attachment loss and alveolar bone loss (21). of age, found a prevalence of gingivitis of 44%
Moreno & Esper (63) studied incisors and first molars using the Russel Index (PI) (73). The next three
in subjects 14–18 years of age and found prevalences studies examined a sample of 300–500 children of
of 1 and 2 mm of clinical attachment loss to be 39.8% 4–16 years of age and found a prevalence of gingi-
and 7.4%, respectively (63). Barletta et al. (9) exam- vitis of 13–70% (45, 64, 74). The most representa-
ined 14- to 15-year-old subjects from two schools in tive study included 25,764 young individuals (88).
La Plata, Argentina. They detected no signs of peri- This study demonstrated that the 6- to 9-year’ age

45
Botero et al.

Table 3. Studies of periodontal disease in children and adolescents in Argentina

Authors Number of Male/Female Age Clinical findings Remarks


(year) subjects (% or number) (years)
(reference)
de Mun~ iz 2,279 Not available 7–8 75% presented with plaque Oral Health survey.
(1985) (30) 12–13 deposits. Prevalence of Calculus and gingivitis
calculus was 0.4% in increased with age.
7-year-old subjects and A lack of adequate dental
16.1% in 13-year-old care was found in all
subjects. Prevalence of regions evaluated
gingivitis was 2.7% in
7-year-old subjects and
27.2% in 13-year-old subjects
Chiappe et al. 475 dental 31.7%/68.3% 19 Prevalence of gingivitis was After studying dentistry
(1997) (21) students. Two 91%, measured as bleeding for 2 years the
years later 240 on probing positive in at prevalence of gingivitis
dental students least one site. Prevalence was similar but the
were of alveolar bone loss >2 mm severity was lower.
re-examined was 3.0% and in no subjects Periodontal condition
did measurements exceed was not substantially
3 mm modified
Moreno & 394 227/167 14–18 Clinical attachment loss Minimal clinical
Esper (2003) of 1 mm= 38.9% and of attachment loss was
(63) 2 mm=7.4% observed and in no
case exceeded 2 mm
Barletta et al. 149 57.6%/42.4% 14–15 67.7% with Gingival Index Gingival Index was used.
(2006) (9) score = 1 No signs of periodontitis
13.4% with Gingival Index were observed. None of
score = 2 the subjects presented a
Gingival Index score of 3.
However, 32.8% of
subjects had gingival
bleeding

group was almost free of gingival inflammation ing age. Unfortunately, no studies have attempted
(Community Periodontal Index score 0 = 91.7%); to quantify the level of aggressive periodontitis in
the 10- to 14-year’ age group still presented high Mexico.
figures of health (Community Periodontal Index
score 0 = 83.3%), despite the fact that 10.3% pre-
sented with gingivitis and 6.4% with calculus; and Periodontal disease in Colombia
the 15- to 19-year’ age group revealed periodontal and Venezuela
health in only half of the subjects, with 18.7% pre-
senting with gingivitis, 15.9% with calculus, and, Colombia is the fifth country in size in Latin America
although 1.2% had pockets of 4–5 mm, only 0.2% with a population of over 40 million (Fig. 5). In 1998,
showed pockets of >6 mm (88). Two studies Colombia conducted the third National Study of Oral
assessed gingival inflammation in a sample of <80 Health in rural and urban regions (83) (Table 5). Gin-
subjects with ages between 4–5 and 10–19 years gival bleeding on probing was observed in 72.1% of 7-
and found prevalences of gingivitis of 39% and year-old subjects and in 84.1% of 12-year-old subjects
71.6%, respectively (18, 94). Another study exam- (83). Calculus and defective dental fillings were found
ined bitewing radiographs of 4-year-old children in 60.9% of the 7- to 12-year-old subjects (83). In the
and found a frequency of marginal bone loss of group of 15- to 19-year-old subjects, 89.2% presented
7.8% (17). A common finding in the studies from with gingival bleeding and 60.9% presented with cal-
Mexico was that poor plaque control and low culus and defective dental fillings (83). All gingivitis
socio-economic status increased the frequency of patients required periodontal treatment according to
gingivitis, and gingivitis also increased with increas- the Community Periodontal Index of Treatment

46
Periodontal disease in Latin American children and adolescents

xico
Table 4. Studies of periodontal disease in children and adolescents in Me

Authors Number Male/Female Age Clinical findings Remarks


(year) of (% or (years)
(reference) subjects number)

Carranza 115 Not 4 7.8% presented marginal bone loss Bitewing radiographs were
et al. (1998) available used to assess marginal
(17) bone loss. Incipient
marginal bone loss was
observed at an early age
Carrillo et al. 74 44.6%/ 10–19 Gingivitis 71.6% Ramfjord Periodontal Disease
(2000) (18) 55.4% Index was used to assess
periodontal tissues.
Gingival inflammation
showed a tendency to
increase with age,
Ramfjord Index scores
of 2 and 3 were obtained
Orozco et al. 1,263 45.1%/ 13–17 Gingivitis 44% Ramfjord’s Periodontal
(2002) (73) 54.9% Disease Index was used to
assess periodontal tissues.
Economic status influenced
the prevalence of the disease:
low-income populations
had a higher prevalence
of gingivitis
Murrieta 389 Not 8–12 Gingivitis 20.6% Gingival Index was used to
et al. (2004) available assess inflammation.
(64) Gingival inflammation
lower than expected. Poor
oral hygiene was the main
indicator for gingivitis
rez-Lo
Jua  pez 382 48%/52% 4–6 Gingivitis 70% (PI) Gingival inflammation was
et al. (2005) highly prevalent and
(45) increased with age

Ortega et al. 590 45.3%/ 13–16 Gingivitis 13.7% No periodontal probe was
(2007) (74) 54.7% <13 years old: 12.3% gingivitis used; a visual
>14 years old: 60.5% gingivitis examination was performed.
The prevalence of gingivitis
increased with age
SIVEPAB 25,764 Not 6–9 Community Periodontal Index score 0 = 91.7% Large scale National Oral
(2010) (88) available health survey with a
Community Periodontal Index score 1 = 7.1%
representative sample.
Community Periodontal Index score 2 = 1.2% Periodontal pockets of
10–14 Community Periodontal Index score 0 = 83.3% 4–5 mm appeared in the
15- to 19-year-old
Community Periodontal Index score 1 = 10.3% subjects and the presence
Community Periodontal Index score 2 = 6.4% of pockets
of >6 mm was very low
15–19 Community Periodontal Index score 0 = 64.1%
Community Periodontal Index score 1 = 18.7%
Community Periodontal Index score 2 = 15.9%
Community Periodontal Index score 3 = 1.1%
Community Periodontal Index score 4 = 0.2%

