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Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density

机译:两项全基因组关联荟萃分析的联合研究确定了20p12.1和20q13.33的骨矿物质密度

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摘要

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 × 10−8): 20p12.1 (rs73100693 p = 2.65 × 10−8, closest gene MACROD2) and 20q13.33 (rs2380128 p = 3.44 × 10−8, 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.
机译:在本研究中,为了确定与骨质疏松症相关的基因座,我们进行了两项独立的全基因组关联的股骨颈和腰椎骨矿物质密度(BMD)关联荟萃分析的联合关联研究:1)内部研究6个样本涉及7484个对象,2)GEFOS-seq研究对7个样本进行了32,965个对象。内部样本由1000个基因组计划第3阶段参考小组估算。在每个荟萃分析中,将基于SNP的关联测试应用于7,998,108个常染色体SNP,然后针对每个SNP将2个关联信号进行合并分析和相互复制。结合两项研究的证据,我们在全基因组显着性水平(α= 5.0×10 −8 )中确定了2个与BMD相关的新基因座:20p12.1(rs73100693 p = 2.65×10 < sup> -8 ,最接近的基因MACROD2)和20q13.33(rs2380128 p = 3.44×10 -8 ,OSBPL2)。我们还复制了两个有关脚跟和全身BMD的最新研究报告的7个基因座。我们的发现提供了有用的见解,可增进我们对骨骼发育,骨质疏松和骨折发病机理的了解。

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