Sie sind auf Seite 1von 6

REMOVABLE PROSTHODONTICS

SECTION EDITORS
LOUIS BLATTERFEIN S. HOWARD PAYNE

Calcium metabolism and osteoporotic ridge


resorption: A protein connection
R. P. Blank, D.D.S.,* H. A. Diehl, Dr.HealthSc., M.P.H. (Nut&**
G. T. Ballard, D.M.D., M.S.,*** and R. C. Melendez, D.D.S., M.S.****
Naval Dental Clinic, Camp Pendleton, Calif., and Lifestyle Medicine Institute, Loma Linda, Calif.

lhe relationship of osteoporosis to alveolar and resid- Table I. Accumulative effect of long-term
ual ridge resportion is of justifiable concern to the dental negative calcium balance on osteoporosis-bone
profession. l-3 Although generalized bone loss is charac- loss
teristic of osteoporosis, the first sign may be alveolar
Total body calcium 1300 gm
bone loss, followed by loss in the vertebrae and long Skeletal calcium loss in 30 years if 540 gm
bones.‘T5It may be difficult to treat edentulous patients daily calcium balance is -50 mg
who manifest the excessive residual ridge resorption (50 mg X 365 days x 30 years)
often associated with osteoporosis. Kribbs et a1.3demon- Body calcium loss 42%
strated a significant correlation between skeletal osteope-
nia and the density of residual ridges and alveolar bone
but not with residual ridge reduction or periodontal costs of suffering, physical disability, and mortality
disease per se. They concluded that any therapeutic associated with the disease.*s9
measures that control or have an effect on osteoporosis Research in primary osteoporosis is currently focused
could therefore exert an effect on residual ridge density. on possible etiologic factors, such as diet, lifestyle,
A dentist, in a cooperative effort with a patient’s physical activity, and hormone status.8z‘Of” Although
physician, may be in a unique position to facilitate questions remain concerning the osteoporotic mechanism
prevention, early diagnosis, and treatment of this debili- and the exact nature of causative factors, it is clear that
tating disease.‘s6 osteoporosis is a result of excessive loss of bone calci-
This article reviews osteoporosis, discussesthe interre- um.
lationship between dietary protein, calcium metabolism,
and osteoporosis, and suggests a treatment regimen for CALCIUM METABOLISM
this condition. Although most of the body’s calcium is insoluble,
Osteoporosis may be defined simply as a condition of soluble calcium is maintained in a dynamic state by
insufficient bone. This deficiency undermines skeletal continuous absorption, exchange, deposition, resorption
strength, resulting in fractures that occur with minimal of bone, and excretion. ” Dietary absorption is the only
stress in the spine, distal radius and ulna, and in the means of obtaining calcium. There are nevertheless
femoral neck.5,7 Of the 190,000 hip fractures occurring several mechanisms whereby calcium is lost from the
annually, 80% are in postmenopausal women, attribut- body, including renal clearance, excretion of unabsorbed
ing to 40,000 deaths each year. It is estimated that 90% talcum in the feces, and dermal losses. If the amount of
of all fractures sustained in persons past the ages of 60 calcium absorbed is greater than the amount lost, excess
years are due to osteoporosis. The medical costs of calcium is deposited in the skeleton. This is referred to as
osteoporosis in the United States have been estimated at a positive calcium balance. Conversely, if losses exceed
almost $4 billion annually. That is in addition to the absorption, calcium is mobilized from the skeleton to
optimally maintain the narrow limits of extracellular
fluid calcium, and is thus termed negative calcium
The views expressed in this article are those of the authors and do not balance. A negative calcium balance sustained over an
reflect the official policy or position of the Department of the Navy,
Department of Defense, or the U.S. Government.
extended period of time will lead to osteoporosis (Table
*Lieutenant Commander, Dental Corps, United States Navy; Postdoc- I).’ Therefore, the primary goal of preventive and
toral Fellow in Prosthodontics. therapeutic regimens is to maintain a positive calcium
**Director, Lifestyle Medicine Institute. balance.
***Captain, Dental Corps, United States Navy; Head, Department of
Prosthodontics; Director, Postdoctoral Fellowship Program in TREATMENT MODALITIES
Prosthodontics.
****Captain, Dental Corps, United States Navy; Assistant Head, A complex array of etiologic factors in primary
Department of Prosthodontics. osteoporosis has been identified. Those factors include