47
Botero et al.

Table 4. (Continued)

Authors Number Male/Female Age Clinical findings Remarks


(year) of (% or (years)
(reference) subjects number)

Taboada & 77 51.9%/ 4–5 Gingival inflammation 39% Papillary Marginal


Talavera 48.1% Attached Gingival Index
(2011) (94) was used. Gingivitis starts
at an early age and was
associated with poor
plaque control. O’Leary
plaque index was 75.4%
PDI, periodontal disease index.

Needs (83). Deep periodontal pockets, as defined by tions such as acute herpetic gingivostomatitis, mea-
the Community Periodontal Index of Treatment sles and leukemia. Low socio-economic status,
Needs, were observed in 1% of the 7- to 12-year-old malnutrition and poor oral hygiene habits were
individuals (83). Of the 15- to 19-year-old subjects, identified as contributory factors. Microbiological
31.4% exhibited localized attachment loss and 1.4% examination of noma lesions identified gram-nega-
generalized attachment loss (83). Clinical attachment tive bacteria, Neisseria species, fusiform bacilli, Lepto-
loss in 15- to 19-year-old subjects was slight (1– trichia buccalis and fungi.
2.9 mm) in 31%, moderate (3–4 mm) in 1.7% and Periodontal data from Venezuela are scarce. Navaz
severe (>5 mm) in 0.1%, according to the Extent and et al. (65) found a prevalence of gingivitis of 40–60%
Severity Index (76). No attachment loss was seen in in children 6–9 years of age, and this high prevalence
67.3% of the study subjects. was associated with unfavorable attitudes and low
Go mez-Restrepo et al. (39), in a large random sam- educational level of the parents. Another study (12)
ple of 14- to 17-year-old individuals, found clinical found that necrotizing ulcerative gingivitis was more
attachment loss of ≥1 mm in 40.6% of subjects, of prevalent (32,44%) in the 15–20 age group than adults
≥2 mm in 29.9% and of ≥3 mm in 16.0%, and attach- and it was associated with previous history of gingivi-
ment loss was greater in male subjects than in female tis and poor oral hygiene.
subjects (P < 0.05). Interproximal attachment loss of
≥1 mm, ≥2 mm and ≥3 mm was, respectively, 34.2%,
21.4% and 11.7% (39). Orozco et al. (72) found that in Periodontal disease in Chile
7- to 14-year-old subjects from a native island com-
munity, 45.4% had a Community Periodontal Index Large population studies have been conducted in
of Treatment Needs score of 1, 40.9% had a score of 2 Chile (Table 6). In 1991, Lo pez et al. (50) reported a
and 13.7% had a score of 3. In the 15- to 19-year old prevalence of aggressive periodontitis of 0.32% in
subjects, a Community Periodontal Index of Treat- 2500 adolescents, 15–19 years of age. Another large
ment Needs score of ≥2 was observed in 77.8% of study of 9,163 individuals, of 12–21 years of age,
subjects and a Community Periodontal Index of found that clinical attachment loss of ≥1 mm
Treatment Needs score of 4 was found in 11.1% (72). occurred in 69.2% of the study subjects, of ≥2 mm in
These results point to increased severity of periodon- 16.0% and of ≥3 mm occurred in 4.5% (51). Interprox-
tal disease in communities with low access to imal clinical attachment loss of ≥1 mm was observed
professional dental care. However, in another native in 56.4% of the study subjects, of ≥2 mm in 13.1% and
community from the southeast of Colombia, Triana of ≥3 mm in 3.7% (51). The mean number of peri-
et al. (95) found a lower need for treatment (Commu- odontal sites with clinical attachment loss of ≥1 mm
nity Periodontal Index of Treatment Needs score ranged from 4.3 to 6.6, with clinical attachment loss
0 = 59.7%, score 1 = 30.5% and score 2 = 9.7%) in of ≥2 mm in 2.6–4.3 sites and of ≥3 mm in 1.5–4.0
children 7–12 years of age. sites (51). Clinical attachment loss was positively
Between 1965 and 2000, Jime nez et al. (44) associated with infrequent tooth brushing, dental vis-
described children and adolescents with acute necro- its <1 year ago and attending a government-sup-
tizing ulcerative gingivitis (n = 29), necrotizing ulcer- ported school. A national study of oral health in 2007
ative periodontitis (n = 7) and noma/cancrum oris found that the frequency of gingivitis increased with
(n = 9). The individuals were not infected with HIV, age, as follows: 2-year-old subjects, 2.6%; 4-year-old
but virtually all presented with predisposing condi- subjects, 6.2%; 6-year-old subjects, 55%; and 12-year-

48
Periodontal disease in Latin American children and adolescents

Table 5. Studies of periodontal disease in children and adolescents in Colombia and Venezuela

Country Authors Number of Male/ Age Clinical findings Remarks


(year) subjects Female (years)
(reference) (% or
number)

