Department of Epidemiology and Health Statistics, School of Public Health, Medical College of Soochow University, Jiangsu, PR China; Jiangsu Key Laboratory of Preventive and Translational Medicine for Geriatric Diseases, School of Public Health, Medical College of Soochow University, Jiangsu, PR China.
Jiangsu Key Laboratory of Preventive and Translational Medicine for Geriatric Diseases, School of Public Health, Medical College of Soochow University, Jiangsu, PR China; Center for Genetic Epidemiology and Genomics, School of Public Health, Medical College of Soochow University, Jiangsu, PR China.
Bone. 2018 May;110:378-385. doi: 10.1016/j.bone.2018.02.027. Epub 2018 Feb 28.
In the present study, aiming to identify loci associated with osteoporosis, we conducted a joint association study of 2 independent genome-wide association meta-analyses of femoral neck and lumbar spine bone mineral densities (BMDs): 1) an in-house study of 6 samples involving 7484 subjects, and 2) the GEFOS-seq study of 7 samples involving 32,965 subjects. The in-house samples were imputed by the 1000 genomes project phase 3 reference panel. SNP-based association test was applied to 7,998,108 autosomal SNPs in each meta-analysis, and for each SNP the 2 association signals were then combined for joint analysis and for mutual replication. Combining the evidence from both studies, we identified 2 novel loci associated with BMDs at the genome-wide significance level (α=5.0×10): 20p12.1 (rs73100693 p=2.65×10, closest gene MACROD2) and 20q13.33 (rs2380128 p=3.44×10, OSBPL2). We also replicated 7 loci that were reported by two recent studies on heel and total body BMD. Our findings provide useful insights that enhance our understanding of bone development, osteoporosis and fracture pathogenesis.
在本研究中,我们旨在鉴定与骨质疏松症相关的基因座,对股骨颈和腰椎骨密度(BMD)的 2 项独立全基因组关联荟萃分析进行了联合关联研究:1)一项包含 7484 名受试者的内部研究,以及 2)一项包含 32965 名受试者的 GEFOS-seq 研究。内部样本通过 1000 基因组项目第三阶段参考面板进行了单倍型分析。在每个荟萃分析中,对 7998108 个常染色体 SNP 进行了基于 SNP 的关联测试,对于每个 SNP,然后对 2 个关联信号进行了联合分析和相互复制。综合两项研究的证据,我们在全基因组显著水平(α=5.0×10)鉴定出 2 个与 BMD 相关的新基因座:20p12.1(rs73100693 p=2.65×10,最接近基因 MACROD2)和 20q13.33(rs2380128 p=3.44×10,OSBPL2)。我们还复制了最近两项关于足跟和全身 BMD 的研究报告的 7 个基因座。我们的发现提供了有用的见解,增强了我们对骨骼发育、骨质疏松症和骨折发病机制的理解。