The Genetics of Bone Loss: Challenges and Prospects

被引:44
作者
Mitchell, Braxton D. [1 ]
Yerges-Armstrong, Laura M. [1 ]
机构
[1] Univ Maryland, Dept Med, Div Endocrinol Diabet & Nutr, Sch Med, Baltimore, MD 21201 USA
关键词
GENOME-WIDE ASSOCIATION; RECEPTOR-RELATED PROTEIN-5; DUBBO OSTEOPOROSIS EPIDEMIOLOGY; ANTONIO FAMILY OSTEOPOROSIS; CAG-REPEAT POLYMORPHISM; MINERAL DENSITY; POSTMENOPAUSAL WOMEN; FRACTURE RISK; FEMORAL-NECK; ELDERLY-MEN;
D O I
10.1210/jc.2010-2865
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Context: A strong genetic influence on bone mineral density has been long established, and modern genotyping technologies have generated a flurry of new discoveries about the genetic determinants of bone mineral density (BMD) measured at a single time point. However, much less is known about the genetics of age-related bone loss. Identifying bone loss-related genes may provide new routes for therapeutic intervention and osteoporosis prevention. Evidence Acquisition: A review of published peer-reviewed literature on the genetics of bone loss was performed. Relevant studies were summarized, most of which were drawn from the period 1990-2010. Evidence Synthesis: Although bone loss is a challenging phenotype, available evidence supports a substantial genetic contribution. Some of the genes identified from recent genome-wide association studies of cross-sectional BMD are attractive candidate genes for bone loss, most notably genes in the nuclear factor kappa B and estrogen endocrine pathways. New insights into the biology of skeletal development and regulation of bone turnover have inspired new hypotheses about genetic regulation of bone loss and may provide new directions for identifying genes associated with bone loss. Conclusions: Although recent genome-wide association and candidate gene studies have begun to identify genes that influence BMD, efforts to identify susceptibility genes specific for bone loss have proceeded more slowly. Nevertheless, clues are beginning to emerge on where to look, and as population studies accumulate, there is hope that important bone loss susceptibility genes will soon be identified. (J Clin Endocrinol Metab 96: 1258-1268, 2011)
引用
收藏
页码:1258 / 1268
页数:11
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