Colombia Ministerio de 2,682 Not 7–19 Extent and Severity Large-scale oral health
Salud (1999) available Index 21%: 1.1 mm. survey. Gingivitis was
(83) Gingivitis 72.1% in highly prevalent.
7-year-old subjects; Community Periodontal
gingivitis 84.1% in Index of Treatment Needs
12-year-old subjects. and Extent and Severity
Periodontal pockets Index. Periodontal pockets
of >5 mm in 15- to were only
19-year-old observed with increasing
subjects: 1% age
Colombia Orozco et al. 40 Not 7–19 65% of subjects with More than half of the
(2004) (72) available Community sample required some
Periodontal Index type of periodontal
of Treatment Needs treatment
score of > 1, and
complex periodontal
treatment needs in
11.1% of those
subjects
Colombia Triana et al. 82 Not 7–12 30.5% with Community Better oral health
(2005) (95) available Periodontal Index of conditions in this
Treatment Needs population compared
score of 1 and 9.7% with Oral Health National
with Community Survey data
Periodontal Index
of Treatment Needs
score of 2
Colombia Jimenez et al. 45 Not 2–26 Necrotizing ulcerative Not a population-based
(2005) (44) available gingivitis: 29 subjects study. Reflects socio-
(64.4%). Necrotizing economic and hygiene
ulcerative periodontitis: conditions associated
7 (15.6%). Noma: 9 (20%) with necrotizing
periodontal diseases such
as necrotizing ulcerative
gingivitis and necrotizing
ulcerative periodontitis.
Patients with no HIV
infection, in contrast with
other reports
Colombia Go mez- 629 49.8%/ 14–17 The prevalence of clinical Students randomly
Restrepo 50.2% attachment loss selected from public
et al. (2008) ≥1 mm was 40.6%; schools of low and
(39) of ≥2 mm was 29.9%; medium socio-economic
and of ≥3 mm levels. Male gender was
was 16% associated with a higher
probability of having
clinical attachment loss,
using a logistic regression
model
Venezuela Navaz et al. 132 Not 6–9 40–60% presented Gingivitis was frequently
(2002) (65) available with a gingival index associated with the
of 1 unfavorable attitudes
and low educational level
of the parents

49
Botero et al.

Table 6. Studies of periodontal disease in children and adolescents in Chile

Authors (year) Number of Male/Female Age Clinical findings Remarks


(reference) subjects (% or (years)
number)

 pez (1991) (50)


Lo 2,500 52.7%/47.3% 15–19 Aggressive periodontitis After initial screening,
0.32% 27 subjects were
suspected as having
aggressive periodontitis.
Only in eight was
this confirmed by
clinical and radiographic
examinations
 pez et al.
Lo 9,163 4,652/4,510 12–21 Overall clinical attachment Overall, clinical attachment
(2001) (51) loss of ≥1 mm was loss was highly frequent in
observed in 69.2% of the adolescents. Nonetheless,
students, clinical attachment more extensive clinical
loss of ≥2 mm was observed attachment loss of ≥4 mm
in 16% and clinical was less frequent (<2% of
attachment loss of ≥3 mm subjects). Variables such as
was observed in 4.5%. infrequent toothbrushing,
Interproximal clinical dental visits more than
attachment loss of ≥1 mm 1 year ago and attending a
was observed in 56.4% of school that receives
the students, interproximal government support showed
clinical attachment loss of a positive association with
≥2 mm was observed in clinical attachment loss
13.1% and interproximal
clinical attachment loss of
≥3 mm was observed in
3.7%.
Mean number of sites with
clinical attachment loss of
≥1 mm = 4.3–6.6; with
clinical attachment loss of
≥2 mm = 2.6–4.3; and with
clinical attachment loss of
≥3 mm = 1.5–4.0
 pez et al.
Lo 9,163 4,653/4,510 12–21 Necrotizing ulcerative Diabetes and lack of dental
(2002) (52) gingivitis 6.7% check-ups were associated
with necrotizing ulcerative
gingivitis
MINSAL 500 Not available 2 Gingivitis 2.6% National Health survey.
(2007) (62) Gingival inflammation
increases with age and is
more prevalent in the
low-income population
506 Not available 4 Gingivitis 6.2% National Health survey.
Gingival inflammation
increases with age and is
more prevalent in the
low-income population
6 Gingivitis 55% Number of subjects not
reported, which makes
analysis difficult
Soto et al. 2,232 1,093/1,139 12 Healthy 33%; gingivitis 67% The prevalence of gingivitis
(2007) (90) was higher in rural areas.
Calculus prevalence was
28.1%

50
Periodontal disease in Latin American children and adolescents

Table 6. (Continued)

Authors (year) Number of Male/Female Age Clinical findings Remarks


(reference) subjects (% or (years)
number)

Varas et al. 1,637 Not available 6–8 Gingivitis 29.57%; 2.08% Community Periodontal Index
(2008) (96) presented calculus of Treatment Needs index
was used. Gingival bleeding
increased with age

old subjects, 66% (20, 62, 90). Varas et al. (96) found 4.0% of the subjects (22). Interproximal attachment
 pez
gingivitis in 29.6% of 6- to 8-year-old children. Lo loss of ≥1 mm occurred in 33.6%, of ≥2 mm in 10.9%
et al. (52) studied 9,163 subjects, 12–21 years of age, and of ≥3 mm in 3.5% of the subjects (22).
and detected acute necrotizing ulcerative gingivitis in
6.7% (52). They identified an association between
acute necrotizing ulcerative gingivitis and diabetes Periodontal disease in Bolivia,
and lack of periodic dental visits (52). Rivera et al. Ecuador, Paraguay and Uruguay
(85), in a study of rural children of 4–5 years of age,
found gingivitis (9.2%) and caries (49.2%) to be asso- In 1995, The Panamerican Health Organization and
ciated with poor oral hygiene (85), but the prevalence the World Health Organization examined the oral
of gingivitis was lower than previously reported health situation in Bolivia (69). In children 6–15 years
(20, 62). of age, 39% revealed slight gingival inflammation
and 34% moderate gingival inflammation. Only 27%
were essentially free of gingival inflammation (69)
Periodontal disease in Nicaragua, (Table 8). The National Study in Oral Health in Ecua-
Panama, Cuba and the Dominican dor (60) reported a prevalence range of 30–44% for
Republic gingivitis in children 6–12 years of age. Gingivitis was
more prevalent (44%) in the 10–11 years’ age group
The most northern region of Latin America encom- and lower in the 12 years’ age group (30%), which
passes several small countries and some Caribbean may indicate a tendency for reduced periodontal dis-
nations (Fig. 5). National surveys on periodontal dis- ease with increasing age in early puberty (60)
ease in Central America are scarce (Table 7). Medina (Table 8). The National Survey of Oral Health in Para-
et al. (58) studied 1,080 children, 5, 12 and 15 years of guay found that 54.5% of 12- to 15-year-old subjects
age, from urban and rural locations in Nicaragua. were periodontally healthy, 38.8% showed slight
They found gingivitis in 77% of the 12-year-old sub- gingivitis and 6.7% revealed both gingivitis and calcu-
jects and in 68.5% of the 15-year-old subjects (58), and lus (61) (Table 8). A study from Uruguay (15) found
gingivitis was more prevalent (> 90% in same age one patient (1%) with localized aggressive periodonti-
groups) in the rural population (58). Periodontal pock- tis in a small sample of 11- to 18-year-old subjects.
ets of >5 mm were not found in children, but were a Another study (3) in Uruguay in 76 HIV infected
common finding in adults over 30 years of age. children found a prevalence of 75% for gingivitis and
The national study of oral health in Panama (37) 0.7% for necrotizing ulcerative gingivitis.
̈
included 3,763 children of 6–19 years of age. The Loe
and Silness Gingival Index revealed that slight gingival
inflammation (Gingival Index = 0.63–0.73) was pres- Concluding remarks and future
ent in 55.0% of the young population. Three studies perspectives
from Cuba (78–80), of 2- to 12-year-old children,
found a prevalence of gingivitis of 20–52% and a rela- This review shows that inflammatory periodontal dis-
tionship between gingivitis and poor nutritional con- eases are prevalent in children and adolescents in
dition. In the Dominican Republic, Collins et al. (22) Latin America. Gingivitis affects 34.7% of young Latin
examined the periodontal status of 12- to 21-year-old American individuals (Fig. 6), with the highest preva-
subjects. Gingivitis was detected in 39% of the sub- lences found in Colombia (77%) and Bolivia (73%)
jects (22). Clinical attachment loss of ≥1 mm was and the lowest prevalence in Mexico (23%). The
present in 49.5%, of ≥2 mm in 15.0% and of ≥3 mm in prevalence of gingivitis ranged from 31 to 56% in the

