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Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.全生命周期全基因组关联研究荟萃分析与骨密度的关联,以及对年龄特异性效应的评估。
Am J Hum Genet. 2018 Jan 4;102(1):88-102. doi: 10.1016/j.ajhg.2017.12.005.
2
Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.鉴定出153个与跟骨骨密度相关的新基因座以及GPC6在骨质疏松症中的功能作用。
Nat Genet. 2017 Oct;49(10):1468-1475. doi: 10.1038/ng.3949. Epub 2017 Sep 4.
3
Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation.全基因组关联研究荟萃分析用于骨定量超声参数,确定了五个与宽带超声衰减相关的新基因座。
Hum Mol Genet. 2017 Jul 15;26(14):2791-2802. doi: 10.1093/hmg/ddx174.
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Meta analysis identifies a novel susceptibility locus associated with heel bone strength in the Korean population.荟萃分析确定了一个与韩国人群足跟骨强度相关的新的易感基因座。
Bone. 2016 Mar;84:47-51. doi: 10.1016/j.bone.2015.12.005. Epub 2015 Dec 12.
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Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.全基因组测序确定EN1是骨密度和骨折的一个决定因素。
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Identification of a novel FGFRL1 MicroRNA target site polymorphism for bone mineral density in meta-analyses of genome-wide association studies.在全基因组关联研究的荟萃分析中鉴定一种新的FGFRL1微小RNA靶位点多态性与骨密度的关系
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STRING v10: protein-protein interaction networks, integrated over the tree of life.STRING v10:整合了整个生命之树的蛋白质-蛋白质相互作用网络。
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FISH: fast and accurate diploid genotype imputation via segmental hidden Markov model.FISH:通过分段隐马尔可夫模型实现快速准确的二倍体基因型填充
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两项全基因组关联荟萃分析的联合研究鉴定出了骨密度的 20p12.1 和 20q13.33 两个位点。

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

机构信息

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.

出版信息

Bone. 2018 May;110:378-385. doi: 10.1016/j.bone.2018.02.027. Epub 2018 Feb 28.

DOI:10.1016/j.bone.2018.02.027
PMID:29499414
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6329308/
Abstract

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.

摘要

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。