| Literature DB >> 32929176 |
Gui-Juan Feng1,2, Xin-Tong Wei1,2, Hong Zhang2,3, Xiao-Lin Yang2,3, Hui Shen4, Qing Tian4, Hong-Wen Deng5, Lei Zhang6,7, Yu-Fang Pei8,9.
Abstract
Bone mineral density (BMD) and lean body mass (LBM) not only have a considerable heritability each, but also are genetically correlated. However, common genetic determinants shared by both traits are largely unknown. In the present study, we performed a bivariate genome-wide association study (GWAS) meta-analysis of hip BMD and trunk lean mass (TLM) in 11,335 subjects from 6 samples, and performed replication in estimated heel BMD and TLM in 215,234 UK Biobank (UKB) participants. We identified 2 loci that nearly attained the genome-wide significance (GWS, p < 5.0 × 10-8) level in the discovery GWAS meta-analysis and that were successfully replicated in the UKB sample: 11p15.2 (lead SNP rs12800228, discovery p = 2.88 × 10-7, replication p = 1.95 × 10-4) and 18q21.32 (rs489693, discovery p = 1.67 × 10-7, replication p = 1.17 × 10-3). The above 2 pleiotropic loci may play a pleiotropic role for hip BMD and TLM development. So our findings provide useful insights that further enhance our understanding of genetic interplay between BMD and LBM.Entities:
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Year: 2020 PMID: 32929176 PMCID: PMC7880826 DOI: 10.1038/s10038-020-00835-4
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172