51
Botero et al.

Table 7. Studies of periodontal disease in children and adolescents in Nicaragua, Panama, Cuba and the Dominican
Republic

Country Authors Number of Male/Female Age Clinical Remarks


(year) subjects (% or number (years) findings
(reference)

Nicaragua Medina et al. 1,080 50%/50% 5–15 Urban The Community


(2007) (58) Periodontal Index of
12 years of age: 77%
Treatment Needs
gingivitis
index was used.
15 years of age: 68.5% Rural areas
gingivitis presented more
>5 mm pockets 0% periodontal disease
and were associated
Rural with household
12 years of age: 96.5% income. The
gingivitis presence of
gingivitis and depth
15 years of age: 97.5% of periodontal
gingivitis pockets increased
>5 mm pockets 0% with age


Panama Galvez et al. Total number of Not available 6–11 Gingivitis 55.9%. National oral health
(2008) (37) subjects = 10,063: 12 Gingival Index: 0.66 survey with a
Lo pez et al. 3,763 were children 13–18 in 6- to 11-year-old representative
(2010) (49) and adolescents 19 subjects; 0.72 in sample. Gingival
12-year-old subjects; Index was used.
0.71 in 13- to 18-year- Slight gingival
old subjects; and 0.73 inflammation was
in 19-year-old subjects prevalent and
increased with age
Cuba Quin~ onez 230 Not available 2–5 Gingivitis 20% Gingivitis was
et al. (2004) associated with
(78) poor nutritional
condition
Cuba Quin~ onez 52 Not available 5–12 Gingivitis 52% Gingivitis was
et al. (2006) associated with poor
(79) nutritional condition
Cuba Quin~ onez 400 Not available 2–5 Gingivitis 52% Gingivitis was
et al. (2008) associated with poor
(80) nutritional condition
Dominican Collins et al. 1,963 952/1,021 12–21 Overall, 49.5% of the Oral health survey.
Republic (2005) (22) students examined had Logistic regression
at least one site with model revealed that
clinical attachment loss only age significantly
of ≥1 mm; clinical increased the
attachment loss was probability of having
≥2 mm in 15% and clinical attachment
≥3 mm in 4.0% of the loss
students. 33.6% of
students had
interproximal clinical
attachment loss of
≥1 mm; 10.9% had
interproximal clinical
attachment loss of
≥2 mm and 3.5% had
interproximal clinical
attachment loss of
≥3 mm

52
Periodontal disease in Latin American children and adolescents

Table 8. Studies of periodontal disease in children and adolescents in Bolivia, Ecuador, Paraguay and Uruguay

Country Authors (year) Number of Male/Female Age Clinical findings Remarks


(reference) subjects (% or (years)
number)

Bolivia Ocampo & Baez 2,410 Not available 6–15 Community Representative sample. The
(1997) (69) Periodontal Index Community Periodontal
score 0 = 27% Index was used and
increased with age in all
Community
locations. Gingivitis and,
Periodontal Index
in general, poor oral health
score 1 = 39%
was associated with lack of
Community preventive programs
Periodontal Index
score 2 = 34%
Ecuador Ministerio de 2,757 Not available 6–7 Gingivitis 39% Information regarding
Salud Publica pockets was not considered
8–9 Gingivitis 42%
(1988) (60) because the periodontal
10–11 Gingivitis 44% examination process was
12 Gingivitis 30% not explained in the article

Paraguay Ministerio de 1,442 Not available 12–15 Community National Oral health survey.
Salud (2008) Periodontal Index Gingivitis was highly
(61) score 0 = 54.5% prevalent
Community
Periodontal Index
score 1 = 38.8%
Community
Periodontal Index
score 2 = 6.7
Uruguay Campi et al. 100 Not available 11–18 Aggressive After initial screening, just one
(1996) (15) periodontitis 1% case was compatible with
the characteristics of juvenile
periodontitis

remaining countries. Gingivitis needs to be identified


and treated in young individuals as it poses a risk for
development of periodontitis when such individuals
become adults (47, 87). The average rate of periodon-
titis in the young population in Latin America was
<10%. However, the number of studies on periodontitis
in children and adolescents is very limited and addi-
tional studies are warranted. The most common risk
factors for periodontal disease in Latin America
are poor oral hygiene and low socio-economic
Fig. 6. Adjusted prevalence estimate of gingivitis in Latin status.
America. The adjusted prevalence was calculated by Nonetheless, despite the need for more studies, the
including the total number of subjects and the number of
information currently available is very useful for
subjects with gingivitis from at least one representative
study in each country. The dotted vertical line indicates establishing national policies on the promotion, pre-
the adjusted prevalence of gingivitis in Latin American vention and treatment of periodontal disease.
countries (34.7%; 95% CI, 34.4–35.1). The box given for Destructive periodontal disease can be expected to be
each country represents the mean prevalence and is rela- reduced or avoided if prevention and treatment of
tive in size according to the number of subjects included.
severe gingivitis is initiated early in life. The possibil-
Horizontal bars and ticks represent the minimum and
maximum prevalence reported in the studies included. ity that untreated periodontal disease can negatively
Boxes without horizontal bars are the results from only affect the general health puts extra pressure on
one national health study from a specific country. improving the periodontal health of young people in