590 NOVEMBER 1987 VOLUME 58 NUMBER 5


CALCIUM METABOLISM: A PROTEIN CONNECTION

decreased estrogen levels in postmenopausal women, Table II. Effect of low and high protein diets
inactivity, alcohol abuse, high phosphate diets, low on calcium balance
calcium diets, Vitamin D deficiency, corticosteroids,
Calcium balance
smoking, caffeine intake, dietary protein imbalance, and
stress.*,I3 Prevention and management of osteoporosis Calcium Low High
intake protein protein
include estrogen therapy, dietary Vitamin D, fluoride
Investigator (mg) (50 gm)’ (145 gm)*
supplementation, and increased calcium intake.
Estrogen therapy remains controversial because of Hegsted” 500 +24 -116
Anand and 500 +31 -120
uncertainty about long-term benefits.*,14Some authori-
Linkswile@
ties caution against routine use of estrogen in treating Walker and 800 +12 -85
osteoporosis because of associated risks, including uter- Linkswilef’*
ine cancer, thrombophlebitis, gall bladder disease,diabe- Linkswiler et aLso 1400 +20 -65
tes, and hypertension.‘, 15-‘* Johnson et a1.4’ 1400 +10 -84
Vitamin D is another widely used therapeutic adjunct Mean +19 -94
because of its important role in bone metabolism. The *+10?&
active metabolite of Vitamin D (1 alpha, 25-dihydroxy-
Vitamin D3) is actually a hormone synthesized by the
body through the action of sunlight on the skin. The tion between decreased bone density and low calcium
Vitamin D levels in a person’s body are a direct result of consumption in women over 45 years of age in the
the amount of sunlight received and are not dependent United States. Jowsey”, 3o and Lutwak3’ reported that
on dietary sources of the hormone.” Because of its calcium supplements were effective in reducing bone loss
questionable therapeutic role and potential toxicity, and showed that calcium/phosphorus ratios less than 1
some investigators conclude that Vitamin D supplemen- may lead to osteoporosis. These and other studies
tation should be approached with considerable cau- indicate protection against age-related bone loss in the
tion.932%z1 hand bones and alveolar and residual ridge bone with
Perhaps the most controversial experimental therapy increased calcium intake.1~31~32In contrast, several
for osteoporosis is the use of fluoride. Several groups studies reported no benefit to bone density from daily
have studied the effects of fluoride on the skeleton in calcium supplementation.22~“, 33,34
postmenopausal osteoporosis. A question to be answered This variance in reported data helps to explain the
is whether a fluoride-induced increase in bone mass will wide range in recommended dietary calcium intake from
also proportionally increase bone strength. Fluoridic various health organizations. The current recommended
bone displays increased crystallinity, which may actually dietary allowance (RDA) is 800 mg of calcium/day,
result in decreasedelasticity predisposing to fracture.*, 22 whereas the most recent National Institutes of Health
Although the fluoride therapy has been shown to (NIH) proposal calls for 1000 to 1500 mg of daily calci-
increase trabecular bone, studies to date suggest that it um.9B35 The World Health Organization (WHO) recom-
does not increase and may, indeed, decreasecortical bone mendation is only 400 to 500 mg of calcium/day inas-
density.9 Researchers suggest that one or more adverse much as calcium intake in most populations around the
side effects of fluoride therapy, including joint pains and world is 300 to 500 mg/day without any evidence of
gastric irritation, occur in 20% to 40% of treated osteoporosis.35,36That osteoporosis is epidemic in the
patients.*,9s23Fluoride therapy has not yet been approved United States, where consumption of dairy products and
by the Federal Drug Administration for treatment of calcium supplements is the highest in the world, is para-
osteoporosis and is considered an investigational doxical.9s37-39
Osteoporosis may not be simply a deficiency
drug.*, 9 disease, but a disease related to dietary excess.
Increasing calcium intake by means of dairy foods and
supplementation is the method most practiced in the THE PROTEIN CONNECTION
prevention and treatment of osteoporosis to optimize Nongeriatric American adults consume 105 to 120 gm
calcium balance. Reports on the relationship between of protein on average each day, far exceeding current
calcium intake and bone density are conflicting. Garn et RDA levels of 56 gm for men and 44 gm for women.35In
a1.,24Smith and Frame,25 and other researchers26*27 have addition to its association with kidney stones and pro-
failed to show a correlation between differences in gressive deterioration of renal function,40B4’ this excess
calcium intake and bone mass or rates of bone loss with protein may produce a calciuretic effect. As early as
age in adults. Matkovic et a1.28reported important 1920, Sherman42observed that adding meat to the diet
differences in bone mass in all ages between two caused an increase in urinary calcium excretion. The
ethnically similar Yugoslav groups who had calcium same observation was also noted between 1930 and 1952
intakes that differed by approximately a factor of two. in experiments in which meat or other high protein food
Similarly, Albanese et a1.29reported a statistical correla- was added to the diet.43-45

