Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups by Xiong Dong-Hai, Liu Xiao-Gang, Guo Yan-Fang, Tan Li-Jun, Wang Liang, Sha Bao-Yong, Tang Zi-Hui, Pan Feng, Yang Tie-Lin, Chen Xiang-Ding, Lei Shu-Feng, Yerges Laura M, Zhu Xue-Zen, Wheeler Victor W, Patrick Alan L, Bunker ClareAnn H, Guo Yan, Yan Han, Pei Yu-Fang, Zhang Yin-Pin, Levy Shawn, Papasian Christopher J, Xiao Peng, Lundberg Y Wang, Recker Robert R, Liu Yao-Zhong, Liu Yong-Jun, Zmuda Joseph M, Deng Hong-Wen in American journal of human genetics (2009).

[PMID: 19249006] PubMed


To identify and validate genes associated with bone mineral density (BMD), which is a prominent osteoporosis risk factor, we tested 379,319 SNPs in 1000 unrelated white U.S. subjects for associations with BMD. For replication, we genotyped the most significant SNPs in 593 white U.S. families (1972 subjects), a Chinese hip fracture (HF) sample (350 cases, 350 controls), a Chinese BMD sample (2955 subjects), and a Tobago cohort of African ancestry (908 males). Publicly available Framingham genome-wide association study (GWAS) data (2953 whites) were also used for in silico replication. The GWAS detected two BMD candidate genes, ADAMTS18 (ADAM metallopeptidase with thrombospondin type 1 motif, 18) and TGFBR3 (transforming growth factor, beta receptor III). Replication studies verified the significant findings by GWAS. We also detected significant associations with hip fracture for ADAMTS18 SNPs in the Chinese HF sample. Meta-analyses supported the significant associations of ADAMTS18 and TGFBR3 with BMD (p values: 2.56 x 10(-5) to 2.13 x 10(-8); total sample size: n = 5925 to 9828). Electrophoretic mobility shift assay suggested that the minor allele of one significant ADAMTS18 SNP might promote binding of the TEL2 factor, which may repress ADAMTS18 expression. The data from NCBI GEO expression profiles also showed that ADAMTS18 and TGFBR3 genes were differentially expressed in subjects with normal skeletal fracture versus subjects with nonunion skeletal fracture. Overall, the evidence supports that ADAMTS18 and TGFBR3 might underlie BMD determination in the major human ethnic groups.

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