Professional Documents
Culture Documents
Acne and Diet A Sistematic Review 2022 1
Acne and Diet A Sistematic Review 2022 1
Background: Acne vulgaris is a common cutaneous disorder. Diet and metabolism, specifically glycemic
content and dairy, influence hormones such as insulin, insulin-like growth factor 1, and androgens, which
affect acnegenesis.
Objective: To systematically review high-quality evidence regarding the association of dietary glycemic
and dairy intake with acnegenesis.
Results: The literature search yielded 410 articles, of which 34 articles met the inclusion criteria. The
literature on whether dairy product intake is associated with acnegenesis is mixed and may be dependent
on sex, ethnicity, and cultural dietary habits. High glycemic index and increased daily glycemic load intake
were positively associated with acnegenesis and acne severity, an observation supported by randomized
controlled trials.
Conclusion: High glycemic index, increased glycemic load, and carbohydrate intake have a modest yet
significant proacnegenic effect. Increased dairy consumption may have been proacnegenic in select
populations, such as those in which a Western diet is prevalent. The impact of diet on acnegenesis is likely
dependent on sex and ethnicity. Further randomized trials are necessary to fully characterize the potential
associations. ( JAAD Int 2022;7:95-112.)
Key words: acne; diet; dairy; glycemic index; randomized control trial; sugar.
From the Solomon H. Snyder Department of Neuroscience,a and Correspondence to: Byron K. Ho, MD, Department of Dermatology,
Department of Dermatology, Johns Hopkins University School Johns Hopkins University School of Medicine, 601 N Caroline
of Medicine, Baltimore, Marylandb; and Robert Wood Johnson Street, JHOC 8072, Baltimore, MD 21287. E-mail: bho8@jhmi.
Medical School, Rutgers University, Piscataway, New Jersey.c edu.
Dr Meixiong and Ms Ricco contributed equally to this article. 2666-3287
Funding sources: Supported by NIH T32 GM136577 (to C.V. and Ó 2022 by the American Academy of Dermatology, Inc. Published
J.M.). by Elsevier Inc. This is an open access article under the CC
IRB approval status: This review was exempt from regulation by BY-NC-ND license (http://creativecommons.org/licenses/by-nc-
the Johns Hopkins School of Medicine Institutional Review nd/4.0/).
Board. https://doi.org/10.1016/j.jdin.2022.02.012
Accepted for publication February 25, 2022.
95
96 Meixiong et al JAAD INT
JUNE 2022
implicated in acne pathogenesis. GI is a 1-100 their acne. Accordingly, the interest in the topic has
scoring system used to determine how quickly car- increased in recent years, and new studies are
bohydrate content is digested, absorbed, and metab- constantly being added to the literature.13,14 Here,
7
olized. In multiple clinical trials, high-GI diets ([55) we present a review of the high-quality evidence of
have been associated with worse glycemic control, the relationship between acne and dairy and be-
higher postprandial insulin levels,7,8 and elevated tween acne and sugar/glycemic content to draw
insulin-like growth factor 1 (IGF-1) levels,7 whereas more accurate conclusions from a variety of data.
low-GI diets have been Dozens of dietary compo-
shown to decrease fasting nents, ranging from specific
IGF-1 concentrations.9-11 CAPSULE SUMMARY micronutrients to entire
Similarly, frequent dairy con- macronutrient classes, have
sumers have higher serum d
The effect of diet on acne has been of been proposed to both posi-
levels of IGF-1 and insulin interest for many years, and we present tively and negatively affect
compared with nondairy an update of the evidence of the effect acne. In contrast to other
consumers,12,13 and the of glycemic index/load and dairy on excellent, published reviews
ingestion of either whey or acne. of these foodstuffs, we limit
casein, protein dairy compo- d We provide a succinct reference by our focus here to dairy and
nents, has been associated which providers can advise their patients glycemic content because
with increased levels of IGF- with acne on the effect of dietary habits. the biochemical pathways
1 and insulin.14-17 Notably, a by which they can alter
2-year randomized control acne-pathogenic hormones
trial (RCT) examining whey protein ingestion and have been clearly delineated.
bone health in postmenopausal women determined
that high whey consumption resulted in higher METHODS
serum IGF-1 levels, 7.3% at 1 year and 8% at 2 years.18 We conducted a comprehensive literature search,
Numerous ethnographic observational studies without timeline restriction, of the MEDLINE database
have noted lower acne prevalence among non- according to the 2020 Preferred Reporting Items for
Westernized peoples.7-11 In 1 notable study, the Systematic Reviews and Meta-Analyses guidelines.15
members of 2 South American indigenous peoples, The literature search, article identification and selec-
the Kitavans of Papua New Guinea and the Ache of tion, data extraction and analysis, and manuscript
Paraguay, were followed-up. In contrast to Western screening were performed between October and
diets, both the groups adhered to low-GI diets November 2021. The last literature search was per-
consisting of fish, wild game, tubers, and foraged formed on October 4, 2021. Our search terms
foods and consumed almost no dairy, alcohol, cof- included ‘‘Acne AND dairy,’’ ‘‘Acne AND milk,’’
fee, tea, oils, sugar, and salt. After many months of ‘‘Acne AND whey,’’ ‘‘Acne AND glycemic,’’ ‘‘Acne
observation, the researchers found no cases of acne AND sugar,’’ and ‘‘Acne AND carbohydrate,’’ yielding
among adolescents or adults.19 Interestingly, genet- a total combined number of 410 articles.