THE JOURNAL OF PROSTHETIC DENTISTRY 591


BLANK ET AL

150 - LOW PROTEIN INTAKE (47 dm)

s 100 -
posititie
.E

p 50.. l .

E 38 l -.... -.......,.......*i...............i...e
20 20
i 0
HIGH PROTEIN INTAKE (142 gm)
3
3 -50 - negative

i3

-100 - lc:r
?70

1 1. I I I k I I 1 1
500 800 1400
CALCIUM INTAKE (mg)

Fig, 1. Calciuti retention levels (mg) at different intakes of protein and calcium.
(Adapted from Linkswiler et al?‘)

Table III. Osteoporosis, dairy food, and Table IV. Calcium in selected foods
protein intake by countries9,37,38,39
Food Seiving mg
Dairy food Protein
Yoghurt, low fat 1 cup 415
Hip fractures intake intake
Greens,collard 1 cup 400
(rate/ (gmldayl (gxhldayl
Milk, low fat 1 cup 300
Country 100,000 :ivamen) person) person)
Greens,turnip 1 cup 250
United States 162 462 106 Chinesecabbage 1 cup 250
New Zealand 97 480 112 Greens,mustard tops 1 cu@ 200
Israel 70 315 105 Cottagecheese,low fat 1 cup 160
United Kingdom 63 455 90 Broccoli 1 cup 150
Hong Kong 31 95 82 Grains and pasta 1 cup 100-150
Singapore 15 113 82 Bread 2 slices 100
South African 5 10 55 Beans 1 cup 100
Bantu

In recent studies, only one group of investigators failed protein, despite daily calcium intake ad high as 1400 mg.
to demonstrate this calciuretic effect.46 Most studies The investigators concluded that the consumption of
consistently demonstrated a marked positive correlation high calcium diets is unlikely to prevent a negative
between the aniount of dietary protein intake and the calcidm balance and associated bone loss induced by the
level of calcium excretion (Table II).47-57Although not consumption of high protein diets.56
linear, varying protein intakes from less than 6 to 600
gm/day resulted in an increase of approximately 800% DISCUSSIdN
in urinary calcium excretion.52 Among the minei-als Observations of various world populations show a
studied (calcium, magnesium, sodium, potassium, and direct correlation between high protein intake and the
phosphorus) that relationship was unique for urinary incidence of ostedporosis (Table III).9a 37-39,
‘* Bantu tribes
calcium.52Studies have shown that men consuming diets living in Africa consume a daily average of 47 gm of
containing more than 95 gm of protein daily developed a predominately plant source protein and only 400 mg of
negative calcium balance even with high calcium intakes calcium. They are essentially free of osteoporosis. Even
(Fig. 1).4*,49In one long-term study, investigators mea- women who bear 5 to 10 children demonstrate that same
suring calcium in adults found a negative calcium finding.59-6’Genetic relatives of the Bantus in the United
balance even when subjects consumed only 75 gm of States consume a typically high protein diet and experi-

