Literature DB >> 29499414

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

Yu-Fang Pei1, Wen-Zhu Hu2, Min-Wei Yan3, Chang-Wei Li4, Lu Liu2, Xiao-Lin Yang2, Rong Hai5, Xiu-Yan Wang5, Hui Shen6, Qing Tian6, Hong-Wen Deng7, Lei Zhang8.   

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=5.0×10-8): 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.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  20p12.1; 20q13.33; Bone mineral density; Genome-wide association study; Osteoporosis

Mesh:

Year:  2018        PMID: 29499414      PMCID: PMC6329308          DOI: 10.1016/j.bone.2018.02.027

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


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