ically similar Pacific Islanders and South American Two reviewers independently screened the titles,
Indians who have adopted a more Westernized abstracts, and full text to determine whether they met
lifestyle have much higher incidences of acne. the inclusion criteria detailed in Fig 1. The inclusion
Similar trends were observed among other peoples, criteria were as follows: (1) primary observational
such as Okinawans and the Inuit, in whom the acne and interventional studies of participants with acne;
prevalence increased after the adoption of a Western (2) a survey/questionnaire/interview assessment of
lifestyle.9,12 These comparisons suggest that envi- eating habits or specific dietary interventions; and (3)
ronmental factors present in a rural, nonindustrial- outcomes examining the association of acne with GI,
ized lifestyle protect people from the development glycemic load, and/or dairy products. We excluded
of acne. Alternatively, an industrialized lifestyle, non-English papers, meta-analyses, case reports,
specifically, the adoption of a Western diet, high in case series, systematic and general reviews,
sugar/glycemic and dairy content, may be Mendelian randomizations, semantic connectivity
proacnegenic. map approaches, commentaries, and articles that
Based on these observations, many research were not accessible for the full-text review.
groups have considered whether the intake of dairy Data extraction for pertinent variables (study
or high-GI foods has a role in modulating acne design, participant characteristics, methods/inter-
development and severity; moreover, patients them- vention, outcome, and the level of evidence [LOE])
selves often ask whether changes in diet can improve was conducted by J.M., C.R., C.V., and B.K.H. The
JAAD INT Meixiong et al 97
VOLUME 7
Abbreviations used:
IGF-1: insulin-like growth factor 1
GI: glycemic index
LOE: level of evidence
RCT: randomized control trial
98 Meixiong et al
Study design; no. of Participant Quality of
Source; country participants characteristics Measures Outcome summary Strengths Limitations evidence
Bett et al,20 1967; Case-control 15-27 y olds recruited Questionnaire on No significant Well-defined case Low sample size. 5
United Kingdom study; 16 from 2 clinics. Age/ daily sugar intake. difference in daily selection. Potential bias in
patients with sex-matched Physician-diagnosed sugar intake Appropriate control exposure
acne, 29 controls recruited acne. between patients selection. classification
controls from a clinic and a with acne and
factory/office. controls.
Kaymak et al,19 Case-control 19-34 y olds recruited Questionnaire on the No significant Well-defined case Low sample size. 7
2007; Turkey study; 49 from outpatient frequency of food difference in GI selection. Potential bias in
patients with clinics. consumption and between patients Appropriate control exposure
acne, 42 dietary intake. with acne and selection. classification
controls Dermatologist- controls. No
assessed acne significant
severity. difference in
glycemic load
between patients
with acne and
controls.
Koku Aksu et al,21 Cross-sectional 13-18-y-old Questionnaire on Frequent sugar intake Appropriate sample Potential biases in 7
2011; Turkey study; 2230 adolescents from dietary intake and (aOR, 1.3 [1.06- size. Unbiased outcome
multiple schools. personal history of 1.82]) and frequent exposure classification
acne. sweet consumption classification.
Dermatologist- (aOR 1.2 [1.16-1.43])
evaluated acne associated with
severity (Pillsbury acne.
diagnostic criteria).
Burris et al,22 2017; Cross-sectional 18-40 y olds with Dietician-instructed Moderate/severe acne Well-defined outcome Low sample size. 7
New York City study; 64 moderate/severe 5-d food and group had a higher classification. Potential bias in
and no acne beverage record. glucose load than Unbiased exposure recruitment.
recruited by Dermatologist- participants classification.
advertising. evaluated acne without acne
severity. Bloodwork (137 6 41 vs
at study conclusion. 117 6 41,
respectively;
P \ .001). No
association
between GI and
JAAD INT
JUNE 2022
acne.
VOLUME 7
JAAD INT
Huang et al,23 Cross-sectional 18-19-y-old students Questionnaire on Soft drink sugar Appropriate sample Potential bias in 7
2019; China study; 8197 from 353 cities. dietary intake. intake $100 g/d size. Well-defined exposure
Dermatologist- significantly case selection. classification.
assessed acne associated with
history and severity moderate-to-severe
(Pillsbury acne (aOR 3.12
diagnostic criteria). [1.80-5.41]).
Meixiong et al 99
milk not associated.
Adebamowo Retrospective 9-15-y-old girls from Questionnaires on Whole, low-fat, skim, Appropriate sample Potential bias in 5
et al,25 2006; cohort study; GUTS. food consumption or chocolate milk size. Longitudinal, outcome
United States 6094 frequency and the associated with generalized classification.
self-assessment of acne in 1996. PRs exposure
the presence and ranged from 1.17 classification.
severity of acne. (1.04-1.31) to 1.29
(1.08-1.53).
Continued
Table II. Cont’d
100 Meixiong et al
Study design; no. of Participant Quality of
Source; country participants characteristics Measures Outcome summary Strengths Limitations evidence
Adebamowo Retrospective 9-15-y-old boys from Questionnaires on Skim milk associated Appropriate sample Potential bias in 4
et al,26 2008; cohort study; GUTS. food consumption with acne (PR 1.19 size. Longitudinal, outcome
United States 4273 frequency and the [1.01-1.40]). Total generalized classification.
self-assessment of milk, whole milk, exposure Multiple testing
the presence and 2% milk, and low- classification. bias.
severity of acne. fat milk not
associated.
