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Mandibular and Palatal Tori, Bone Mineral Density, and Salivary Cortisol in
Community-Dwelling Elderly Men and Women

Article  in  The Journals of Gerontology Series A Biological Sciences and Medical Sciences · December 2001
DOI: 10.1093/gerona/56.11.M731 · Source: PubMed

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Journal of Gerontology: MEDICAL SCIENCES Copyright 2001 by The Gerontological Society of America
2001, Vol. 56A, No. 11, M731–M735

Mandibular and Palatal Tori, Bone Mineral Density,


and Salivary Cortisol in Community-Dwelling Elderly
Men and Women
Jadwiga Hjertstedt,1 Edith A. Burns,2,3 Raymond Fleming,4 Hershel Raff,2,5 Inge Rudman,2,3
Edmund H. Duthie,2,3 and Charles R. Wilson6

1Division of Oral Medicine and Diagnostic Sciences, Marquette University School of Dentistry, Milwaukee, Wisconsin.
Departments of 2Medicine and 6Biophysics and Radiology, Medical College of Wisconsin, Milwaukee.
3Zablocki Veterans Affairs Medical Center, Milwaukee, Wisconsin.
4Department of Psychology, University of Wisconsin-Milwaukee.
5Endocrine Research Laboratory, St. Luke’s Medical Center, Milwaukee, Wisconsin.

Background. This investigation evaluated the relationship between the presence of tori and bone mineral density
(BMD) and salivary cortisol levels.

Methods. A total of 230 healthy, community-dwelling elderly men (n  129) and women (n  101) aged 60 and
older participated in this study. Forty-three women were on hormone replacement therapy (HRT). This was a compo-
nent of a 5-year longitudinal study measuring subjects’ body composition, hormone levels, physical activity, and diet
every 6 months. Subjects were examined for the presence of tori by visual inspection and digital palpation. BMD at six
sites was measured by dual-energy X-ray absorptiometry. Salivary cortisol levels were measured by radioimmunoassay.

Results. Twenty-three percent of all subjects had mandibular tori, 13% had palatal tori, and 12% had both mandibu-
lar and palatal tori. Mandibular tori were more common in men, and palatal tori were more common in women. The
presence of mandibular tori was significantly correlated with BMD of the lumbar spine, femoral neck, trochanter, and
Ward’s triangle for all subjects, and with the femoral neck and trochanter of women not on HRT. Men with palatal tori
had lower levels of salivary cortisol in the evening.

Conclusions. This study documented the high prevalence of mandibular and palatal tori in a group of 230 elderly,
community-dwelling subjects. Women not on HRT and all subjects taken as a group with mandibular tori had higher
BMD. The presence of tori at young adulthood may be a marker of higher BMD in the future and of a lower risk for de-
veloping osteoporosis.

M ANDIBULAR and palatal tori were first described


more than 100 years ago in the anthropological litera-
ture (1,2). They are considered to be relatively rare but nor-
with age. The onset of decline in bone mineral density
(BMD) in women occurs at an earlier age than in men, al-
though individual variations in the rate and degree of loss
mal anatomic formations. These benign bony hyperostoses are considerable (12). The peak BMD and rate of change of
are asymptomatic and begin to be clinically visible in the BMD vary at different skeletal sites depending on the ratio
second decade of life (3); they cease growing or exhibit of trabecular to cortical bone and on the average use at the
only minimal growth after the fourth decade (4). There are site (12). Numerous factors can affect BMD and the devel-
no longitudinal studies to suggest that they resorb over time. opment of osteoporosis, including extrinsic factors such as
Mandibular tori (MT), usually bilateral, are located on the nutrition, medication use, amount of physical activity, life-
lingual aspect of the mandible above the mylohyoid ridge style factors (e.g., smoking and alcohol abuse), and intrinsic
(5,6) (Figure 1). Palatal tori (PT) present symmetrically factors (e.g., adrenal and gonadal hormone levels). The rela-
along the mid-suture line of the hard palate. Tori consist of tionship between BMD and estrogen levels in women has
normal cancellous bone covered by a layer of cortical bone. been extensively studied, and an accelerated rate of BMD
They vary in size, can be flat or lobular, and can present as loss occurs during the immediate post-menopausal period
solitary nodules or multiple nodular masses that coalesce. (13). In men, a somewhat later and more gradual loss of
Their etiology is not fully understood, but hereditary and BMD has been associated with declining endogenous an-
functional or environmental factors, such as masticatory drogen levels (10,14,15). We (16) and others (17–22) have
stress, have been implicated in their manifestation (5,7). also recently reported an association between age and eleva-
Osteoporosis is a major health problem in the aging pop- tions in nadir cortisol levels. Our study also found a rela-
ulation, manifesting as structural bone changes, loss of bone tionship between higher nadir salivary cortisol and lower
mass, and increased incidence of fractures (8–11). Skeletal BMD in men and in women who have not used hormone re-
bone mass reaches its peak in the early thirties and declines placement therapy (HRT) (16).

