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Phytoestrogens May Play a Role in Prevention and Treatment of Osteoporosis in Postmenopausal Women

By Caroline Kanzaiza

 

O

varian hormone deficiency is a major risk factor for osteoporosis in postmenopausal women. Hormone replacement therapy (HRT) is one of the treatments used to alleviate postmenopausal symptoms; to lower the risk for coronary heart disease and perhaps it could be the most effective treatment for osteoporosis, since it has been demonstrated to both reduce the rate of bone loss and risk of fracture. However, more than 80% of postmenopausal women do not consent to hormone replacement therapy, either because of fear of increased risk of certain types of cancer or contraindications. As a result, postmenopausal women are more inclined to use natural remedies to alleviate these symptoms and help reduce their risk for chronic diseases such as osteoporosis. Recent reports show that certain bioactive constituents, such as phytoestrogens, which are non-steroidal plant compounds naturally found in fruits, vegetables, and grains play a role in maintaining or improving bone health. Phytoestrogens act like selective estrogen receptor modulators in tissues. Hence dietary intake of food sources high in phytoestrogens such as soybeans, flaxseed, and certain types of fruits and vegetables high in polyphenolic compounds may provide a practical and safe alternative treatment in postmenopausal women.

Several animal and human studies have been conducted to assess the role of soy or its isoflavones on bone health. For example, a six-month study conducted to examine the lipid-lowering properties of soy protein in postmenopausal women showed that isoflavone-rich soy protein increased lumbar spine bone mineral density (BMD) and bone mineral content (BMC). Another study of similar duration indicated that the percentage change in lumbar spine bone mineral density (BMD) or bone mineral content (BMC) in perimenopausal women did not decline from baseline in the isoflavone-rich soy group, but significantly declined in the control group that received isoflavone-poor supplement.

Results from a trial conducted to evaluate the effects of soy protein isolates with three levels of isoflavones on markers of bone turnover in 14 premenopausal and 17 postmenopausal women, concluded that, effects of soy isoflavones on markers of bone turnover were of small magnitude and unlikely to be clinically relevant. However, another study involving 50 postmenopausal women who received 60–70 mg of isoflavones in the form of soymilk for 12 weeks demonstrated reduction in the rate of bone resorption and enhanced the rate of bone formation. This is supported by unpublished data obtained from a trial, involving consumption of 40 g soy protein delivering 90 mg isoflavones daily for a period of three months which significantly indicated reduced urinary deoxypyridinoline (Dpd) excretion and elevated serum insulin-like growth factor I (IGF-I) concentrations in women under or above age 65 regardless of their estrogen status. The above results show inconsistencies that could be attributed to numerous confounding factors such as age, menopausal status and isoflavone content of the soy regimens provided.


 

Another important plant is flaxseed, which is rich in lignans, a type of phytoestrogens. Lignans are believed to have antioxidant properties and to reduce the rate of bone loss. Flaxseed is also rich in alpha-linolenic acid that reduces the rate of bone resorption by inhibiting biosynthesis of prostaglandins.

Dried plums or prunes and other food sources of phenolic compounds and flavonoids may also prevent bone loss. This is because these phytochemicals have antioxidant properties and can protect the bone by scavenging free radicals. Dried plums are also rich sources of selenium and boron minerals, which modulate bone metabolism and preserve bone mineral density. Unpublished findings from a study carried out to asses the effect of plum supplementation in postmenopausal women not on hormone replacement therapy (HRT), indicated that dried plums have the ability to increase bone formation in postmenopausal women and decreases the risk for osteoporotic fractures.

In conclusion soy has a modest effect on bone health. However, it is still premature to state whether it is soy protein or its isoflavones that prevent bone loss in ovarian hormone deficiency. Researchers are findings this as an important basis for further research on establishing the role of soy in health bones and its efficacy as a safe alternative treatment and prevention for bone loss in postmenopausal women, since soy is cheap and can easily be incorporated into the daily diet or provided as a concentrate for supplementation.

 


References

Alekel DL, St Germain A, Peterson C, Hanson K, Stewart JW, Toda T: Isoflavone-rich soy protein isolate attenuates bone loss in the lumbar spine of perimenopausal women . Am J Clin Nutr 72:844–852, 2000.

Bahram H. Arjmandi: The Role of Phytoestrogens in the Prevention and Treatment of Osteoporosis in Ovarian Hormone Deficiency . Journal of the American College of Nutrition, Vol. 20, No. 5, 398S–402S (2001)

Bonnic SL: AMWA position statement on osteoporosis. J Am Med Women Assoc 45:75–79, 1990.

Brzezinski A, Debi A: Phytoestrogens: the “natural” selective estrogen receptor modulators. Eu J Obstet Gynecol Rep Biol 85:47–51, 1999.

Cosman F, Lindsay R : Selective estrogen receptor modulators: Clinical spectrum. Endocr Rev 20:418–434, 1999.

Dempster DW, Lindsay R: Pathogenesis of osteoporosis. Lancet 341:797–801, 1996.

Johannes CB, Crawford SL, Posner JG, McKinlay SM: Longitudinal patterns and correlates of hormone replacement therapy use in middle-aged women . Am J Epidemiol 140:439–452, 1994.

Mundy GR: Visions for the future in osteoporosis research. Osteoporos Int 2(Suppl): 29S–34S, 1993.

Tolstoi LG, Levin RM: Osteoporosis—the treatment controversy. Nutr Today 27:6–12, 1992.

Wangen KE, Duncan AM, Merz-Demlow BE, Xu X, Marcus R, Phipps WR, Kurzer MS: Effects of soy isoflavones on markers of bone turnover in premenopausal and  postmenopausal women . J Clin Endocrinol Metab 85:3043–3048, 2000.

Last Updated on Wednesday, 10 October 2007
 
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