Genetic factors in osteoporosis. What are the implications for prevention and treatment?

Abstract:

:Osteoporosis is a common disease that affects 1 in 3 women. Family and twin studies have demonstrated that there is a strong genetic component to this condition. Potential candidate genes examined for their regulatory effect on bone mass include those for collagen type I, estrogen and vitamin D receptors, and various cytokines and growth factors. To date, most work has focused on the vitamin D receptor (VDR) gene, and experience with this locus will probably act as a model for many future studies. There is increasing evidence, from population studies that have examined the relationship between VDR genotype and bone mineral density, of genetic heterogeneity and gene-environment interactions. Response to therapeutic agents may also be affected by an individual's underlying genotype, partly explaining the range of responses that are commonly observed in clinical practice. Knowledge of a person's genotype could, therefore, allow current therapies to be targeted to those most likely to benefit, with a possible reduction in adverse effects. Largescale genomic studies of osteoporosis may also identify novel genes, and this may lead to both a better understanding of disease pathophysiology and to the discovery of potential targets for drug development.

journal_name

Drugs Aging

journal_title

Drugs & aging

authors

Keen RW,Kelly PJ

doi

10.2165/00002512-199711050-00001

subject

Has Abstract

pub_date

1997-11-01 00:00:00

pages

333-7

issue

5

eissn

1170-229X

issn

1179-1969

journal_volume

11

pub_type

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