Di Landro et al,27 Case-control 10-24 y olds from 15 Questionnaire on the Milk consumption Appropriate sample None. 9
2012; Italy study; 205 different outpatient frequency of ([3 portions per size. Multiple
patients with hospital clinics. dietary intake. wk) associated with institutions. Well-
acne, 358 Dermatologist- moderate-to-severe defined outcome
controls evaluated acne acne (OR 1.78 [1.22- classification.
severity (global 2.59]). Unbiased study
acne assessment recruitment.
scale). Generalized
exposure
classification.
Pontes et al,28 Longitudinal 18-30 y olds with Dermatologist- Protein calorie Well-defined Low sample size. 6
2013; Brazil cohort study; 30 recent protein assessed acne supplementation exposure and Potential
calorie (Leeds) before, after significantly outcome recruitment bias.
supplementation 30 d, and after 60 d increased comedo classification.
use from of protein-calorie and acne lesion
dermatology clinics supplementation. count.
and gyms.
Semedo et al,29 Cross-sectional 20-60 y olds from 5 Questionnaire on Reduced-fat milk and Appropriate sample None. 8
2016; Portugal study; 1055 different clinics. dietary intake. whole milk size. Multiple
Dermatologist- consumption institutions. Well-
evaluated acne associated with defined outcome
(Pillsbury). acne (OR 1.33 [1.03- classification.
1.70]). Unbiased study
recruitment.
Generalized
exposure
classification.
JAAD INT
JUNE 2022
VOLUME 7
JAAD INT
Duquia et al,30 Cross-sectional 18-y-old enlisted men. Questionnaire (Y/N) No significant Appropriate sample Generalizability. 6
2017; Brazil study; 2201 on daily cheese, association size. Unbiased Limited exposure
whole milk, low-fat between acne and recruitment. classification in Y/N
milk, and yogurt milk was found. format. No severity
consumption. grading.
Dermatologist-
evaluated acne.
Ulvestad et al,31 Longitudinal 15-16-y-old (10th Questionnaire on High intake of full-fat Appropriate sample Potential bias in 6
2017; Norway cohort study; grade) Norwegian dairy consumption dairy associated size. Unbiased exposure and
2489 students. at baseline and the with acne (OR 1.56 recruitment. outcome
presence of acne [1.02-2.39]). Total classification.
after 3 y. milk intake in girls Generalizability.
only associated
with acne (OR 1.80
[1.02-3.16]).
Heng et al,32 2022; Cross-sectional 17-71 y olds from a Questionnaire on diet. Frequent milk Appropriate sample Potential bias in 7
Singapore study; 2090 clinic. Trained personnel consumption size. Well-defined exposure
cases and 1798 evaluated the associated with a outcome classification.
controls presence, severity, lower likelihood of classification.
and scarring of moderate-to-severe
acne lesions. acne (OR 0.572
[0.360-0.910]).
Say et al,33 2021; Cross-sectional 17-77 y olds from 2 Questionnaire on diet. No association Appropriate sample Potential bias in 7
Singapore study; 1117 different hospital Medical staff between the size. Well-defined exposure
patients with sites. evaluated the frequency of milk outcome classification.
acne and 723 presence, severity, consumption and classification.
controls and scarring of acne severity.
acne lesions. Increased milk
consumption
associated with a
lower risk of
scarring.
GUTS, Growing Up Today Study; OR, odds ratio; PR, prevalence ratio.
*Negative studies - Say et al58 and Heng et al56 specifically asked about dairy and, therefore, had a potential bias in exposure classification. However, their results appear well supported, with hints
Meixiong et al 101
that different populations and cultural attitudes toward food consumption influence the role of diet and acne.
Table III. Observational studies on the effect of both glycemic index/glycemic load and dairy on acne
102 Meixiong et al
Study design; no. of Participant Quality of
Source; country participants characteristics Measures Outcome summary Strengths Limitations evidence
Ismail et al,34 Case-control 18-30 y olds from a Interview on the High glycemic load Appropriate sample Unrepresentative 6
2012; study; 44 dermatology clinic frequency of milk (175 6 35 in size. Well-defined control selection
Malaysia patients with (with acne) and a consumption and patients with acne case selection and (university student).
acne, 44 university campus 3-d food diary. vs 122 6 28 in exposure
controls (control). Dermatologist- controls), milk (OR classification.
evaluated acne 3.99 [1.39-11.43]),
severity and ice cream (OR
(comprehensive 4.47 [1.77-11.266])
acne severity scale). consumption
associated with
acne.
Burris et al,35 Cross-sectional 18-25 y olds from Questionnaire on Higher GI (51.8 6 3 vs None. Low sample size. 4
2014; New study; 248 ‘‘public locations’’ dietary intake. Self- 48.9 6 4.6) and Potential
York City in New York. reported acne daily milk servings recruitment bias.
severity. (0.7 6 0.7 vs Potential biases in
0.3 6 0.5) exposure (limited)
associated with and outcome
acne severity. classification (self-
report).
Wolkenstein Cross-sectional 15-24 y olds from a Questionnaire on Daily consumption of Appropriate sample Potential recruitment 7
et al,36 2015; study; 1375 national French dietary habits and chocolate and size. Generalized bias. Potential bias
France patients with database who self- acne severity. sweets associated exposure in outcome
acne, 891 reported acne with acne (OR 2.38 classification. classification (self-
control patients status. [1.31-4.31]). Dairy report).
and sugary drink
consumption not
associated.
LaRosa et al,37 Case-control 14-19 y olds from Structured telephone Increased servings of Appropriate case and Low sample size. 6
2016; United study; 120 dermatology and interviews low-fat/skim milk control selection.
