Nguyen Tuan V, Eisman John A
Healthy Ageing Theme Garvan Institute of Medical Research Sydney Australia.
St Vincent's Clinical School UNSW Medicine, UNSW Sydney Australia.
JBMR Plus. 2020 Sep 19;4(11):e10411. doi: 10.1002/jbm4.10411. eCollection 2020 Nov.
Over the past decade, through genome-wide association studies, more than 300 genetic variants have been identified to be associated with either BMD or fracture risk. These genetic variants are common in the general population, but they exert small to modest effects on BMD, suggesting that the utility of any single variant is limited. However, a combination of effect sizes from multiple variants in the form of the polygenic risk score (PRS) can provide a useful indicator of fracture risk beyond that obtained by conventional clinical risk factors. In this perspective, we review the progress of genetics of osteoporosis and approaches for creating PRSs, their uses, and caveats. Recent studies support the idea that the PRS, when integrated into existing fracture prediction models, can help clinicians and patients alike to better assess the fracture risk for an individual, and raise the possibility of precision risk assessment. © 2020 The Authors. published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
在过去十年中,通过全基因组关联研究,已鉴定出300多个与骨密度(BMD)或骨折风险相关的基因变异。这些基因变异在普通人群中很常见,但它们对骨密度的影响较小到中等,这表明任何单个变异的效用有限。然而,以多基因风险评分(PRS)形式的多个变异效应大小的组合,可以提供一个超出传统临床风险因素所获得的骨折风险有用指标。从这个角度出发,我们综述了骨质疏松症遗传学的进展、创建PRS的方法、其用途及注意事项。最近的研究支持这样一种观点,即当将PRS整合到现有的骨折预测模型中时,它可以帮助临床医生和患者更好地评估个体的骨折风险,并提高精准风险评估的可能性。© 2020作者。由Wiley Periodicals LLC代表美国骨与矿物质研究学会出版。