首页> 美国卫生研究院文献>Comparative and Functional Genomics >A Pilot Genome-Wide Association Study in Postmenopausal Mexican-Mestizo Women Implicates the RMND1/CCDC170 Locus Is Associated with Bone Mineral Density
【2h】

A Pilot Genome-Wide Association Study in Postmenopausal Mexican-Mestizo Women Implicates the RMND1/CCDC170 Locus Is Associated with Bone Mineral Density

机译:绝经后墨西哥混血儿妇女的全基因组关联试验研究表明RMND1 / CCDC170基因座与骨矿物质密度有关

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

To identify genetic variants influencing bone mineral density (BMD) in the Mexican-Mestizo population, we performed a GWAS for femoral neck (FN) and lumbar spine (LS) in Mexican-Mestizo postmenopausal women. In the discovery sample, 300,000 SNPs were genotyped in a cohort of 411 postmenopausal women and seven SNPs were analyzed in the replication cohort (n = 420). The combined results of a meta-analysis from the discovery and replication samples identified two loci, RMND1 (rs6904364, P = 2.77 × 10−4) and CCDC170 (rs17081341, P = 1.62 × 10−5), associated with FN BMD. We also compared our results with those of the Genetic Factors for Osteoporosis (GEFOS) Consortium meta-analysis. The comparison revealed two loci previously reported in the GEFOS meta-analysis: SOX6 (rs7128738) and PKDCC (rs11887431) associated with FN and LS BMD, respectively, in our study population. Interestingly, rs17081341 rare in Caucasians (minor allele frequency < 0.03) was found in high frequency in our population, which suggests that this association could be specific to non-Caucasian populations. In conclusion, the first pilot Mexican GWA study of BMD confirmed previously identified loci and also demonstrated the importance of studying variability in diverse populations and/or specific populations.
机译:为了确定影响墨西哥Mestizo人群骨密度(BMD)的遗传变异,我们对墨西哥Mestizo绝经后妇女的股骨颈(FN)和腰椎(LS)进行了GWAS。在发现样本中,在411名绝经后妇女的队列中对300,000个SNP进行了基因分型,并在复制队列中对7个SNP进行了分析(n = 420)。来自发现和复制样本的荟萃分析的合并结果确定了两个基因座,RMND1(rs6904364,P = 2.77×10 -4 )和CCDC170(rs17081341,P = 1.62×10 -5 ),与FN BMD相关。我们还比较了我们的结果与骨质疏松症遗传因素(GEFOS)联盟荟萃分析的结果。这项比较揭示了先前在GEFOS荟萃分析中报告的两个基因座:我们的研究人群中分别与FN和LS BMD相关的SOX6(rs7128738)和PKDCC(rs11887431)。有趣的是,在我们的人群中以高频率发现了高加索人中稀有的rs17081341(次等位基因频率<0.03),这表明这种关联可能是特定于非高加索人群的。总之,墨西哥GWA对BMD的首次试点研究证实了先前确定的基因座,也证明了研究不同人群和/或特定人群变异性的重要性。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号