States patients with pediatric clinics. assessing 24-h (0.61 vs 0.41) in Well-defined
moderate facial dietary recall. moderate acne exposure and
acne, 105 Dermatologist- cases compared outcome
controls evaluated facial with those in acne- classification.
acne (global acne free controls.
assessment scale). Glycemic load not
associated.
JAAD INT
JUNE 2022
VOLUME 7
JAAD INT
Çerman et al,38 Case-control Participants (mean Self-reported dietary GI (47.24 6 6.6 for Well-defined Low sample size. Low 5
2016; Turkey study; 50 age: 18.8 y) intake over 1 wk. patients with acne exposure and effect size.
patients with recruited from a GL and GI and 44.52 6 6.58 outcome Unrepresentative
acne, 36 dermatology calculated using a for controls) and GL classification. control selection
controls outpatient clinic. dietary analysis increased in (hospital
software. patients with acne. volunteer).
Dermatologist- Milk consumption
assessed acne not associated.
severity.
Okoro et al,39 Cross-sectional Secondary school Interview on dietary Daily milk Well-defined Low sample size. 8
2016; Nigeria study; 464 students (mean habits and consumption exposure and
age: 13.6 y) questionnaire on (72.6% cases vs outcome
recruited from 4 food frequency. 62.0% controls) and classification.
sites. Dermatologists cake (77.8% cases
evaluated the vs 62.3% controls)
presence of acne. associated with
acne.
Suppiah et al,40 Case-control 14 y or older recruited Questionnaires on Milk (OR 2.19 [1.04- Appropriate sample Limited exposure 5
2018; study; 57 from a single dietary habits. 4.65]) and size. Appropriate classification (Y/N
Malaysia patients with hospital clinic. Dermatologist- chocolate (OR 2.4 case and control format).
acne, 57 control assessed acne [1.08-5.33]) selection. Well-
patients (comprehensive consumption defined outcome
acne severity scale). associated with classification.
acne.
Aalemi et al,41 Case-control 10-24 y olds from a Questionnaire on Whole milk (OR 2.36 Appropriate sample None. 8
2019; study; 279 single dermatology food consumption. [1.39-4.01]) and size. Appropriate
Afghanistan patients with clinic. Dermatologist- low-fat milk case and control
acne, 279 evaluated facial consumption (OR selection. Well-
controls acne (global acne 1.95 [1.10-3.45]) defined outcome
assessment scale). associated with and exposure
acne severity. classification.
Chocolate
associated with
acne.
Meixiong et al 103
Continued
Table III. Cont’d
104 Meixiong et al
Study design; no. of Participant Quality of
Source; country participants characteristics Measures Outcome summary Strengths Limitations evidence
et al,42
Karadag Case-control 12-31 y olds from 26 Questionnaire on Chocolate associated Appropriate sample None. 9
2019; Turkey study; 3826 different clinics. eating frequency with acne (OR 1.48 size. Multiple
patients with Control subjects and habits. [1.24-1.76]). Milk institutions.
acne, 759 had no record of Dermatologist- and cheese not Appropriate case
controls past or present evaluated acne associated (OR 1.13 and control
acne. severity (global [0.94-1.36]). selection. Well-
acne assessment defined exposure
scale) and outcome
classification.
Akpinar Kara Case-control 13-44 y olds from Interview on the Cheese associated Appropriate case and Low sample size. 7
and study; 53 dermatology, frequency and with acne (P \ .05). control selection.
Ozdemir,43 patients with nutrition, and quantity of food No association Well-defined
2020; Turkey acne, 53 dietetics clinics at a consumed over 3 d. found with other exposure and
controls single hospital. Dermatologist- dairy products. outcome
evaluated facial Increased classification.
acne (global acne carbohydrates
assessment scale). correlated with
acne severity
(correlation
coefficient 0.36;
P \ .01).
Dreno et al,44 Cross-sectional 15-39 y olds recruited Questionnaire on Dairy (OR 1.21 [1.1- Appropriate sample Potential recruitment 6
2020; France, study; 2826 from the internet. personal nutritional 1.35]), whey protein size. Appropriate bias. Limited
Germany, participants habits and the (OR 3.94 [3.29- case and control exposure
Italy, Brazil, with acne and presence of 4.71]), and high-GI selection. classification (Y/N).
Canada, and 3853 control clinically confirmed food consumption Potential bias in
Russia patients. acne. associated with outcome
acne. classification (self-
report).
Penso et al,45 Cross-sectional Participants (mean Questionnaire on Fatty and sugary Appropriate sample Potential recruitment 5
2020; France study; 24,452 age: 57 y); 75% food intake at products (aOR 1.54 size. Longitudinal bias. Potential
women and 25% baseline and every [1.09-2.16]), sugary exposure biases in outcome
men) from the 6 mo. Self-reported beverages (aOR classification. classification (self-
French NutriNet- acne presence and 1.18; [1.01-1.38]), report). Significant
Sante study. severity. and milk products demographic
(aOR 1.12; [1.00- differences in
JAAD INT
JUNE 2022
1.25]) associated comparison
with acne. groups.
JAAD INT Meixiong et al 105
VOLUME 7
classification.
