Department of Orthopedic Surgery, Keio University School of Medicine, 35 Shinano-machi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Department of Orthopedic Surgery, Eiju General Hospital, 2-23-16 Higashiueno, Taito-ku, Tokyo, 110-8645, Japan.
Sci Rep. 2017 Mar 27;7(1):428. doi: 10.1038/s41598-017-00503-2.
Hip fracture is the most severe bone fragility fracture among osteoporotic injuries. Family history is a known risk factor for fracture and now included among criteria for osteoporosis diagnosis and treatment; however, genetic factors underlying family history favoring fracture remain to be elucidated. Here we demonstrate that a missense SNP in the ALDH2 gene, rs671 (ALDH2*2), is significantly associated with hip fracture (odds ratio = 2.48, 95% confidence interval: 1.20-5.10, p = 0.021). The rs671 SNP was also significantly associated with osteoporosis development (odds ratio = 2.04, 95% confidence interval: 1.07-3.88, p = 0.040). For analysis we enrolled 92 hip fracture patients plus 48 control subjects without bone fragility fractures with higher than -2.5 SD bone mineral density. We also recruited 156 osteoporosis patients diagnosed as below -2.5 SD in terms of bone mineral density but without hip fracture. Association of rs671 with hip fracture and osteoporosis was significant even after adjustment for age and body mass index. Our results provide new insight into the pathogenesis of hip fracture.
髋部骨折是骨质疏松性损伤中最严重的脆性骨折。家族史是骨折的已知危险因素,现在已被纳入骨质疏松症诊断和治疗标准;然而,导致家族史中骨折倾向的遗传因素仍有待阐明。在这里,我们证明 ALDH2 基因中的错义 SNP,rs671(ALDH2*2)与髋部骨折显著相关(优势比=2.48,95%置信区间:1.20-5.10,p=0.021)。rs671 SNP 也与骨质疏松症的发生显著相关(优势比=2.04,95%置信区间:1.07-3.88,p=0.040)。我们招募了 92 名髋部骨折患者和 48 名无脆性骨折但骨矿物质密度高于-2.5 SD 的对照受试者进行分析。我们还招募了 156 名骨质疏松症患者,这些患者的骨矿物质密度低于-2.5 SD,但没有髋部骨折。即使在调整年龄和体重指数后,rs671 与髋部骨折和骨质疏松症的相关性仍然显著。我们的研究结果为髋部骨折的发病机制提供了新的见解。