M731
M732 HJERTSTEDT ET AL.

Veterans Affairs Medical Center. Subjects were recruited


from a group of community-dwelling men and women from
southeastern Wisconsin (60 years of age) participating in
a study of body composition changes with age that was
funded by the National Institute on Aging. Data on eco-
nomic status, years of education, smoking, and baseline di-
etary status have been described elsewhere (32). Excluded
from the study were those with symptomatic chronic dis-
ease of any organ system other than glaucoma, cataracts,
hypertension, treated idiopathic hypothyroidism, and de-
generative joint disease. Specific exclusionary criteria were
body weight 85% and 120% of ideal, recent weight
change of more than 5 pounds, presence of diabetes melli-
tus, a Folstein Mini-Mental State Examination score below
25, and the use of prescription medications other than anti-
histamines, non-narcotic analgesics, antihypertensives, and
Figure 1. Photograph of bilateral mandibular torus. The bony hy- thyroid or hormone replacement therapy. All subjects
perostoses are located on the lingual aspect of the mandible, poste- signed a separate consent form to participate in the dental
rior to the canines. Note the presence of a second hyperostosis poste- component of the study and were informed that not partici-
riorly on the left. pating in the dental/oral component would not influence
their participation in the ongoing project.

As with other bones in the skeleton, mandibular BMD de- BMD


creases with age (23–27). In a cross-sectional study of 85 os- Skeletal BMD was measured by dual-energy X-ray ab-
teoporotic women and 27 normal women, Kribbs and col- sorptiometry (DXA; Norland XR26, Fort Atkinson, WI) at
leagues (25,26) demonstrated decreased mandibular BMD six sites: the proximal and distal radius, the lumbar spine
and a thinner cortex at the gonion in osteoporotic women. (L2–4), the femoral neck, Ward’s triangle, and the intertro-
Another study reported greater cortical bone width and over- chanter region. Measurements were obtained every 6
all BMD of the mandible in men compared with women and months over a 5-year period.
declining BMD in both genders after age 50 (28). Autopsy
studies have found an inverse correlation between mandibu- Oral Examination
lar BMD and age, with lower values found in women com- All subjects were examined at the 4-year point of the 5-year
pared with men at all ages (29–31). Because tori appear to longitudinal study. A single investigator (J.H.), blinded to
stop growing at approximately the time that peak BMD is other data (e.g., hormone use and BMD), performed all
reached, we hypothesized that the two phenomena might be oral assessments, eliminating the risk of inter-examiner er-
interrelated. We are unaware of any studies evaluating the ror. Visual inspection and careful digital palpation deter-
relationship between tori and BMD. The purpose of this mined the presence or absence of MT and PT. No distinc-
study was to evaluate the relationship between the presence tion was made regarding the size or shape of tori. When
of tori and BMD and salivary cortisol levels in a group of applicable, subjects were asked to take out removable den-
community-dwelling elderly men and women. tures before the oral examination.

METHODS Salivary Cortisol Levels


Cortisol levels were measured in saliva obtained at 11 pm
Subjects (nadir in circadian rhythm) and 7 am (peak in circadian
The study was approved by the institutional review rhythm) at the 4-year point of the study. Subjects collected
boards of the Medical College of Wisconsin and Zablocki evening saliva at home and returned the samples for pro-

Table 1. Prevalence of Mandibular and Palatal Tori in 230 Elderly Subjects


HRT Women HRT Women All Women Men All Subjects
Group n (%) n (%) n (%) n (%) n (%)
Total sample 58 43 101 129 230
MT only 11 (19) 7 (16) 18 (18) 35 (27) 53 (23)
PT only* 12 (21) 8 (19) 20 (20) 9 (7) 29 (13)
Both 10 (17) 6 (14) 16 (16) 12 (9) 28 (12)
None 25 (43) 22 (51) 47 (47) 73 (57) 120 (52)