53
Botero et al.

Latin America. Effective allocation of health-care 10. Benigeri M, Brodeur JM, Payette M, Charbonneau A,
resources depends on the identification of high-risk Isma€ıl AI. Community periodontal index of treatment
needs and prevalence of periodontal conditions. J Clin Pe-
populations and the institution of efficient and low-
riodontol 2000: 27: 308–312.
cost therapies. Figure 5 shows a great disparity in the 11. Biazevic MG, Rissotto RR, Michel-Crosato E, Mendes LA,
dentist/population ratio among Latin American Mendes MO. Relationship between oral health and its
countries (56). Limited access to dental care, espe- impact on quality of life among adolescents. Braz Oral Res
cially in rural and low socio-economic status commu- 2008: 22: 36–42.
12. Blanco BL, Caldero  n A. Comportamiento de la gingivitis
nities, may explain, in part, the relatively high
ulceronecrotizante aguda. Departamento de estomato-
prevalence of periodontal disease among young peo- logıa de Conuco Viejo. Rev Med Electro n 2010: 32. URL:
ple in Latin America. http://www.revmatanzas.sld.cu/revista%20medica/ano%
The use of oral home-care products (toothpaste 202010/vol3%202010/tema4.htm [Accessed 12 October
and toothbrushes) has increased, but seems to have 2011].
had little effect on the prevalence of gingivitis. Data 13. Bonanato K, Pordeus IA, Moura-Leite FR, Ramos-Jorge
ML, Vale MP, Paiva SM. Oral disease and social class in a
from Brazil indicated a per-capita increase, between
random sample of five-year-old preschool children in a
1992 and 2002, of 38% in toothpaste, 138% in tooth- Brazilian city. Oral Health Prev Dent 2010: 8: 125–132.
brushes and 177% in dental floss, and the use of oral 14. Borges CM, Cascaes AM, Fischer TK, Boing AF, Peres MA,
health-care products has further increased from 2002 Peres KG. Dental and gingival pain and associated factors
to 2006 (42). Those data show that there is a general among Brazilian adolescents: an analysis of the Brazilian
Oral Health Survey 2002-2003. Cad Saude Publica 2008: 24:
concern for good oral health, but effective strategies
1825–1834.
for delivering efficient, safe and low-cost preventive 15. Campi M, Esquenasi J, Mercedes A. Prevalencia de la peri-
care have still to be identified and implemented in odontitis juvenil en un grupo de jo venes en la ciudad de
Latin America. Canelones. Odontol Urug 1996: 45: 5–11.
16. Carlos JP, Wolfe MD, Kingman A. The extent and severity
index: a simple method for use in epidemiologic studies of
References periodontal disease. J Clin Periodontol 1986: 13: 500–505.
17. Carranza F, Garcia-Godoy F, Bimstein E. Prevalence of
1. Ainamo J, Barmes D, Beagrie G, Cutress T, Martin J, marginal alveolar bone loss in children. J Clin Pediatr Dent
Sardo-Infirri J. Development of the World Health Organi- 1998: 23: 51–53.
zation (WHO) community periodontal index of treatment 18. Carrillo J, Castillo M, Herna ndez HG, Zermen ~ o J. Estudio
needs (CPITN). Int Dent J 1982: 32: 281–291. epidemiolo gico de las enfermedades periodontales en pa-
2. Albandar JM, Tinoco EM. Global epidemiology of peri- cientes que acuden a la facultad de estomatologıa de la
odontal diseases in children and young persons. Periodon- UASLP. Rev ADM 2000: 57: 205–213.
tol 2000 2002: 29: 153–176. 19. Carvalho FM, Tinoco EM, Deeley K, Duarte PM, Faveri M,
3. Alvarez L, Hermida L, Cuitin ~ o E. Situacio
 n de salud oral Marques MR, Mendoncßa AC, Wang X, Cuenco K, Menezes
de los nin~ os uruguayos portadores del virus de la inmu- R, Garlet GP, Vieira AR. FAM5C contributes to aggressive
nodeficiencia humana. Arch Pediatr Urug 2007: 78: 23– periodontitis. PLoS ONE 2010: 5: e10053.
28. 20. Ceballos M, Acevedo C, Cordova J, Corsini G, Jans A, Bus-
4. American Academy of Periodontology. Research, Science tos L, Del Valle C. Diagno  stico en salud bucal de nin~ os de
and Therapy Committee. Periodontal diseases of children 2 y 4 an ~ os que asisten a la educacio n preescolar. Regio n
and adolescents. Pediatr Dent 2008–2009: 30(Suppl. 7): Metropolitana 2007. Rev Soc Chil Odontopediatrıa 2008:
240–247. 23: 19.
5. Antunes JL, Peres MA, Frias AC, Crosato EM, Biazevic MG. 21. Chiappe V, Go  mez M, Pedreira P, Galeano A, Grinfeld A,
Gingival health of adolescents and the utilization of dental Viale J, Sznajder N. Longitudinal study of periodontal con-
services, state of Sa~o Paulo, Brazil. Rev Saude Publica dition in students of the Dental School the University of
2008: 42: 191–199. Buenos Aires Argentina. Acta Odontol Latinoam 1997: 10:
6. Armitage GC. Development of a classification system for 117–132.
periodontal diseases and conditions. Ann Periodontol 22. Collins J, Carpio AM, Bobadilla M, Reyes R, Gu  zman I,
1999: 4: 1–6. Martınez B, Gamonal J. Prevalence of clinical attachment
7. Armitage GC, Cullinan MP. Comparison of the clinical fea- loss in adolescents in Santo Domingo, Dominican Repub-
tures of chronic and aggressive periodontitis. Periodontol lic. J Periodontol 2005: 76: 1450–1454.
2000 2010: 53: 12–27. 23. Contreras A, Slots J. Mammalian viruses in human peri-
8. Armitage GC. Comparison of the microbiological features odontitis. Oral Microbiol Immunol 1996: 11: 381–386.
of chronic and aggressive periodontitis. Periodontol 2000 24. Corraini P, Baelum V, Pannuti CM, Pustiglioni AN, Romito
2010: 53: 70–88. GA, Pustiglioni FE. Periodontal attachment loss in an
9. Barletta L, Klein PL, Garcıa-Frontini ME, Tau DG, Friso E, untreated isolated population of Brazil. J Periodontol 2008:
Di Salvi N, Soto RR, Urrutia MI. Observations of the peri- 79: 610–620.
odontal status of an adolescent’s population. Rev Fundac 25. Corraini P, Pannuti CM, Pustiglioni AN, Romito GA, Pusti-
Juan Jose Carraro 2006: 11: 20–23. glioni FE. Risk indicators for aggressive periodontitis in an

