Department of Medicine, Division of Endocrinology, Diabetes, and Nutrition, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
J Clin Endocrinol Metab. 2011 May;96(5):1258-68. doi: 10.1210/jc.2010-2865. Epub 2011 Feb 23.
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.
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.
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 κB 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.
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.
骨骼密度受遗传因素的影响很大,现代基因分型技术在单个时间点测量的骨骼密度(BMD)的遗传决定因素方面产生了大量新发现。然而,关于与年龄相关的骨质流失的遗传学知识却知之甚少。确定与骨质流失相关的基因可能为治疗干预和骨质疏松症预防提供新途径。
对骨骼流失遗传学的已发表同行评议文献进行了综述。总结了相关研究,其中大多数研究来自 1990 年至 2010 年期间。
尽管骨质流失是一种具有挑战性的表型,但现有证据表明其具有很大的遗传贡献。从横断面 BMD 的全基因组关联研究中鉴定出的一些基因是骨质流失的有吸引力的候选基因,尤其是核因子κB 和雌激素内分泌途径中的基因。骨骼发育和骨转换调控生物学的新见解激发了关于遗传调控骨质流失的新假设,并可能为鉴定与骨质流失相关的基因提供新方向。
尽管最近的全基因组关联和候选基因研究已经开始鉴定影响 BMD 的基因,但识别专门针对骨质流失的易感基因的努力进展较为缓慢。尽管如此,有关从何处入手的线索开始浮现,随着人群研究的积累,有望很快确定重要的骨质流失易感基因。