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甘露聚糖结合凝集素基因多态性与复发性外阴阴道感染风险的荟萃分析。

A meta-analysis of mannose-binding lectin gene polymorphisms with the risk of recurrent vulvovaginal infections.

机构信息

Department of Molecular Biology & Biochemistry, Guru Nanak Dev University, Amritsar, India.

Department of Information Technology, University of Turku, Turku, Finland.

出版信息

Sci Rep. 2020 Apr 8;10(1):6079. doi: 10.1038/s41598-020-63261-8.

Abstract

The genetic variants of Mannose-Binding Lectin, a vital component of innate immunity have been studied with acute/recurrent vaginal infections ((R)VVI) and presented inconclusive findings. Therefore, a systematic review and meta-analysis of published data were conducted to assess the possible role of these variations in (R)VVI. A comprehensive search was made using PubMed, Web of Science and Google scholar till June 18, 2019. A total of 12 studies met the specified criteria and were included in the analysis. Different comparisons were made on the basis of the outcome of interest that resulted in the filtering of studies for the pooled analysis to find an association using the standard genetic models. Odds ratio (OR) with 95% confidence interval (CI) was chosen as the effect measure for the data synthesis. The trim and fill technique was applied to adjust the publication bias. The meta-analysis revealed the significant association (p < 0.05) of rs1800450 polymorphism with RVVI risk (OR ≥ 3.5) in all the genetic models. The subgroup analysis identified the same association in Caucasian and Mixed ethnicity. Quantitative synthesis based on RVVC showed>3.5 fold risk of disease development accredited to rs1800450. A combined evaluation of Exon1 variants showed no association with (R)VVI. This meta-analysis suggests rs1800450 polymorphism as a genetic predisposing factor for RVVI, but to reinforce, further studies with a larger sample size are warranted.

摘要

甘露糖结合凝集素的遗传变异是先天免疫的重要组成部分,已经针对急性/复发性阴道感染 (R)VVI 进行了研究,但结果尚无定论。因此,进行了系统的文献回顾和荟萃分析,以评估这些变异与 (R)VVI 之间可能存在的关联。使用 PubMed、Web of Science 和 Google Scholar 进行了全面的搜索,截至 2019 年 6 月 18 日。共有 12 项符合特定标准的研究被纳入分析。根据感兴趣的结果进行了不同的比较,导致对研究进行了过滤,以便使用标准遗传模型对汇总分析进行关联。选择比值比 (OR) 和 95%置信区间 (CI) 作为数据综合的效应度量。应用修剪和填充技术来调整发表偏倚。荟萃分析显示 rs1800450 多态性与 RVVI 风险之间存在显著关联 (p < 0.05),所有遗传模型的 OR 均≥3.5。亚组分析表明,在白种人和混合种族中也存在相同的关联。基于 RVVC 的定量综合表明,rs1800450 使疾病发展的风险增加了>3.5 倍。对 Exon1 变异的综合评估表明与 (R)VVI 无关联。这项荟萃分析表明 rs1800450 多态性是 RVVI 的遗传易感性因素,但为了加强证据,需要进行更大样本量的进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e866/7142065/25b774e9477d/41598_2020_63261_Fig1_HTML.jpg

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