54
Periodontal disease in Latin American children and adolescents

untreated isolated young population from Brazil. Braz 42. Jardim JJ, Alves LS, Maltz M. The history and global market
Oral Res 2009: 23: 209–215. of oral home-care products. Braz Oral Res 2009: 23(Suppl.
26. Cortelli JR, Cortelli SC, Pallos D, Jorge AO. Prevalence of 1): 17–22.
aggressive periodontitis in adolescents and young adults 43. Jenkins WMM, Papapanou PM. Epidemiology of periodon-
from Vale do Paraıba. Pesqui Odontol Bras 2002: 16: 163– tal disease in children and adolescents. Periodontol 2000
168. 2001: 26: 16–32.
27. Cortelli JR, Cortelli SC, Jordan S, Haraszthy VI, Zambon JJ. 44. Jimenez M, Duke FL, Baer PN, Jones SB. Necrotizing ulcer-
Prevalence of periodontal pathogens in Brazilians with ative periodontal diseases in children and young adults in
aggressive or chronic periodontitis. J Clin Periodontol Medellin, Colombia, 1965-2000. J Int Acad Periodontol
2005: 32: 860–866. 2005: 7: 55–63.
28. Costa FO, Cota LO, Costa JE, Pordeus IA. Periodontal dis- 45. Juarez-Lo pez MLA, Murrieta-Pruneda JF, Teodosio-Proco-
ease progression among young subjects with no preven- pio E. Prevalencia y factores de riesgo asociados a en-
tive dental care: a 52-month follow-up study. J Periodontol fermedad periodontal en preescolares de la Ciudad de
2007: 78: 198–203. Me xico. Gac Med Mex 2005: 141: 185–189.
29. Costa FO, Guimaraes AN, Cota LO, Pataro AL, Segundo 46. Kinane DF, Attstrom R. Advances in the pathogenesis of
TK, Cortelli SC, Costa JE. Impact of different periodontitis periodontitis consensusreport of the fifth European work-
case definitions on periodontal research. J Oral Sci 2009: shop in periodontology. J Clin Periodontol 2005: 32(Suppl.
51: 199–206. 6): 125–126.
30. de Mun ~ iz BR. Epidemiologic oral health survey of Argentine 47. Lang NP, Scha €tzle MA, Lo € e H. Gingivitis as a risk factor in
children. Community Dent Oral Epidemiol 1985: 13: 328– periodontal disease. J Clin Periodontol 2009: 36(Suppl. 10):
333. 3–8.
̈
31. Darveau RP. Periodontitis: a polymicrobial disruption of 48. Loe H, Silness J. Periodontal disease in pregnancy. Acta
host homeostasis. Nat Rev Microbiol 2010: 8: 481–490. Odontol Scand 1963: 21: 533–551.
32. Deas DE, Mealey BL. Response of chronic and aggressive 49. Lo pez A, Lopez L, Galvez A, Rodulfo A. Diagnostico de sa-
periodontitis to treatment. Periodontol 2000 2010: 53: lud bucodental en Panama 2008. Panama. Instituto Con-
154–166. memorativo Gorgas de Estudios de la Salud 2010: 1–187.
33. Demmer RT, Papapanou PN. Epidemiologic patterns of 50. Lo pez NJ, Rıos V, Pareja MA, Ferna ndez O. Prevalence of
chronic and aggressive periodontitis. Periodontol 2000 juvenile periodontitis in Chile. J Clin Periodontol 1991: 18:
2010: 53: 28–44. 529–533.
34. Feldens EG, Kramer PF, Feldens CA, Ferreira SH. Distribu- 51. Lo pez R, Fernandez O, Jara G, Baelum V. Epidemiology of
tion of plaque and gingivitis and associated factors in 3- to clinical attachment loss in adolescents. J Periodontol 2001:
5-year-old Brazilian children. J Dent Child (Chic) 2006: 73: 72: 1666–1674.
4–10. 52. Lo pez R, Fernandez O, Jara G, Baelum V. Epidemiology of
35. Ford PJ, Gamonal J, Seymour GJ. Immunological differ- necrotizing ulcerative gingival lesions in adolescents. J
ences and similarities between chronic periodontitis and Periodontal Res 2002: 37: 439–444.
aggressive periodontitis. Periodontol 2000 2010: 53: 53. Lo pez R, Baelum V. Classifying periodontitis among ado-
111–123. lescents: implications for epidemiological research. Com-
36. Freire Mdo C, Reis SC, Goncßalves MM, Balbo PL, Leles CR. munity Dent Oral Epidemiol 2003: 31: 136–143.
Oral health in 12 year-old students from public and pri- 54. Maltz M, Barbachan e Silva B. Relationship among caries,
vate schools in the city of Goia ^nia, Brazil. Rev Panam Sa- gingivitis and fluorosis and socioeconomic status of school
lud Publica 2010: 28: 86–91. children. Rev Saude Publica 2001: 35: 170–176.
37. Galvez CA, Rodulfo A, Iba n
~ ez D, Chavez D, Brown L, De 55. Maltz M, Schoenardie AB, Carvalho JC. Dental caries and
Lacerda A, Ricco R, Noriega MC, Caballero N, Lopez A, gingivitis in schoolchildren from the municipality of Porto
Lopes L, Chang N, Crespo MV. Diagnostico de la salud Alegre, Brazil in 1975 and 1996. Clin Oral Investig 2001: 5:
bucodental en Panama (DISABU 2008). El Odontol 2008: 199–204.
27: 17–23. 56. Martinez J. La odontologia en America Latina, en numeros.
38. Gjermo P, Ro €sing CK, Susin C, Oppermann RV. Periodon- Dent Trib 2011. [WWW document]. URL http://www.dental-
tal diseases in Central and South America. Periodontol tribune.com/articles/content/scope/news/region/hispanic/
2000 2002: 29: 70–78. id/6623#.TrP68hgRbX4.email [Accessed 11 April 2011].
39. Go mez-Restrepo AM, Ardila-Medina CM, Franco-Cortes 57. Massler M, Schour I, Chopra B. Occurrence of gingivitis in
AM, Duque-Agudelo L, Osorno-Cardona C, Moros-Reyes suburban Chicago school children. J Periodontol 1950: 21:
A, Guzma n-Zuluaga IC. Risk indicators for clinical attach- 146–164.
ment loss among adolescents from public schools in 58. Medina C, Cerrato JA, Herrera MS. Perfil epidemiolo  gico
Medellin, Colombia. Clin Periodoncia Implantol Rehabil de la caries dental y enfermedad periodontal, en Nicara-
Oral 2008: 1: 23–26. gua, an~ o 2005. Universitas 2007: 1: 39–46.
40. Guerreiro PO, Garcias Gde L. Oral health conditions diag- 59. Ministe rio da Sau de. Projeto SB Brasil. Condicßo~ es de sau de
nostic in cerebral palsy individuals of Pelotas, Rio Grande bucal da populacßa ~o brasileira 2002-2003, 2003. Resultados
do Sul State, Brazil. Cien Saude Colet 2009: 14: 1939–1946. Principais. URL: http://cfo.org.br/wp-content/uploads/
41. Guimara ~es MC, de Arau  jo VM, Avena MR, Duarte DR, Fre- 2009/10/04_0347_M.pdf [Accessed 12 September 2011].
itas FV. Prevalence of alveolar bone loss in healthy chil- 60. Ministerio de Salud Publica. Estudio epidemimologico de
dren treated at private pediatric dentistry clinics. J Appl salud bucal en escolares del Ecuador. OPS 1988: 1–35.
Oral Sci 2010: 18: 285–290. URL:http://new.paho.org/hq/index.php?option=com_con