Notes: Numbers in parentheses in columns 2 through 5 represent the percentage of subjects in the gender group who did or did not have the indicated bone forma-
tion. Numbers in parentheses in the last column represent the percentage of all subjects with the indicated bone formation. HRT  not using hormone replacement
therapy; HRT  using hormone replacement therapy; MT  mandibular torus, PT  palatal torus.
*p  .05 comparing frequencies between men and women.
TORI AND BONE MINERAL DENSITY M733

Table 2. Mean Bone Mineral Density by Gender and Hormone Use than 10% were current smokers. The average length of time
at Year 4 (Phase 8) smoked was 22  2 years, and the average amount smoked
HRT Women HRT Women Men was 27  3 pack years.
Table 1 shows the prevalence of mandibular and palatal
BMD BMD BMD tori in this group of men and women. The presence of tori
Site (g/cm2) SD (g/cm2) SD (g/cm2) SD
was unrelated to age. The percentage of all subjects with
L2–4 0.904 0.021 1.018 0.025 1.174 0.019 only mandibular tori was 23% (53/230), the percentage with
Femoral neck 0.711 0.013 0.762 0.016 0.844 0.013 only palatal tori was 12.6% (29/230), and the percentage
Ward’s triangle 0.514 0.014 0.560 0.016 0.574 0.012
with both was 12.2% (28/230). MT only were present in
Trochanter 0.562 0.015 0.616 0.018 0.789 0.013
Proximal radius 0.238 0.006 0.277 0.007 0.371 0.006 27% of men and 18% of women (not significant). PT only
Distal radius 0.557 0.011 0.633 0.011 0.799 0.008 were significantly more common in women than in men
(20% vs 7%; 2  7.34, p  .01). The presence of tori in
Note: HRT  not using hormone replacement therapy; HRT  using
both locations occurred in 15.8% of women and 9.3% of
hormone replacement therapy; BMD  bone mineral density; SD  standard
deviation; L2–4  lumbar spine. men (not significant).
Mean BMD was greater in men than women and greater
in HRT women than in HRT women at all sites (Table
cessing on the same day they collected morning saliva. Sa- 2). This pattern was observed not only at the time of oral ex-
liva was sampled by having subjects chew on a cotton roll amination but throughout the study. Table 3 shows the cor-
(Salivette; Sarstedt, Newton, NC) for 2 to 3 minutes or until relations between BMD and the presence of mandibular
the cotton roll was soaked with saliva. Saliva was separated tori. For all subjects, the presence of mandibular tori was
from the cotton roll by centrifugation and then frozen. Sali- significantly correlated with BMD at the lumbar spine, fem-
vary cortisol concentration was measured by radioimmu- oral neck, trochanter, and Ward’s triangle. For HRT
noassay as previously described (33). The minimal detect- women, the presence of mandibular tori was directly and
able level was 0.4 nmol/l, and the interassay coefficient of significantly correlated with BMD at the femoral neck and
variation was 6% to 12%. trochanter site (Table 3). Because these subjects had been
involved in the longitudinal study for 4 years prior to oral
Data Analysis and Statistics examination, we wished to examine the relationship be-
Descriptive statistics, Pearson’s correlation coefficients, tween the presence of tori and BMD at baseline. For HRT
one-way analysis of variance (ANOVA), repeated measures women, the presence of mandibular tori correlated with
ANOVA, and categorical ANOVA were performed using Ex- BMD at the femoral neck 4 years earlier (r  .33, p  .02).
cel 7.0 (Microsoft, Redmond, WA) for personal computers and There were no significant correlations between the presence
SPSS for OSF/1, Release 6.1 (SPSS, Chicago, IL) software. A of tori and baseline BMD for HRT women or for men. No
p value of .05 was considered statistically significant. significant correlations were present between BMD of the
proximal and distal radius and mandibular tori in any group.
RESULTS Table 4 shows the correlations between BMD and the pres-
A total of 230 subjects agreed to participate in the oral/ ence of palatal tori. For all subjects combined, the presence
dental component. There were 129 men (aged 71  4 years, of a palatal torus was inversely related to BMD only at the
mean  SD) and 101 women (aged 70  4 years). At study proximal radius (r  .144, p  .041) and at the distal ra-
entry, 43 women were on hormone replacement therapy dius (r  .190, p  .007).
(HRT) and had been taking estrogen for at least 1 year,
and 58 women were not taking HRT (HRT). HRT were Salivary Cortisol, Tori, and BMD
somewhat younger than HRT (69  4 years vs 71  5 In men, there was a significant inverse correlation be-
years; p  .05). Slightly less than 30% of the 230 subjects tween evening salivary cortisol levels and the presence of a
gave a past history of smoking (n  68), although fewer palatal torus (r  0.21, p  .02). In other words, men with

