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ASPN D重复序列与骨关节炎关联的荟萃分析

Meta-analysis of association between the ASPN D-repeat and osteoarthritis.

作者信息

Nakamura Takahiro, Shi Dongquan, Tzetis Maria, Rodriguez-Lopez Julio, Miyamoto Yoshinari, Tsezou Aspasia, Gonzalez Antonio, Jiang Qing, Kamatani Naoyuki, Loughlin John, Ikegawa Shiro

机构信息

Laboratory for Statistical Analysis, SNP Research Center, RIKEN, Tokyo 108-8639, Japan.

出版信息

Hum Mol Genet. 2007 Jul 15;16(14):1676-81. doi: 10.1093/hmg/ddm115. Epub 2007 May 20.

Abstract

Osteoarthritis (OA) is the most common form of human arthritis. Genetic factors have been implicated in OA. It was reported that an aspartic acid (D)-repeat polymorphism in the gene encoding asporin (ASPN) was associated with OA of knee and hip joints in Japanese; in the three independent studies performed, the D14 allele of the ASPN polymorphism was over-represented and the D13 allele was under-represented. Subsequently, four replication studies, three in Europeans and one in Chinese populations, have been reported; however, they showed inconsistent results. To evaluate between-study heterogeneity and to estimate the common genetic effect of the D-repeat polymorphism on OA, we performed a meta-analysis of the five reports that include seven association studies, using the DerSimonian-Laird procedure. We detected association between knee OA and the susceptible D14 allele [P = 0.003, summary odds ratio (OR) = 1.46] with significant heterogeneity (P = 0.047) among the studies. We also detected positive association between knee OA and the protective D13 allele (P = 0.026, summary OR = 0.84) with significant heterogeneity (P = 0.040) among the studies. Because of significant heterogeneity, we stratified the studies by ethnicity. We detected positive association between knee OA and the D14 allele (P = 0.0000013, summary OR = 1.95) with non-significant heterogeneity (P = 0.535) in Asian populations. In hip OA, significant heterogeneity was identified and there was no positive association for any allele in any comparison. The present results suggest that the association of the ASPN D14 allele and knee OA has global relevance, but that its effect has ethnic differences.

摘要

骨关节炎(OA)是人类关节炎最常见的形式。遗传因素与骨关节炎有关。据报道,编码骨调素(ASPN)的基因中的天冬氨酸(D)重复多态性与日本人的膝关节和髋关节骨关节炎有关;在三项独立进行的研究中,ASPN多态性的D14等位基因过度表达,而D13等位基因表达不足。随后,有四项重复研究被报道,其中三项针对欧洲人群,一项针对中国人群;然而,这些研究结果并不一致。为了评估研究间的异质性,并估计D重复多态性对骨关节炎的共同遗传效应,我们使用DerSimonian-Laird方法对包含七项关联研究的五篇报告进行了荟萃分析。我们检测到膝关节骨关节炎与易感D14等位基因之间存在关联[P = 0.003,汇总比值比(OR)= 1.46],且研究间存在显著异质性(P = 0.047)。我们还检测到膝关节骨关节炎与保护性D13等位基因之间存在正相关(P = 0.026,汇总OR = 0.84),且研究间存在显著异质性(P = 0.040)。由于存在显著异质性,我们按种族对研究进行了分层。在亚洲人群中,我们检测到膝关节骨关节炎与D14等位基因之间存在正相关(P = 0.0000013,汇总OR = 1.95),异质性不显著(P = 0.535)。在髋关节骨关节炎中,发现存在显著异质性,在任何比较中任何等位基因均无正相关。目前的结果表明,ASPN D14等位基因与膝关节骨关节炎的关联具有全球相关性,但其效应存在种族差异。

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