55
Botero et al.

tent&task=view&id=1158&Itemid=259 [Accessed 12 Octo- 78. Quin ~o nez ME, Rodrıguez A, Gonza lez B, Padilla C. Morbili-
ber 2011]. dad bucal: Su relacio n con el estado nutricional en nin ~ os
61. Ministerio de Salud y Bienestar Social. Repu  blica de Para- de 2 a 5 an ~ os de la Consulta de Nutricio  n del Hospital
guay. Encuesta Nacional sobre Salud Oral. OPS Parag Pedia trico Docente de Centro Habana. Rev Cubana Esto-
2008: 1–91. http://new.paho.org/hq/index.php?option=com_ matol 2004: 41. URL: http://scielo.sld.cu/scielo.php?
content&task=view&id=1171&Itemid=259 [Accessed 6 script=sci_arttext&pid=S0034-75072004000100001&lng=es
October 2011]. [Accessed 26 September 2011].
62. MINSAL. Perfil epidemiolo  gico de salud bucal. URL: www. 79. Quin ~ onez ME, Ferro PP, Valdes H, Cevallos J, Rodrıguez A.
minsal.gob.cl/. . ./7dc33df0bb34ec58e04001011e011c36.pdf Relacio n de afecciones bucales con el estado nutricional
[Accessed 12 September 2011]. en escolares de primaria del municipio Bauta. Rev Cubana
63. Moreno M, Esper ME. Periodontitis incipiente en adole- Estomatol 2006: 43. URL: http://scielo.sld.cu/scielo.php?
scentes de 14 a 18 an ~ os. Revista claves de Odontologıa script=sci_arttext&pid=S0034-75072006000100004&lng=es
2003: 52: 65–68. [Accessed 26 September 2011].
64. Murrieta JF, Juarez LA, Linares C, Zurita V. Prevalencia de 80. Quin ~ ones ME, Lisbeth PP, Ferro PP, Martınez H, Santana S.
gingivitis en un grupo de escolares y su relacio  n con el gra- Estado de salud bucal: su relacio n con el estado nutricional
do de higiene oral y el nivel de conocimientos sobre salud en nin ~ os de 2 a 5 an ~ os. Rev Cubana Estomatol 2008: 45.
bucal demostrado por sus madres. Bol Med Hosp Infant URL: http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=
Mex 2004: 61: 44–54. S003475072008000200004&lng=es [Accessed 26 September
65. Navaz R, Rojas T, Zambrano O, Alvarez C, Santana Y, Viera 2011].
N. Salud bucal en preescolares: su relacion con las acti- 81. Ramfjord SP. Indices for prevalence and incidence of peri-
tudes y nivel educativo de los padres. Interciencia 2002: 27: odontal disease. J Periodontol 1959: 30: 51–59.
631–634. 82. Rebelo MA, Lopes MC, Vieira JM, Parente RC. Dental car-
66. Nicolau B, Marcenes W, Hardy R, Sheiham A. A life-course ies and gingivitis among 15 to 19 year-old students in
approach to assess the relationship between social and Manaus, AM, Brazil. Braz Oral Res 2009: 23: 248–254.
psychological circumstances and gingival status in adoles- 83. Repu  blica de Colombia. Ministerio de Salud. Estudio
cents. J Clin Periodontol 2003: 30: 1038–1045. Nacional de Salud Bucal. Serie Documentos Tecnicos,
67. Nogueira dos Santos NC, Alves TD, Freitas VS, Jamelli SR, Tomo VII. Bogota : Repu  blica de Colombia. Ministerio de
Cavalcanti Sarinho ES. Oral health among adolescents: Salud, 1999.
aspects relating to hygiene, dental cavities and periodontal 84. Ribeiro Ade A, Portela M, Souza IP. Relation between bio-
disease in the cities of Recife and Feira de Santana, Brazil. film, caries activity and gingivitis in HIV+ children. Pesqui
Cien Saude Colet 2007: 12: 1155–1166. Odontol Bras 2002: 16: 144–150.
68. Nowzari H, Botero JE. Latin America: native populations 85. Rivera MCA. Pre-school child oral health in a rural Chilean
affected by early onset periodontal disease. J Calif Dent community. Int J Odontostomat 2011: 5: 83–86.
Assoc 2011: 39: 383–391. 86. Russell AX. A system of classification and scoring for prev-
69. Ocampo D, Ba ez R. Estudio epidemiolo  gico de salud bucal alence surveys of periodontal disease. J Dent Res 1956: 35:
1995. Bolivia. OPS 1997: 1–65. 350–359.
70. Offenbacher S, Barros SP, Singer RE, Moss K, Williams RC, 87. Scha€tzle M, Lo € e H, Bu€ rgin W, Anerud A, Boysen H, Lang
Beck JD. Periodontal disease at the biofilm-gingival inter- NP. Clinical course of chronic periodontitis. I. Role of gin-
phase. J Periodontol 2007: 78: 1911–1925. givitis. J Clin Periodontol 2003: 30: 887–901.