Well-defined
associated with
acne presence,
Penso et al.45
(comprehensive
evaluated acne
Questionnaire on
Dermatologist-
106 Meixiong et al
Source; country Design Study population Intervention Control Outcome summary Strengths Limitations
47
Smith et al, 2007; Randomized 15-25-y-old males 12-wk LGL or Control group LGL diet decreased Appropriate sample Generalizability
Australia control trial (n = 43) with mild- control diet. instructed to eat total lesion count size. Rigorous (young adult
to-moderate acne carbohydrate- ( 22.0 6 3.5 for dietary compliance males).
for [6 mo recruited dense foods LGL vs 10.9 6 2.9 measures (phone
from a university. (moderate-to-high for control, P = .02) calls, daily intake,
Excluded if GL) daily but were and inflammatory urea samples, and
consuming acne or not informed about lesion count food weights).
glucose GI. ( 16.2 6 2.9 for Significant
metabolism LGL vs 5.6 6 2.5 exposure
medications. for control, P = .01). differences
Encouraged the use achieved for both
of skin cleansers. GI (low GI 43 vs
high GI 56) and GL
(low GI 101 vs high
GI 171). Well-
defined outcome
classification
(dermatologist-
assessed acne).
Smith et al,48 2007; Randomized See above. See above. See above. Reduced See above. Generalizability
Australia control trial inflammatory lesion (young adult
counts in LGL diet males). Appears
( 16.0 [ 20.6 to to be reanalyzed
11.4]) vs control data from above
( 8.5 [ 13.4 to trial.
3.5]), P = .04, and
did not reduce total
acne lesion count
after adjusting for
BMI.
Smith et al,49 2008; Randomized 15-25-y-old males See above. See above. LGL diet had See above. Generalizability
Australia control trial (n = 31) with mild- decreased acne (young adult
to-moderate facial lesion counts males). Appears
acne. Remainder ( 59%) compared to be reanalyzed
above. with control diet data from above
( 38%), P = .046), 2 trials.
and decreased skin
JAAD INT
JUNE 2022
oiliness mean
response score,
P = .013.
VOLUME 7
JAAD INT
Reynolds et al,50 2010; Nonrandomized Teenage boys (n = 43; 8 wk of high-GI Low-GI diet. Trend toward Appropriate sample Generalizability
Australia controlled trial average age: 16.5 y) diet. significant size. Significant (teenage boys),
recruited from association exposure more stringent
boarding schools. between acne differences exclusion
severity and low-GI achieved for both criteria
diet (score GI (low GI 51 6 1, (smoking/
0.65 6 0.14) vs high GI 61 6 2) and drinking, final
high-GI diet GL (low GI 102 6 9, examinations,
( 0.35 6 0.15), high GI 157 6 18). ‘‘dark’’ skin).
P = .15. Well-defined Less rigorous
outcome dietary
classification compliance
(dermatologist- measures
graded acne). (weekly
assessments of
weight and
diet).
Kwon et al.51 2012; Randomized 20-27 y olds (24 men, 10 wk of an LGL Control group asked LGL diet significantly Significant exposure Unclear sample
Korea controlled trial 8 women) with diet. to maintain regular improved the differences size justification.
mild/moderate diet. number and achieved for both Less rigorous
acne recruited from severity of acne GI (low GI dietary
a clinic. lesions compared 50.1 6 6.3, high GI compliance
with those at 69.5 6 2.4) and GL measure (GL
baseline ( 70.9%) (low GI and GI recorded
and in controls. 129.5 6 22.2, high at wk 2, 5, and
GI 207.2 6 23.2). 10).
Well-defined
outcome
classification
(dermatologist-
graded acne
severity).
Investigator
blinding.
Meixiong et al 107
Continued
108 Meixiong et al JAAD INT
JUNE 2022
and GI recorded
No data available
at wk 4, 8, and
Less rigorous
to judge the
intervention.
measure (GL
participants.
Limitations
compliance
glycemic load, sweets, and carbohydrate intake and
success of
12). 100%
acne, 77% (14/18) reported at least 1 item to be
dietary
dietary
positively associated with acnegenesis or acne severity.
Studies that linked glycemic content and acne had an
average LOE score of 6.5 (Tables I and III). Articles that
did not find an association had an average LOE score of
Appropriate sample
size. Well-defined
(dermatologist-
longitudinally).
5.5 (Tables I and III). Overall, 50% (2/4) of studies were
Strengths
graded acne
classification
showed acne
recommended for
to continue usual
noncomedogenic
benzoyl peroxide
Most of the observational studies cited gathered Acad Dermatol Venereol. 2011;25(8):950-954. https://doi.org/
data on multiple food items from their cases, 10.1111/j.1468-3083.2010.03896.x
6. Lolis MS, Bowe WP, Shalita AR. Acne and systemic disease. Med
controls, or cohorts. One additional limitation of Clin North Am. 2009;93(6):1161-1181. https://doi.org/10.1016/
the analyses was our classification of a study as j.mcna.2009.08.008
‘‘positive’’ if a single food item related to glycemic 7. Ratnam AV, Jayaraju K. Skin diseases in Zambia. Br J Dermatol.
content or dairy was significantly associated, even if 1979;101(4):449-453. https://doi.org/10.1111/j.1365-2133.1979.
many others in the study were not associated, which tb00025.x
8. Bechelli LM, Haddad N, Pimenta WP, et al. Epidemiological
created biases in our summary statistics toward the survey of skin diseases in schoolchildren living in the Purus
overestimation of a potential association. One Valley (Acre State, Amazonia, Brazil). Dermatologica. 1981;
notable example is that Adebamowo et al26 found a 163(1):78-93. https://doi.org/10.1159/000250144
significant association between skim milk and acne 9. Cordain L, Lindeberg S, Hurtado M, Hill K, Eaton SB, Brand-
but not between total milk, whole milk, 2% milk, or Miller J. Acne vulgaris: a disease of Western civilization. Arch
Dermatol. 2002;138(12):1584-1590. https://doi.org/10.1001/
low-fat milk and acne. archderm.138.12.1584
10. Park RG. The age distribution of common skin disorders in the
CONCLUSION Bantu of Pretoria, Transvaal. Br J Dermatol. 1968;80(11):758-
761. https://doi.org/10.1111/j.1365-2133.1968.tb11941.x
Despite the discussed limitations, we believe that
11. Verhagen AR, Koten JW, Chaddah VK, Patel RI. Skin diseases in
the discussed studies suggest that diet can affect acne Kenya: a clinical and histopathological study of 3,168 patients.
