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PTGDR 多态性与哮喘易感性的关系:一项荟萃分析。

PTGDR polymorphisms and susceptibility to asthma: a meta-analysis.

机构信息

Division of Rheumatology, Department of Internal Medicine, Korea University Anam Hospital, Korea University College of Medicine, 126-1, Anam-dong 5-ga, Seongbuk-gu, Seoul, 136-705, South Korea.

出版信息

Mol Biol Rep. 2013 Mar;40(3):2195-203. doi: 10.1007/s11033-012-2280-x. Epub 2012 Nov 29.

Abstract

The aim of this study was to explore whether prostaglandin D2 receptor (PTGDR) polymorphisms confer susceptibility to asthma. A meta-analysis was conducted on the associations between the PTGDR -549 C/T, -441 C/T, and -197 C/T polymorphisms and asthma using: (1) allele contrast, (2) the recessive model, (3) the dominant model, and (4) the additive model. Three polymorphism haplotypes were constructed in the order -549/-441/-179. Meta-analysis was performed on the haplotype CCC (high transcriptional activity) and of TCT (low transcriptional activity). A total of 13 separate comparative studies in 9 articles involving 7,155 patients with asthma and 7,285 control subjects were included in this meta-analysis. An association between asthma and the PTGDR -549 C/T polymorphism was found by allele contrast (OR = 1.133, 95 % CI = 1.004-1.279, P = 0.043). Ethnicity-specific meta-analysis showed an association between asthma and the PTGDR -549 C allele in Europeans (OR = 1.192, 95 % CI = 1.032-1.377, P = 0.017). Furthermore, stratifying subjects by age indicated an association between the PTGDR -549 C allele and asthma in adults (OR = 1.248, 95 % CI = 1.076-1.447, P = 0.003), but no association in children (OR = 0.933, 95 % CI = 0.756-1.154, P = 0.324). Analyses using the dominant and additive models showed the similar pattern as that observed for the PTGDR -549 C allele, that is, a significant association in Europeans and adults, but not in children. No association was found between asthma and the PTGDR -441 C/T or -197 C/T polymorphisms, and meta-analysis stratified by ethnicity and age also revealed no association between asthma and these polymorphisms. Furthermore, no association was found between asthma and the CCC and TCT haplotypes of PTGDR, and meta-analysis stratified by ethnicity and age revealed no association between asthma and the CCC and TCT PTGDR haplotypes. This meta-analysis demonstrates that the PTGDR -549 C/T polymorphism confers susceptibility to asthma in Europeans and adults. However, no association was found between the PTGDR 441 C/T and -197 C/T polymorphisms or the CCC and TCT haplotypes and asthma susceptibility.

摘要

本研究旨在探讨前列腺素 D2 受体(PTGDR)多态性是否与哮喘易感性相关。采用等位基因对比、隐性模型、显性模型和加性模型,对 PTGDR-549C/T、-441C/T 和-197C/T 多态性与哮喘的相关性进行了荟萃分析:(1)等位基因对比;(2)隐性模型;(3)显性模型;(4)加性模型。按照-549/-441/-179 顺序构建了三个多态性单体型。对转录活性高的单体型 CCC(-549C/-441C/-179C)和转录活性低的单体型 TCT(-549T/-441T/-179T)进行了荟萃分析。本荟萃分析共纳入了 9 篇文献中的 13 项独立对照研究,包括 7155 例哮喘患者和 7285 例对照。结果显示,在等位基因对比中,PTGDR-549C/T 多态性与哮喘相关(OR=1.133,95%CI=1.004-1.279,P=0.043)。按种族进行亚组分析显示,在欧洲人群中,PTGDR-549C 等位基因与哮喘相关(OR=1.192,95%CI=1.032-1.377,P=0.017)。进一步对年龄进行分层分析显示,PTGDR-549C 等位基因与成人哮喘相关(OR=1.248,95%CI=1.076-1.447,P=0.003),但与儿童哮喘无关(OR=0.933,95%CI=0.756-1.154,P=0.324)。显性和加性模型分析显示出与 PTGDR-549C 等位基因相似的模式,即欧洲人和成年人中存在显著相关性,但在儿童中无相关性。PTGDR-441C/T 和-197C/T 多态性与哮喘无相关性,亚组分析也未显示出这些多态性与哮喘之间存在相关性。PTGDR-549C/T 多态性与哮喘易感性相关,但未发现与 CCC 和 TCT 单体型相关,且亚组分析也未发现与 CCC 和 TCT 单体型相关。本荟萃分析表明,PTGDR-549C/T 多态性与欧洲人和成年人的哮喘易感性相关。然而,PTGDR-441C/T 和-197C/T 多态性或 CCC 和 TCT 单体型与哮喘易感性无相关性。

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