71. Oh TJ, Eber R, Wang HL. Periodontal diseases in the child 88. SIVEPAB. Resultados del Sistema de Vigilancia Epidemi-
and adolescent. J Clin Periodontol 2002: 29: 400–410.  gico de Patologıas Bucales SIVEPAB 2010. Primera Ed.
olo
72. Orozco AH, Franco AM, Ramirez-Yan ~ ez GO. Periodontal 2011. URL: http://www.cenavece.salud.gob.mx/progra-
treatment needs in a native island community in Colom- mas/interior/saludbucal/vigilancia/index.html [Accessed
bia determined with CPITN. Int Dent J 2004: 54: 73–76. 23 May 2012].
73. Orozco RE, Peralta H, Palma GG, Perez E, Arroniz S, Lla- 89. Smith M, Seymour GJ, Cullinan MP. Histopathological fea-
mosas E. Prevalencia de gingivitis en adolescentes en el tures of chronic and aggressive periodontitis. Periodontol
municipio de Tlalnepantla. Rev ADM 2002: 59: 16–21. 2000 2010: 53: 45–54.
74. Ortega M, Mota V, Lo  pez JC. Oral health status of adoles- 90. Soto L, Tapia R, Jara G, Rodrıguez G, Urbina T, Venegas
cents in Me xico City. Rev Salud Publica 2007: 9: 380–387. C, Cabello R, Godoy E, Becar P, Gamboa F, Aranda W,
75. Page RC, Eke PI. Case definitions for use in population Baez RJ, Martinez B. Diagno  stico Nacional de Salud Bu-
based surveillance of periodontitis. J Periodontol 2007: 78: cal del Adolescente de 12 an ~ os y Evaluacio  n del Grado
1387–1399. de Cumplimiento de los Objetivos Sanitarios de Salud
76. Papapanou P, Wennstro €m J, Johnsson T. Extent and sever- Bucal 2000-2010. Facultad de Odontologıa. Ediciones
ity of periodontal destruction based on partial clinical Universidad Mayor. Serie Documentos Te cnicos 2007:
assessments. Community Dent Oral Epidemiol 1993: 21: 50-54.
181–184. 91. Susin C, Haas AN, Oppermann RV, Haugejorden O, Alban-
77. Peres MA, Peres KG, Cascaes AM, Correa MB, Demarco FF, dar JM. Gingival recession: epidemiology and risk indica-
Hallal PC, Horta BL, Gigante DB, Menezes AB. Validity of tors in a representative urban Brazilian population. J
partial protocols to assess the prevalence of periodontal Periodontol 2004: 75: 1377–1386.
outcomes and associated socio demographic and behavior 92. Susin C, Albandar JM. Aggressive periodontitis in an urban
factors in adolescents and young adults. J Periodontol population in southern Brazil. J Periodontol 2005: 76:
2012: 83: 369–378. 468–475.

56
Periodontal disease in Latin American children and adolescents

93. Susin C, Haas AN, Valle PM, Oppermann RV, Albandar JM. dentition: a retrospective follow-up study. Pediatr Dent
Prevalence and risk indicators for chronic periodontitis in 2011: 33: 312–315.
adolescents and young adults in south Brazil. J Clin Peri- 98. World Health Organization Collaborating Center. Oral
odontol 2011: 38: 326–333. health. Periodontal country profiles [WWW document].
94. Taboada O, Talavera I. Prevalence of gingivitis in pre- Japan: World Health Organization Collaborating Center
school-age children living on the east side of Mexico City. Niigata University Graduate School of Medical and Dental
Bol Med Hosp Infant Mex 2011: 68: 21–25. Sciences. URL http://www.who.int/oral_health/databas-
95. Triana FE, Rivera SV, Soto L, Bedoya A. Estudio de morbili- es/niigata/en/index.html [Accessed 21 February 2012].
dad oral en nin~ os escolares de una poblacio n de indıgenas 99. World Health Organization. World Health Statistics
amazo nicos. Colomb Med 2005: 36(Suppl. 3): 26–30. 2012. WHO 2012:124-126. URL http://www.who.int/gho/
96. Varas F, Zillmann G, Munnoz A, Hassi J. Estado periodon- publications/world_health_statistics/2012/en/index.html
tal y necesidades de tratamiento en nin ~ os de 6 a 8 an
~ os de [Accessed 21 May 2012].
edad de la Regio  n Metropolitana. An~ o 2004-2006. Rev Soc 100. Schour I, Massler M. Gingival disease in postwar Italy
Chil Odontopediatrıa 2008: 23: 9–10. (1945) prevalence of gingivitis in various age groups. J Am
97. Vizzoto MB, Rosing CK, Araujo FB, Silveira HED. Radio- Dent Assoc 1947: 35: 475–482.
graphic evaluation of alveolar bone height in the primary

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