within select populations. Increased glycemic intake Arch Dermatol. 1968;98(6):577-586. https://doi.org/10.1001/
and high-GI diets promote acnegenesis and exacer- archderm.98.6.577
bate acne severity, whereas increased dairy intake 12. Steiner PE. Necropsies on Okinawans; anatomic and patho-
logic observations. Arch Pathol (Chic). 1946;42(4):359-380.
has been consistently shown to promote acnegene-
13. Conforti C, Agozzino M, Emendato G, et al. Acne and diet: a
sis only among Western populations. Additional review. Preprint. Posted online August 22, 2021. Int J Dermatol.
RCTs examining dairy intake and acne with respect https://doi.org/10.1111/ijd.15862
to ethnicity are required to define the exact 14. Dall’Oglio F, Nasca MR, Fiorentini F, Micali G. Diet and acne:
relationship. review of the evidence from 2009 to 2020. Int J Dermatol.
2021;60(6):672-685. https://doi.org/10.1111/ijd.15390
The effect of diet on acne is highly variable even
15. Page MJ, McKenzie JE, Bossuyt PM, et al. The PRISMA 2020
in an idealized study population. Observational statement: An updated guideline for reporting systematic
studies examining the relationship between diet reviews. J Clin Epidemiol. 2021;134:178-189. https://doi.org/
and acne should use longitudinal food diaries or 10.1016/j.jclinepi.2021.03.001
daily interviews to appropriately categorize expo- 16. Augustin LS, Kendall CW, Jenkins DJ, et al. Glycemic index,
glycemic load and glycemic response: an International Scien-
sure. Future RCTs must be appropriately powered to
tific Consensus Summit from the International Carbohydrate
determine moderate effect sizes. Quality Consortium (ICQC). Nutr Metab Cardiovasc Dis. 2015;
25(9):795-815. https://doi.org/10.1016/j.numecd.2015.05.005
The authors would like to acknowledge their funding
17. Silva FM, Kramer CK, Crispim D, Azevedo MJ. A high-glycemic
sources from the Johns Hopkins Department of index, low-fiber breakfast affects the postprandial plasma
Dermatology, the MSTP training grant, and the critical glucose, insulin, and ghrelin responses of patients with type 2
opinions and discussions of Drs Janelle Ho, Sewon Kang, diabetes in a randomized clinical trial. J Nutr. 2015;145(4):736-
Shawn Kwatra, Jihad Alhariri, Annie Grossberg, and other 741. https://doi.org/10.3945/jn.114.195339
faculty members. 18. Runchey SS, Pollak MN, Valsta LM, et al. Glycemic load effect
on fasting and post-prandial serum glucose, insulin, IGF-1 and
IGFBP-3 in a randomized, controlled feeding study. Eur J Clin
Conflicts of interest Nutr. 2012;66(10):1146-1152. https://doi.org/10.1038/ejcn.
None disclosed. 2012.107
19. Kaymak Y, Adisen E, Ilter N, Bideci A, Gurler D, Celik B. Dietary
REFERENCES glycemic index and glucose, insulin, insulin-like growth factor-
1. Collier CN, Harper JC, Cantrell WC, Wang W, Foster KW, I, insulin-like growth factor binding protein 3, and leptin levels
Elewski BE. The prevalence of acne in adults 20 years and in patients with acne. J Am Acad Dermatol. 2007;57(5):819-823.
older. J Am Acad Dermatol. 2008;58(1):56-59. https://doi.org/ https://doi.org/10.1016/j.jaad.2007.06.028
10.1016/j.jaad.2007.06.045 20. Bett DG, Morland J, Yudkin J. Sugar consumption in acne
2. Tan JK, Bhate K. A global perspective on the epidemiology of vulgaris and seborrhoeic dermatitis. Br Med J. 1967;3(5558):
acne. Br J Dermatol. 2015;172(suppl 1):3-12. https://doi.org/10. 153-155. https://doi.org/10.1136/bmj.3.5558.153
1111/bjd.13462 21. Koku Aksu AE, Metintas SE, Saracoglu ZN, et al. Acne:
3. Thiboutot D. Acne: hormonal concepts and therapy. Clin prevalence and relationship with dietary habits in Eskisehir,
Dermatol. 2004;22(5):419-428. https://doi.org/10.1016/j.clinder Turkey. J Eur Acad Dermatol Venereol. 2012;26(12):1503-1509.
matol.2004.03.010 https://doi.org/10.1111/j.1468-3083.2011.04329.x
4. Smit DL, de Ronde W. Outpatient clinic for users of anabolic 22. Burris J, Rietkerk W, Shikany JM, Woolf K. Differences in dietary
androgenic steroids: an overview. Neth J Med. 2018;76(4):167. glycemic load and hormones in New York city adults with no
5. Ben-Amitai D, Laron Z. Effect of insulin-like growth factor-1 and moderate/severe acne. J Acad Nutr Diet. 2017;117(9):1375-
deficiency or administration on the occurrence of acne. J Eur 1383. https://doi.org/10.1016/j.jand.2017.03.024
JAAD INT Meixiong et al 111
VOLUME 7
23. Huang X, Zhang J, Li J, et al. Daily intake of soft drinks and 38. Çerman AA, Aktaş E, Altunay _IK, Arıcı JE, Tulunay A, Ozturk FY.
