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Association Between rs11190870 Polymorphism Near LBX1 and Susceptibility to Adolescent Idiopathic Scoliosis in East Asian Population

机译:rs11190870多态性在LBX1附近与东亚人群青少年特发性脊柱侧凸的敏感性之间的关联

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Study Design. Meta-analysis to collect all the relevant studies to date to further investigate whether or not the rs11190870 polymorphism is associated with susceptibility to adolescent idiopathic scoliosis (AIS) in East Asian population. Objective. To investigate whether or not the rs11190870 polymorphism is associated with susceptibility to AIS in East Asian population.Summary of Background Data. To date, the single nucleotide polymorphism rs11190870 was identified as the most significant common variant in Japanese females. Three association studies conducted in Chinese Han population from Hong Kong, Yangtze River region, and Southern region of mainland China replicated the association between AIS and rs1190870. However, there is limited published data about the association of rs11190870 with AIS in East Asian population.Methods. A systematic search of all relevant studies published through August 2013 was conducted using the MEDLINE, EMBASE, OVID, and ScienceDirect. Single nucleotide polymorphism of rs11190870 was evaluated. The included studies were assessed in the analysis of the following allele model: T allele versus C allele for the allele-level comparison; (b) TC + TT versus CC for dominant model of T allele; (c) TT versus TC + CC for recessive model of T allele, and (d) TT versus CC for extreme genotype. Results. Four studies with 8415 total participants (2889 patients with AIS and 5526 controls), who were all East Asian population, were eligible for inclusion. We searched for genotypes T allele versus C allele, TT versus TC + CC, TC + TT versus CC, and TT versus CC in a fixed/random-effects model. The effect summary odds ratios and 95 % confidence intervals were obtained, which shows significant association between rs11190870 and AIS in East Asian populations (all genetic models P < 0.001). Subgroup analyses were conducted according to sex. The results showed a significant association between rs11190870 and AIS in female (all genetic models, P < 0.001) but not in male (all genetic models, P > 0.05). Conclusion. The present meta-analysis demonstrated that the T allele of single nucleotide polymorphism rs11190870 may be a major susceptibility locus in the East Asian population with AIS, especially in female.
机译:学习规划。荟萃分析收集了迄今为止的所有相关研究,以进一步调查rs11190870基因多态性是否与东亚人群青少年特发性脊柱侧凸(AIS)的易感性相关。目的。调查rs11190870基因多态性是否与东亚人群对AIS的易感性相关。背景数据摘要。迄今为止,单核苷酸多态性rs11190870被确定为日本女性中最重要的常见变异。在来自中国香港,长江和南部地区的汉族人群中进行的三项关联研究重复了AIS与rs1190870之间的关联。但是,关于rs11190870与AIS在东亚人群中的关联的公开数据很少。使用MEDLINE,EMBASE,OVID和ScienceDirect对截至2013年8月发表的所有相关研究进行了系统搜索。评估了rs11190870的单核苷酸多态性。在以下等位基因模型的分析中评估了纳入的研究:等位基因水平比较的T等位基因与C等位基因; (b)T等位基因优势模型的TC + TT与CC对比; (c)对于T等位基因的隐性模型,TT与TC + CC,以及(d)对于极端基因型,TT与CC + CC。结果。四项研究总共有8415名参与者(2889名AIS患者和5526名对照者),均为东亚人群,均符合纳入条件。我们在固定/随机效应模型中搜索了T等位基因对C等位基因,TT对TC + CC,TC + TT对CC和TT对CC的基因型。获得了效果汇总的优势比和95%的置信区间,这表明rs11190870与东亚人群的AIS之间存在显着关联(所有遗传模型P <0.001)。根据性别进行亚组分析。结果表明,rs11190870与AIS在女性(所有遗传模型,P <0.001)中有显着关联,而在男性(所有遗传模型,P> 0.05)中则没有。结论。目前的荟萃分析表明,单核苷酸多态性rs11190870的T等位基因可能是东亚人群AIS的主要易感基因位,尤其是女性。

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