Table 3. Correlations Between the Presence of Mandibular Tori and Bone Mineral Density at Year 4
HRT Women HRT Women Men All Subjects

(n  52) (n  39) (n  112) (n  203)

BMD Site r Value p Value r Value p Value r Value p Value r Value p Value
L2–4 .26 .06 .10 .89 .16 .07 .17 .02*
Femoral neck .31 .03* .11 .68 .15 .11 .16 .02*
Ward’s triangle .17 .23 .17 .29 .14 .13 .16 .02*
Trochanter .29 .04* .22 .39 .14 .15 .14 .05*
Proximal radius .17 .23 .15 .35 .09 .35 .13 .07
Distal radius .25 .08 .14 .40 .03 .76 .11 .12

Notes: BMD  bone mineral density; HRT  not using hormone replacement therapy; HRT  using hormone replacement therapy; L2–4 lumber spine.
Numbers represent Pearson’s correlation coefficients between BMD at the indicated site and presence of mandibular tori, with significant p values in bold text. Num-
ber of subjects is less than number of total subjects in study because not everyone had a dual-energy X-ray absorptiometry done at the time.
*p  .05
M734 HJERTSTEDT ET AL.

Table 4. Correlations Between the Presence of Palatal Tori and Bone Mineral Density at Year 4
HRT Women HRT Women Men All Subjects

(n  52) (n  39) (n  112) (n  203)

BMD Site r Value p Value r Value p Value r Value p Value r Value p Value
L2–4 .08 .58 .06 .73 .16 .08 .03 .68
Femoral neck .05 .72 .18 .29 .09 .35 .08 .24
Ward’s triangle .12 .40 .09 .58 .10 .31 .04 .60
Trochanter .09 .52 .30 .06 .17 .07 .13 .07
Proximal radius .08 .58 .18 .28 .11 .24 .14 .04*
Distal radius .03 .84 .24 .14 .05 .58 .19 .01*

Notes: BMD  bone mineral density; HRT  not using hormone replacement therapy; HRT  using hormone replacement therapy; L2–4 lumber spine.
Numbers represent Pearson’s correlation coefficients between BMD at the indicated site and presence of palatal tori, with significant p values in bold text. Number of
subjects is less than number of total subjects in study because not everyone had a dual-energy X-ray absorptiometry done at the time.
*p  .05