592 NOVEMBER 1987 VOLUME 58 NUMBER 5


CALCIUM METABOLISM: A PROTEIN CONNECTION

ence a rate of osteoporosis comparable with the rest of balanced diet is advocated by Wical and Swoope,’
the U.S. population. 62An example of the effects of excess Baxter,2 and others6b2’Recommendations relevant to the
protein is seen in the native Eskimos, who consume a prevention and management of osteoporosis are as
diet high in both protein (250 to 400 gm/day) and follows.
calcium (2000 mg/day). Despite high physical activity, 1. Avoid a high protein diet and maintain daily protein
the Eskimos have one of the highest rates of osteoporosis intake levels of 50 to 60 grams to promote a positive
in the world.63 calcium balance.
Atwood64 described the reduction of residual ridges as 2. Maintain the RDA of 800 mg of calcium for men and
a major oral disease entity dependent on several factors, nonpregnant women.
including anatomic, biologic, and mechanical factors. 3. Participate in regular exercise programs appropriate
Wical and Swoope’ suggested that this “oral disease” to age and health status.
type of resorption is a manifestation of osteoporosis. 4. Avoid risk factors related to osteoporosis such as
Baxter2 and Rowe6’ stated that when patients exhibit smoking, excessive alcohol, and the generous use of
rapid continuing bone resorption under well-fitting caffeine-containing beverages.
dental prostheses, osteoporotic bone loss must be consid- On a practical basis, this would include the following
ered as contributing to the etiology and pathogenesis of recommendations.
the disease process. This can lead to frustration for both Lower the consumption of animal products. This
dentist and patient as the otherwise inexplicable bone would not only decrease protein intake but would
loss progresses. Patients often return with complaints of have the added benefit of reducing cholesterol and fat
discomfort and inability to tolerate their prostheses.’ consumption.
Early loss of teeth and the need for more frequent reline Increase consumption of complex carbohydrate foods,
procedures for denture-wearing patients may also result. such as unrefined grains (rice, barley, breads, pasta,
Efforts to treat or prevent the dental manifestations of whole-grain cereals), potatoes, yams, squash, and
osteoporosis may concomitantly help the patient to avoid legumes (such as beans, peas, lentils).
the more grave effects of this disease. Increase consumption of vegetables, especially those
rich in calcium, such as broccoli, collard greens,
RECOMMENDATIONS turnips, kale, and Chinese cabbage (Table IV).
By the time osteoporosis is generally diagnosed, 50% Use moderate amounts of low fat or skim milk
to 75% of the original bone material has been lost from products as a source of calcium.
the skeleton.*,” For this reason alone, prevention
becomesimperative. Although the etiologic puzzle is still SUMMARY AND CONCLUSIONS
incomplete, the effect of protein on calcium metabolism The unique interrelationship between excess dietary
strongly suggests measurable benefits from a lifestyle protein, calcium metabolism, and osteoporosis with its
that avoids excessiveprotein in the diet. The adoption of associated ridge resorption has been reviewed. Recom-
a dietary lifestyle that reduces the protein intake to levels mendations for the prevention and management of
more in harmony with the RDA can dramatically osteoporosis have been discussed with concern for the
improve renal function40.4’ and serve as an effective calciuretic effect of a high protein diet customarily
means of restoring and maintaining a positive calcium consumed in American society. Positive calcium balance
balance. A positive calcium balance is necessary for promoted by the suggestedtreatment regimen may help
maximizing peak skeletal mass achieved during growth to preserve ridge integrity and at the same time prevent
and early adulthood and minimizing age-related bone the serious debilitating effects of generalized osteoporo-
loss that begins in the third or fourth decade of life.66 sis. Further research to evaluate for retardation and
Therapeutic and preventive measures, such as possible reversal of osteoporotic ridge resorption as
increasing calcium supplementation without regard for affected by dietary protein intake is warranted.
excessiveprotein intake, appear ineffectual in attaining a
positive calcium balance necessary in the prevention of We thank Commander A. W. Fehling, DC, U.S. Navy, for his
osteoporosis. The level of dietary protein must be helpful suggestions in editing this article prior to its submission for
considered when making recommendations for calcium publication.
requirements or allowances. For example, an individual
on a borderline high protein diet may not benefit from REFERENCES
recommendations of increasing the consumption of calci- 1. Wical KE, Swoope CC. Studies of residual ridge resorption. Part
um by eating more dairy products, as is the present II: The relationship of dietary calcium and phosphorus to
residual ridge resorption. J PROSTHET DENT 1974;32:13-22.
clinical custom, because dairy products are also high in 2. Baxter JC. Relationship of osteoporosis to excessive residual
protein. ridge resorption. J PROSTHET DENT 1981;46:123-5.
Educating patients about the importance of a properly 3. Kribbs PJ, Smith DE, Chestnutt CH III. Oral findings in

