GENETICS OF BONE DENSITY IN MEXICAN AMERICANS
GENETICS OF BONE DENSITY IN MEXICAN AMERICANS
批准号:
6375010
负责人:
BRAXTON D MITCHELL
金额:
$16.22万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-06-06 至 2002-05-31
关键词:
Mexican Americans biomarker body physical activity body physical characteristic bone density bone regeneration clinical research dietary calcium genetic markers genetics human genetic material tag human subject linkage mapping nutrition related tag osteocalcin osteogenesis osteoporosis pathologic bone resorption physiologic bone resorption vitamin D vitamin D receptors
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION: (Adapted from Investigator's Abstract) Osteoporosis is a
disabling condition characterized by loss of bone mass. There is strong
evidence that bone density is highly heritable, although the genes involved
are largely unknown. Recent studies have implicated the vitamin D receptor,
although the importance of this gene in modulating bone metabolism is
controversial. The overall goal of the proposed study is to identify and
characterize the genetic determinants of low bone density. The study
population will consist of 750 individuals, aged 20 yrs and older, who are
prior participants of the San Antonio Family Heart Study (SAFHS). During
the baseline examination of the SAFHS (1992-1996), extensive interviews were
obtained from all individuals on a wide range of medical and lifestyle
variables, including dietary habits and physical activity levels. Blood
samples were also drawn and DNA was collected for genetic analysis. In the
proposed study, these individuals will be re-examined, and bone density will
be measured at three sites by dual-photon absorptiometry (DEXA). Additional
biochemical markers of bone density-related phenotypes will also be
obtained. Eight candidate genes for osteoporosis will be genotyped,
including the vitamin D receptor locus. Under separate funding (as part of
the renewal for the SAFHS), funding has already been proposed to genotype a
panel of 391 microsatellite markers spanning the genome at approximately
10cM intervals.
Statistical genetic analyses will be performed to determine the effect of
the vitamin D receptor locus, and of the other candidate genes, on bone
density and related traits. Evidence for major genes will be detected
through segregation analysis. These genes will then be mapped to
chromosomal regions using the panel of microsatellite markers. Finally,
they will test whether the genetic effects on bone density are modified by
environmental factors. For example, they will determine if calcium intake
or physical activity is more strongly correlated with bone density in
individuals with the high risk vitamin D receptor genotype than in
individuals with the lower risk genotypes at this locus.
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