a palatal torus had significantly lower nadir cortisol levels scribe a significant relationship between mandibular tori
than men without a palatal torus. and BMD. Women who were not using HRT who also had
mandibular tori had significantly higher BMD at the femo-
DISCUSSION ral neck and trochanter. This suggests that the presence of
The primary purpose of this study was to investigate the mandibular tori early in life may be of prognostic value for
prevalence of tori and the relationship between mandibular the natural history of BMD loss in women after menopause.
and palatal tori, BMD, and adrenal and gonadal hormones The presence of tori in young adulthood may be a marker of
in a group of community-dwelling elderly subjects. In this higher peak BMD in the future and may possibly indicate a
group of initially healthy, predominantly Caucasian men lower risk for developing osteoporosis at more advanced
and women over the age of 65, more than 35% were found ages. The presence of palatal tori may also predict patterns
to have mandibular tori. The prevalence of tori in this popu- of cortisol dynamics with aging.
lation was at the high end of that reported in living popula-
tions by other investigators. In these studies, certain ethnic Acknowledgments
groups displayed high frequencies of tori (Eskimos and
This study was supported by NIH/NIA Grant AG 12010-10, the Veter-
Aleuts) compared with low frequencies in Caucasians, Afri- ans Affairs Research Service, GCRC Grant M01 RR00058-38, and St.
can Americans, and Asians (5,4,34,35,36). Higher frequen- Luke’s Medical Center.
cies have been reported in studies of skeletal remains, per- We thank Dr. Dale E. Mattson for help with the initial statistical analyses.
haps due to the mode of examination (5,37). Previous reports
Address correspondence to Dr. Jadwiga Hjertstedt, Division of Oral
also found a higher frequency of palatal tori compared with Medicine and Diagnostic Sciences, Marquette University School of Den-
mandibular tori (4,34). By contrast, the present study found tistry, P.O. Box 1881, Milwaukee, WI 53201-1881. E-mail: Jadwiga.
a higher frequency of mandibular tori with no difference be- Hjertstedt@marquette.edu
tween genders. Palatal tori were more common in women.
As expected, BMD was higher in men than women, and References
higher in HRT women than HRT women. There were 1. Danielli J. I perostosi in mandible umani specialmente di Ostiacchi ed
significant positive correlations between the presence of anche in mascellare superiore. Arch Anthropol Etnol. 1884;14:333–346.
mandibular tori and BMD for all subjects and for HRT 2. Fox J. The Natural History and Diseases of the Human Teeth. London:
women. There was a significant negative correlation be- Cox; 1814.
tween evening salivary cortisol and palatal tori in men. As 3. Axelsson G, Hedegaard B. Torus palatinus in Icelandic School chil-
dren. Am J Phys Anthropol. 1985;67:106–112.
we have recently described, men with higher salivary corti- 4. Kolas S, Halperin V, Jefferis K, et al. The occurrence of torus palati-
sol levels had lower BMD (16). The rate of bone loss was nus and mandibularis in 2,478 dental patients. Oral Surg Oral Med
similar for all subjects regardless of the presence or absence Oral Pathol. 1953;6:1134–1141.
of tori, gender, or use of HRT. The presence of tori appears 5. Hrdlika A. Mandibular and maxillary hyperostoses. Am J Phys An-
throp. 1940;27:1–55.
to be an indicator of denser skeletal mass in HRT women 6. Ossenberg NS. Mandibular torus: a synthesis of new and previously
and in the group as a whole. The subgroup of HRT reported data and a discussion of its cause. In: Cybulski JS, ed. Contri-
women had significantly greater BMD, and this relationship butions to Physical Anthropology, 1978–1980. Ottawa, Ontario,
appeared to override the significance of tori as an indicator Canada: National Museum of Canada; 1981:1–52.
of higher bone density. It should be emphasized that these 7. Eggen S, Natvig B. Torus mandibularis: an estimation of the degree of
genetic determination. Acta Odont Scand. 1989;47:409–415.
correlations, although statistically significant, were quite 8. Blumsohn A, Eastell R. Age-related factors. In: Riggs BL, Melton LJ,
low, as would be expected when many other factors are eds. Osteoporosis: Etiology, Diagnosis, and Management. 2nd ed.
likely to be stronger predictors of BMD. Philadelphia: Lippincott-Raven; 1995:161–182.
The underlying etiology of tori remains unclear, and it is 9. Krall EA, Dawson-Hughes B, Hirst K, Gallagher JC, Sherman SS,
Dalsky G. Bone mineral density and biochemical markers of bone
also uncertain if mandibular and palatal tori share the same turnover in healthy elderly men and women. J Gerontol Med Sci.
etiology. Little is known about the potential significance of 1997;52A:M61–M67.
tori for oral or general health. This is the first study to de- 10. Kenny AM, Gallagher JC, Prestwood KM, Gruman CA, Raisz LG.
TORI AND BONE MINERAL DENSITY M735