THE JOURNAL OF PROSTHETIC DENTISTRY 593


BLANK ET AL

osteoporosis. Part II: Relationship between residual ridge and EH. Problems of bone health in elderly. NY State J Med
alveolar bone resorption and generalized skeletal osteopenia. J 1975;75:326-36.
PROSTHET DENT 1983;50:719-24. 30. Jowsey J. Osteoporosis: dealing with a crippling bone disease of
4. Krook L, Lutwak L, Whalen JP, Henrikson PA, Lesser GV, the elderly. Geriatrics 1977;32:41-50.
Uris R. Human periodontal disease and osteoporosis. Cornell 31. Lutwak L. Dietary calcium and the reversal of bone demineral-
Vet 1972;62:371-91. ization. Nutr News 1974;37:1-4.
5. Lutak L. Continuing need for dietary calcium throughout life. 32. Albanese AA, Lorenz EJ, Wein EH. Osteoporosis: effects of
Geriatrics 1974;29:171-8. calcium. Am Fam Physician 1978;18: 160-7.
6. Bland JS. Calcium: where it should and shouldn’t be. Comple- 33. Shapiro J. Osteoporosis: evaluation of diagnosis and therapy.
mentary Med 1986;1:5-6. Arch Intern Med 1975;135:563-7.
7. Chestnut CH III. Treatment of postmenopausal osteoporosis: 34. Dud1 R. Evaluation of intravenous calcium therapy for osteopor-
some current concepts. Scott Med J 1981;26:72-80. osis. Am J Med 1973;55:631-7.
8. Lukert BP. Osteoporosis: a review and update. Arch Phys Med 35. National Research Council, Food and Nutrition Board, Commit-
Rehabil 1982;63:480-7. tee on Dietary Allowances. Recommended dietary allowances,
9. U.S. Department of Health and Human Services. National 9th rev ed. Washington DC: National Academy of Sciences,
Institutes of Health Consensus Development Conference State- 1980.
ment: program and abstracts: Osteoporosis. Bethesda, Md. 36. Heaney R. Calcium nutrition and bone health in the elderly. Am
National Institutes of Health, 1984. J Clin Nutr 1982;36:986-1013.
10. Jowsey J. Osteoporosis: its nature and the role of diet. Postgrad 37. Lewinnek G. The significance and comparative analysis of the
Med J 1976;60:75-9. epidemiology of hip fractures. Clin Ortho Related Res
11. Goodman CE. Osteoporosis: protective measures of nutrition and 1980;152:35-43.
exercise. Geriatrics 1985;40:59-70. 38. Food and Agriculture Organization (FAO) of the United
12. Chu J, Margen S. Dietary protein and calcium metabolism. Nations. Food Balance sheets: 1979-1981 Average. Rome, Food
Compr Ther 1979;5:62-7. and Agriculture Organization, 1984.
13. Albanese AA. Bone loss: causes, detection, and therapy. New 39. Food and Agriculture Organization of the United Nations.
York: Alan R Liss Inc, 1977. Production yearbook. 1984;37:263.
14. Riggs BL, Jowsey J, Ackerman E, Hazelrig JB. Short and long 40. Brenner B. Dietary protein and the progressive nature of kidney
term effects of estrogen in synthetic anabolic hormone in post- disease: the role of hemodynamically medicated glomerular
menopausal osteoporosis. J Clin Invest 1972;51:1659-63. injury in the pathogenesis of progressive glomerular sclerosis in
15. Judd H. Estrogen replacement therapy: indications and compli- aging, renal oblation, and intrinsic renal disease. N Engl J Med
cations. Ann Intern Med 1983;98:195-205. 1982;307:652-9.
16. Boston Collaborative Drug Surveillance Program. Surgically 41. Walser M. Nutritional support in renal failure: future directions.
confirmed gallbladder disease, venous thromboembolism, and Lancet 1983;1:340-2.
