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白细胞介素-18基因多态性缺陷与哮喘风险的关联:一项更新的荟萃分析。

Interleukin-18 Polymorphisms Deficiency Association with Asthma Risk: An Update Meta-analysis.

作者信息

Liu Huan, Feng Yu, Zhang Wei, Deng Xiao-Dong, Ma Ying, Liu Yun

机构信息

Department of Preventive Medicine, North Sichuan Medical College, Nanchong, Sichuan, China AND Department of Forensic Medicine, North Sichuan Medical College, Nanchong, Sichuan, China.

Department of Criminal Science and Technology, Chongqing Police College, Chongqing, China.

出版信息

Iran J Allergy Asthma Immunol. 2019 Jun 8;18(3):251-261. doi: 10.18502/ijaai.v18i3.1118.

Abstract

Growing evidence indicated conflicting results that Interleukin-18 (IL-18) promoter polymorphisms rs1946518 (A-607C), rs187238 (G-137C) and rs549908 (A-105C) were associated with asthma risk. The aim of this study is to comprehensively evaluate the IL-18 polymorphisms and asthma by a systematic review and meta-analysis. A total of 12 studies testing the association between these polymorphisms and asthma were examined (8 studies for A-607C, 8 studies for G-137C, and 4 studies for A-105C) in the update meta-analysis, up to Dec 30, 2017. Summary odds ratios (ORs) and 95% confidence intervals (CI) were used to estimate the strength of association between each polymorphism and asthma using fixed- and random-effects models when appropriate. Heterogeneity and publication bias were evaluated. The meta-analysis results indicated that any allele frequencies of the IL-18 polymorphisms (A-607C, G-137C and A-105C) was not associated with asthma risk (p>0.05). And no statistically significant association was observed between genotype frequencies of these polymorphisms and asthma under different genetic models (p>0.05). Subgroup analysis results were similar to the main analysis by ethnicity, sample size, genotyping methods, matching criteria and quality score. There was no evidence of publication bias. The present meta-analysis suggests that IL-18 polymorphisms (A-607C, G-137C and A-105C) were unlikely to be associated with asthma risk.

摘要

越来越多的证据表明,白细胞介素-18(IL-18)启动子多态性rs1946518(A-607C)、rs187238(G-137C)和rs549908(A-105C)与哮喘风险之间的关联结果相互矛盾。本研究的目的是通过系统评价和荟萃分析全面评估IL-18多态性与哮喘的关系。在截至2017年12月30日的更新荟萃分析中,共检查了12项检测这些多态性与哮喘之间关联的研究(8项针对A-607C,8项针对G-137C,4项针对A-105C)。当合适时,使用固定效应模型和随机效应模型,通过汇总比值比(OR)和95%置信区间(CI)来估计每种多态性与哮喘之间关联的强度。评估了异质性和发表偏倚。荟萃分析结果表明,IL-18多态性(A-607C、G-137C和A-105C)的任何等位基因频率均与哮喘风险无关(p>0.05)。在不同遗传模型下,这些多态性的基因型频率与哮喘之间未观察到统计学上的显著关联(p>0.05)。按种族、样本量、基因分型方法、匹配标准和质量评分进行的亚组分析结果与主要分析结果相似。没有发表偏倚的证据。本荟萃分析表明,IL-18多态性(A-607C、G-137C和A-105C)不太可能与哮喘风险相关。

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