Bone density, bone turnover and hormone levels in men over age 75. J 24. Henrikson P-A, Wallenius K. The mandible and osteoporosis (1): a
Gerontol Med Sci. 1998;53A:M419–M425. quantitative comparison between the mandible and the radius. J Oral
11. Riggs BL, Wahner HW, Seeman E, et al. Changes in bone mineral Rehabil. 1974;1:67–74.
density of the proximal femur and spine with aging: differences be- 25. Kribbs PJ, Chestnut CH, Ott SM, Kilcoyne RF. Relationships between
tween the postmenopausal and senile osteoporosis syndromes. J Clin mandibular and skeletal bone in a population of normal women. J
Invest. 1982;70:716–723. Prosthet Dent. 1990;63:86–89.
12. Riggs BL, Melton LJ III. Involutional osteoporosis. N Engl J Med. 26. Kribbs PJ. Comparison of mandibular bone in normal and osteoporotic
1986;314:1676–1686. women. J Prosthet Dent. 1990;63:218–222.
13. Vico L, Prallet B, Chappard D, Pallot-Prades B, Pupier R, Alexandre 27. von Wowern N, Klausen B, Kollerup G. Osteoporosis: a risk factor in
C. Contributions of chronological age, age at menarche and meno- periodontal disease. J Periodontol. 1994;65:1134–1138.
pause and of anthropometric parameters to axial and peripheral bone 28. von Wowern N, Stoltze K. The pattern of age related bone loss in man-
densities. Osteoporos Int. 1992;2:153–158. dibles. Scand J Dent Res. 1980;88:134–146.
14. Jackson JA, Riggs MW, Spiekerman AM. Testosterone deficiency as a 29. Henrikson P-A, Wallenius K, Astrand K. The mandible and os-
risk factor for hip fracture in men: a case control study. Am J Med Sci. teoporosis (2). J Oral Rehabil. 1974;1:75–84.
1992;304:4–8. 30. Henrikson P-A, Wallenius K. The mandible and osteoporosis (1). J
15. Greendale GA, Edelstein S, Barrett-Connor E. Endogenous sex ste- Oral Rehabil. 1974;1:7–74.
roids and bone mineral density in older women and men: the Rancho 31. Dyer MRY, Ball J. Alveolar crest recession in the edentulous. Br Dent
Bernardo Study. J Bone Min Res. 1997;12:1833–1843. J. 1980;149:290–292.
16. Raff H, Raff JL, Duthie EH, et al. Elevated salivary cortisol in the 32. Abbasi A, Duthie EH, Sheldahl L, et al. Association of dehydroepi-
evening in healthy elderly men and women: correlation with bone androsterone sulfate, body composition, and physical fitness in
mineral density. J Gerontol Med Sci. 1999;54A:M479–M483. independent community dwelling old men and women. J Am Geriatr
17. Deuschle M, Gotthardt U, Schweiger U, et al. With aging in humans Soc. 1998;46:263–273.
the activity of the hypothalamus-pituitary-adrenal system increases 33. Raff H, Raff JL, Findling JW. Late-night salivary cortisol as a screen-
and its diurnal amplitude flattens. Life Sci. 1997;61:2239–2246. ing test for Cushing’s syndrome. J Clin Endocrinol Metab. 1998;83:
18. Van Cauter E, Leproult R, Kupfer DJ. Effects of gender and age on the 2681–2686.
levels and circadian rhythmicity of plasma cortisol. J Clin Endocrinol 34. Shah DS, Sanghavi SJ, Chawda JD, Shah RM. Prevalence of torus pa-
Metab. 1996;81:2468–2473. latinus and torus mandibularis in 1000 patients. Indian J Dent Res.
19. Copinschi G, Van Cauter E. Effects of aging on modulation of hor- 1992;3:107–110.
monal secretions by sleep and circadian rhythmicity. Horm Res. 1995; 35. Reichart PA, Neuhaus F, Sookasem M. Prevalence of torus palatinus
43:20–24. and torus mandibularis in Germans and Thai. Commun Dent Oral Epi-
20. Van Cauter E, Plat L, Leproult R, Copinschi G. Alterations of circa- demiol. 1988;16:61–64.
dian rhythmicity and sleep in aging: endocrine consequences. Horm 36. Nair RG, Samaranayake LP, Philipsen HP, Graham RG, Itthagarun A.
Res. 1998;49:147–152. Prevalence of oral lesions in a selected Vietnamese population. Int
21. Cugini P, Lucia P, Di Palma L, et al. The circadian rhythm of atrial Dent J. 1996;46:48–51.
natriuretic peptide, vasoactive intestinal peptide, beta-endorphin, and 37. Woo JK. Torus palatinus. Am J Phys Anthropol. 1950;8:81–109.
cortisol in healthy young and elderly subjects. Clin Autonom Res.
1992;2:113–118.
22. Nicolson N, Stroms C, Ponds R, Sulon J. Salivary cortisol levels and
stress reactivity in human aging. J Gerontol Med Sci. 1997;52A:M68–
M75. Received July 25, 2000
23. Atkinson PJ, Woodhead C. Changes in human mandibular structure Accepted December 5, 2000
with age. Arch Oral Biol. 1968;13:1453–1464. Decision Editor: John E. Morley, MB, BCh

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