breast tumors in relation to postmenopausal estrogen therapy. N 42. Sherman HC. Calcium requirements in man. J Biol Chem
Engl J Med 1974;290:15-9. 1920;44:21-7.
17. Atabor L. Effect of exogenous estrogen on carbohydrate metabo- 43. McClellan WS, DuBois EF. Clinical calorimetry: prolonged
lism in postmenopausal women. Am J Obstet Gynecol 1972; meat diets with a study of the metabolism of nitrogen, calcium,
113:383-7. and phosphorous. J Biol Chem 1930;87:669-80.
18. Pfeffer R. Estrogen use and stroke risk in postmenopausal 44. Pittman MS, Kunerth BL. A long time study of nitrogen,
women. Am J Epidemiol 1976;103:445-56. calcium, and phosphorous metabolism on a medium protein diet.
19. Fraser D. The physiological economy of Vitamin D. Lancet J Nutr 1939;17:175-85.
1983;1:969-71. 45. Hegsted DM, Moscoso I, Collazos C. A study of the minimum
20. Nizel AE. Nutrition in preventive dentistry: science and practice. calcium requirements of adult men. J Nutr 1952;46:181-201.
2nd ed. Philadelphia: WB Saunders Co, 1981. 46. Spencer H, Kramer L, DeBartolo M, et al. Further studies of the
21. Deluca H. The latest information on Vitamin D and bone status. effect of a high protein diet as meat on calcium metabolism. Am J
Complementary Med 1986;1:13-6. Clin Nutr 1983;37:924-9.
22. Christiansen C. Prevention of early postmenopausal bone loss: 47. Johnson NE, Alcontara EN, Linkswiler H. Effect of level of
controlled 2-year study in 315 normal females. Eur J Clin Invest protein intake on urinary and fecal calcium retention in young
1980;10:273-9. adult males. J Nutr 1970;100:1425-30.
23. Riggs B. Effect of the fluoride/calcium regimen on vertebral 48. Walker RM, Linkswiler HM. Calcium retention in the adult
fracture occurrence in postmenopausal osteoporosis: comparison human male as affected by protein intake. J Nutr 1972;
with conventional therapy. N Engl J Med 1982;306:446-50. 102:1297-1302.
24. Garn SM, Rohmann CG, Wagner B, Ascoli W. Continuing bone 49. Anand DR, Linkswiler HM. Effect of protein intake on calcium
growth throughout life: general phenomenon. Am J Phys balance of young men given 500 mg calcium daily. J Nutr
Anthropol 1967;26:313-7. 1974;104:695-700.
25. Smith RW Jr, Frame B. Concurrent axial and appendicular 50. Linkswiler HM, Joyce CL, Anand CR. Calcium retention of
osteoporosis: its relation to calcium consumption. N Engl J Med young adult males as affected by level of protein and of calcium
1965;273:73-8. intake. Trans NY Acad Sci 1974;36:330-40.
26. Hegsted DM. Mineral intake and bone loss. Fed Proc 51. Schwartz R, Woodcock NA, Blakely JD, Mackellar I. Metabolic
1967~26~1747-54. response of adolescent boys to two levels of dietary magnesium
27. Nilas L. Calcium supplementation and postmenopausal bone and protein. II. Effect of magnesium and protein level on calcium
loss. Br Med J 1984;289:1103-6. balance. Am J Clin Nutr 1973;26:519-23.
28. Matkovic V, Kostial K, Simovovic I, et al. Bone status and 52. Margen S, Chu JY, Kaufmann NA, Galloway DH. Studies in
fracture rates in two regions of Yugoslavia. Am J Clin Nutr calcium metabolism. I. The calciuretic effect of dietary protein.
1979;32:540-9. Am J Clin Nutr 1974;27:584-9.
29. Albanese AA, Edelson AH, Lorenae EJ, Woodhall ML, Wein 53. Chu JY, Margen S, Costa FM. Studies in calcium metabolism.

