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A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass

  • Li Jun Tan
  • , Rong Liu
  • , Shu Feng Lei
  • , Rong Pan
  • , Tie Lin Yang
  • , Han Yan
  • , Yu Fang Pei
  • , Fang Yang
  • , Feng Zhang
  • , Feng Pan
  • , Yin Pin Zhang
  • , Hong Gang Hu
  • , Shawn Levy
  • , Hong Wen Deng
  • Hunan Normal University
  • University of Missouri at Kansas City
  • Xi'an Jiaotong University
  • Beijing Jiaotong University
  • Vanderbilt University

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Osteoporosis is a highly heritable common bone disease leading to fractures that severely impair the life quality of patients. Wrist fractures caused by osteoporosis are largely due to the scarcity of wrist bone mass. Here we report the results of a genome-wide association study (GWAS) of wrist bone mineral density (BMD). We examined ~500000 SNP markers in 1000 unrelated homogeneous Caucasian subjects and found a novel allelic association with wrist BMD at rs11023787 in the SOX6 (SRY (sex determining region Y)-box 6) gene (P=9.00×10-5). Subjects carrying the C allele of rs11023787 in SOX6 had significantly higher mean wrist BMD values than those with the T allele (0.485:0.462 g cm-2 for C allele vs. T allele carriers). For validation, we performed SOX6 association for BMD in an independent Chinese sample and found that SNP rs11023787 was significantly associated with wrist BMD in the Chinese sample (P=6.41×10-3). Meta-analyses of the GWAS scan and the replication studies yielded P-values of 5.20×10-6 for rs11023787. Results of this study, together with the functional relevance of SOX6 in cartilage formation, support the SOX6 gene as an important gene for BMD variation.

Original languageEnglish
Pages (from-to)1065-1072
Number of pages8
JournalScience China Life Sciences
Volume53
Issue number9
DOIs
StatePublished - Sep 2010

Keywords

  • GWAS
  • SNPs
  • SOX6
  • osteoporosis
  • wrist BMD

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