moderate-to-severe acne vulgaris in Chinese adolescents. J Dietary glycemic factors, insulin resistance, and adiponectin
Pediatr. 2019;204:256-262. https://doi.org/10.1016/j.jpeds. levels in acne vulgaris. J Am Acad Dermatol. 2016;75(1):155-
2018.08.034 162. https://doi.org/10.1016/j.jaad.2016.02.1220
24. Adebamowo CA, Spiegelman D, Danby FW, Frazier AL, 39. Okoro EO, Ogunbiyi AO, George AO, Subulade MO. Associa-
Willett WC, Holmes MD. High school dietary dairy intake and tion of diet with acne vulgaris among adolescents in Ibadan,
teenage acne. J Am Acad Dermatol. 2005;52(2):207-214. https: southwest Nigeria. Int J Dermatol. 2016;55(9):982-988. https:
//doi.org/10.1016/j.jaad.2004.08.007 //doi.org/10.1111/ijd.13166
25. Adebamowo CA, Spiegelman D, Berkey CS, et al. Milk con- 40. Suppiah TS, Sundram TK, Tan ES, Lee CK, Bustami NA, Tan CK.
sumption and acne in adolescent girls. Dermatol Online J. Acne vulgaris and its association with dietary intake: a
2006;12(4):1. Malaysian perspective. Asia Pac J Clin Nutr. 2018;27(5):1141-
26. Adebamowo CA, Spiegelman D, Berkey CS, et al. Milk con- 1145. https://doi.org/10.6133/apjcn.072018.01
sumption and acne in teenaged boys. J Am Acad Dermatol. 41. Aalemi AK, Anwar I, Chen H. Dairy consumption and acne: a
2008;58(5):787-793. https://doi.org/10.1016/j.jaad.2007.08.049 case control study in Kabul, Afghanistan. Clin Cosmet Investig
27. Di Landro A, Cazzaniga S, Parazzini F, et al. Family history, Dermatol. 2019;12:481-487. https://doi.org/10.2147/CCID.S195
body mass index, selected dietary factors, menstrual history, 191
and risk of moderate to severe acne in adolescents and young 42. Karada g AS, Balta I, Saricao
glu H, et al. The effect of personal,
adults. J Am Acad Dermatol. 2012;67(6):1129-1135. https: familial, and environmental characteristics on acne vulgaris: a
//doi.org/10.1016/j.jaad.2012.02.018 prospective, multicenter, case controlled study. G Ital Derma-
28. Pontes TD, Fernandes Filho GM, Trindade AD, Sobral Filho JF. tol Venereol. 2019;154(2):177-185. https://doi.org/10.23736/
Incidence of acne vulgaris in young adult users of protein- S0392-0488.17.05532-8
calorie supplements in the city of Joao Pessoa-PB. An Bras 43. Akpinar Kara Y, Ozdemir D. Evaluation of food consumption in
Dermatol. 2013;88(6):907-912. https://doi.org/10.1590/abd patients with acne vulgaris and its relationship with acne
1806-4841.20132024 severity. J Cosmet Dermatol. 2020;19(8):2109-2113. https:
29. Semedo D, Ladeiro F, Ruivo M, et al. Adult acne: prevalence //doi.org/10.1111/jocd.13255
and portrayal in primary healthcare patients, in the Greater 44. Dreno B, Shourick J, Kerob D, Bouloc A, Taieb C. The role of
Porto Area, Portugal. Acta Med Port. 2016;29(9):507-513. https: exposome in acne: results from an international patient
//doi.org/10.20344/amp.6626 survey. J Eur Acad Dermatol Venereol. 2020;34(5):1057-1064.
30. Duquia RP, Dos Santos ID, de Almeida H Jr, Souza PR, de https://doi.org/10.1111/jdv.16119
Avelar Breunig J, Zouboulis CC. Epidemiology of acne vulgaris 45. Penso L, Touvier M, Deschasaux M, Hercberg S, Ezzedine K,
in 18-year-old male army conscripts in a South Brazilian city. Sbidian E. Association between adult acne and dietary
Dermatology. 2017;233(2-3):145-154. https://doi.org/10.1159/ behaviors: findings from the NutriNet-Sante Prospective
000475775 Cohort Study. JAMA Dermatol. 2020;156(8):854-862. https:
31. Ulvestad M, Bjertness E, Dalgard F, Halvorsen JA. Acne and //doi.org/10.1001/jamadermatol.2020.1602
dairy products in adolescence: results from a Norwegian 46. Anaba EL, Oaku IR. Adult female acne: a cross-sectional study
longitudinal study. J Eur Acad Dermatol Venereol. 2017;31(3): of diet, family history, body mass index, and premenstrual
530-535. https://doi.org/10.1111/jdv.13835 flare as risk factors and contributors to severity. Int J Womens
32. Heng AH, Say YH, Sio YY, Ng YT, Chew FT. Epidemiological risk Dermatol. 2021;7(3):265-269. https://doi.org/10.1016/j.ijwd.