594 NOVEMBER 1957 VOLUME 55 NUMBER 5


CALCIUM METABOLISM: A PROTEIN CONNECTION

II. Effects of low calcium intake and variable protein intake on 61. Solomon L. Osteoporosis and fracture of the femoral neck in the
human calcium metabolism. Am J Clin Nutr 1975;28:1028-35. South African Bantu. J Bone Joint Surg 1968;50B:2-13.
54. Chu JY, Costa FM, Margen S. Effects of low calcium and 62. Smith R. Epidemiologic studies of osteoporosis in women in
variable protein intake on human radio-calcium kinetics. Nutr Puerto Rico and southeastern Michigan with special reference to
Rept Intern 1978;17:503-8. age, race, national origin, and to other related or associated
55. Allen LH, Bartlett RS, Block GD. Reduction of renal calcium findings. Clin Orthop 1966;45:31-48.
reabsorption in man by consumption of dietary protein. J Nutr 63. Mazess R. Bone mineral content of North Alaskan Eskimos. Am
1979;109:1345-50. J Clin Nutr 1974;27:916-25.
56. Allen LH, Oddoye EA, Margen S. Protein-induced hypercalciu- 64. Atwood DA. Reduction of residual ridges: a major oral disease
ria: a longer term study. Am J Clin Nutr 1979;32:741-9. entity. J PROSTHET DENT 1971;26:266-79.
57. Hegsted DM. Urinary calcium and calcium balance in young 65. Rowe DJ. Bone loss in the elderly. J PROSTHET DENT
men as affected by level of protein and phosphorous intake. J 1983;50:607-10.
Nutr 1981;111:553-62. 66. Consensus Conference. Osteoporosis. JAMA 1984;252:799-
58. Chalmers J. Geographical variations in senile osteoporosis. J 802.
Bone Joint Surg 1970;52B:667-75.
Reprint requests to:
59. Walker AR. Osteoporosis and calcium deficiency. Am J Clin
LCDR R. P. BLANK, DC, USN
Nutr 1965;16.327-36.
NAVAL DENTAL CLINIC
60. Walker AR. The influence of numerous pregnancies and lacta-
PLJCET SOUND NAVAL SHIPYARD
tions on bone dimensions in South African Bantu and Caucasian
BREMERTON, WA 98314
mothers. Clin Sci 1972;42:189-96.

Objective testing of the efficiency of


denture-cleansing agents
Shogo Minagi, D.D.S., Ph.D.,* Tatsuhiko Tsunoda, D.D.S.,**
Koichiro Yoshida, D.D.S., Ph.D.,* and Hiromichi Tsuru, D.D.S., Ph.D.***
Hiroshima University, School of Dentistry, Hiroshima, Japan

li aque on the tissue surface of a denture is an


important factor in the pathogenesis of denture stomati-
tis and many studies have been conducted to evaluate the
efficacy of denture-cleansing methods.lW7Nevertheless,
variations in denture plaque have made it difficult to
evaluate the clinical efficacy of the many available
denture-cleansing agents. This study reports a method of
objective evaluation of denture-cleansing agents.
UPPER (25 areas 1 LOWER (15 areas)
MATERIAL AND METHODS
Fig. 1. Area segmentation for upper and lower den-
Two upper and one lower complete dentures worn for tures.
more than 2 years by patients (three donors, A, B, and
C) 58 to 71 years of age were used in the study. After
new dentures were made for the patients, each old upper denture and 15 zones for the lower denture (Fig.
denture was cut into test pieces in the following man- 1). Each zone was further cut into four test pieces
ner. approximately 5 X 5 mm. The four test pieces from each
The test dentures were divided into 25 zones for the zone were randomly distributed to four groups consisting
of a control group and three cleansing-agent groups
according to the statistical method of randomized block
*Instructor, Department of Removable Prosthodontics.
**Research Fellow, Department of Removable Prosthodontics. design. This format resulted in each group having either
***Professor and Chairman, Department of Removable Prosthodon- 25 upper-denture or 15 lower-denture test pieces of
tics. 5 X 5 mm. Three immersion denture-cleansing agents

THE JOURNAL OF PROSTHETIC DENTISTRY 595

Das könnte Ihnen auch gefallen