factors associated with acne vulgaris presentation, severity, 2020.11.008
and scarring in a Singapore Chinese population: a cross- 47. Smith RN, Mann NJ, Braue A, Makelainen H, Varigos GA. A low-
sectional study. Dermatology. 2022;238(2):226-235. https: glycemic-load diet improves symptoms in acne vulgaris
//doi.org/10.1159/000516232 patients: a randomized controlled trial. Am J Clin Nutr. 2007;
33. Say YH, Heng AH, Reginald K, et al. Modifiable and non- 86(1):107-115. https://doi.org/10.1093/ajcn/86.1.107
modifiable epidemiological risk factors for acne, acne severity 48. Smith RN, Mann NJ, Braue A, Makelainen H, Varigos GA. The
and acne scarring among Malaysian Chinese: a cross-sectional effect of a high-protein, low glycemic-load diet versus a
study. BMC Public Health. 2021;21(1):1-12. https://doi.org/10. conventional, high glycemic-load diet on biochemical param-
1186/s12889-021-10681-4 eters associated with acne vulgaris: a randomized,
34. Ismail NH, Manaf ZA, Azizan NZ. High glycemic load diet, investigator-masked, controlled trial. J Am Acad Dermatol.
milk and ice cream consumption are related to acne vulgaris 2007;57(2):247-256. https://doi.org/10.1016/j.jaad.2007.01.046
in Malaysian young adults: a case control study. BMC 49. Smith R, Mann N, M€akel€ainen H, Roper J, Braue A, Varigos G. A
Dermatol. 2012;12(1):1-8. https://doi.org/10.1186/1471- pilot study to determine the short-term effects of a low
5945-12-13 glycemic load diet on hormonal markers of acne: a non-
35. Burris J, Rietkerk W, Woolf K. Relationships of self-reported randomized, parallel, controlled feeding trial. Mol Nutr Food
dietary factors and perceived acne severity in a cohort of New Res. 2008;52(6):718-726. https://doi.org/10.1002/mnfr.200700307
York young adults. J Acad Nutr Diet. 2014;114(3):384-392. 50. Reynolds RC, Lee S, Choi JY, et al. Effect of the glycemic index
https://doi.org/10.1016/j.jand.2013.11.010 of carbohydrates on acne vulgaris. Nutrients. 2010;2(10):1060-
36. Wolkenstein P, Misery L, Amici JM, et al. Smoking and dietary 1072. https://doi.org/10.3390/nu2101060
factors associated with moderate-to-severe acne in French 51. Kwon HH, Yoon JY, Hong JS, Jung J, Park MS, Suh DH. Clinical
adolescents and young adults: results of a survey using a and histological effect of a low glycaemic load diet in
representative sample. Dermatology. 2015;230(1):34-39. https: treatment of acne vulgaris in Korean patients: a randomized,
//doi.org/10.1159/000366195 controlled trial. Acta Derm Venereol. 2012;92(3):241-246. https:
37. LaRosa CL, Quach KA, Koons K, et al. Consumption of dairy in //doi.org/10.2340/00015555-1346
teenagers with and without acne. J Am Acad Dermatol. 2016; 52. Pavithra G, Upadya GM, Rukmini MS. A randomized controlled
75(2):318-322. https://doi.org/10.1016/j.jaad.2016.04.030 trial of topical benzoyl peroxide 2.5% gel with a low glycemic load
112 Meixiong et al JAAD INT
JUNE 2022
diet versus topical benzoyl peroxide 2.5% gel with a normal diet plasma insulin, glucagon, ghrelin, CCK, GIP, and GLP-1 re-
in acne (grades 1-3). Indian J Dermatol Venereol Leprol. 2019;85(5): sponses to whey protein ingestion. Nutrients. 2017;10(1):2.
486-490. https://doi.org/10.4103/ijdvl.IJDVL_109_17 https://doi.org/10.3390/nu10010002
53. Danby FW. Acne, dairy and cancer: the 5alpha-P link. 57. Larnkjaer A, Arnberg K, Michaelsen KF, Jensen SM, Molgaard C.
Dermatoendocrinology. 2009;1(1):12-16. https://doi.org/10. Effect of milk proteins on linear growth and IGF variables in
4161/derm.1.1.7124 overweight adolescents. Growth Horm IGF Res. 2014;24(2-3):
54. Ma J, Giovannucci E, Pollak M, et al. Milk intake, circulating 54-59. https://doi.org/10.1016/j.ghir.2013.12.004
levels of insulin-like growth factor-I, and risk of colorectal 58. Hoppe C, Molgaard C, Dalum C, Vaag A, Michaelsen KF.
cancer in men. J Natl Cancer Inst. 2001;93(17):1330-1336. https: Differential effects of casein versus whey on fasting plasma
//doi.org/10.1093/jnci/93.17.1330 levels of insulin, IGF-1 and IGF-1/IGFBP-3: results from a
55. King DG, Walker M, Campbell MD, Breen L, Stevenson EJ, randomized 7-day supplementation study in prepubertal
West DJ. A small dose of whey protein co-ingested with boys. Eur J Clin Nutr. 2009;63(9):1076-1083. https://doi.org/10.
mixed-macronutrient breakfast and lunch meals improves 1038/ejcn.2009.34
postprandial glycemia and suppresses appetite in men with 59. Burris J, Shikany JM, Rietkerk W, Woolf K. A low glycemic index
type 2 diabetes: a randomized controlled trial. Am J Clin and glycemic load diet decreases insulin-like growth factor-1
Nutr. 2018;107(4):550-557. https://doi.org/10.1093/ajcn/nqy among adults with moderate and severe acne: a short-
019 duration, 2-week randomized controlled trial. J Acad Nutr
56. Giezenaar C, Hutchison AT, Luscombe-Marsh ND, Chapman I, Diet. 2018;118(10):1874-1885. https://doi.org/10.1016/j.jand.
Horowitz M, Soenen S. Effect of age on blood glucose and 2018.02.009