Suppr超能文献

IL-27 基因 rs153109 和 rs17855750 多态性与子痫前期易感性和严重程度的关联:Meta 分析和试验序贯分析。

Association of IL-27 gene rs153109 and rs17855750 polymorphisms with preeclampsia susceptibility and severity: Meta-analysis and trial sequential analysis.

机构信息

Heart Medical Centre, First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.

Department of Physiology, Gannan Medical University, Ganzhou, Jiangxi, China.

出版信息

Medicine (Baltimore). 2023 Apr 21;102(16):e33578. doi: 10.1097/MD.0000000000033578.

Abstract

BACKGROUND

The aim of this meta-analysis is to evaluate the association of interleukin-27 gene rs153109 and rs17855750 polymorphisms with preeclampsia susceptibility and severity.

METHODS

Web of Science, PubMed, Embase, CBM, WanFang Data, CNKI, and VIP database were used for retrieving. After screening with our inclusion and exclusion criteria, data extraction and quantity evaluation were performed by 2 independent authors. Included case-control studies were used for meta-analysis by RevMan 5.4, and sensitivity analysis was carried out through 1-by-1 exclusion procedure. If heterogeneity exists, then random effects model was used; otherwise, fixed effect model was used. Publication bias analysis was performed using Begg test and Egger test. Trial sequential analysis was performed using trial sequential analysis 0.9.5.10 Beta.

RESULTS

A total of 5 articles were included. The heterogeneity was high across most models during the meta-analysis. Meta-analysis results related to preeclampsia susceptibility showed that P values of all the models were higher than .05, while for meta-analysis results related to preeclampsia severity showed that P values of all the models were higher than .05 except for TT versus TG + GG and TT versus TG models of rs17855750 group. The sensitivity of the meta-analysis was high, and trial sequential analysis showed the possibility of false negative results. No obvious publication bias was found.

CONCLUSIONS

There is no obvious association between interleukin-27 gene rs153109 and rs17855750 polymorphisms and preeclampsia susceptibility or severity. However, more multi-center and large sample case-control studies are expected to be carried out to verify our conclusion in the future.

摘要

背景

本荟萃分析旨在评估白细胞介素-27 基因 rs153109 和 rs17855750 多态性与子痫前期易感性和严重程度的关系。

方法

使用 Web of Science、PubMed、Embase、CBM、万方数据、中国知网和 VIP 数据库进行检索。根据纳入和排除标准进行筛选后,由 2 名独立作者进行数据提取和质量评估。采用 RevMan 5.4 对纳入的病例对照研究进行荟萃分析,如果存在异质性,则采用随机效应模型;否则,采用固定效应模型。采用 Begg 检验和 Egger 检验进行发表偏倚分析。采用 trial sequential analysis 0.9.5.10 Beta 进行试验序贯分析。

结果

共纳入 5 篇文章。荟萃分析中大多数模型的异质性较高。与子痫前期易感性相关的荟萃分析结果显示,所有模型的 P 值均高于.05,而与子痫前期严重程度相关的荟萃分析结果显示,除 rs17855750 组的 TT 与 TG + GG 和 TT 与 TG 模型外,所有模型的 P 值均高于.05。荟萃分析的敏感性较高,试验序贯分析显示存在假阴性结果的可能性。未发现明显的发表偏倚。

结论

白细胞介素-27 基因 rs153109 和 rs17855750 多态性与子痫前期易感性或严重程度之间无明显关联。然而,未来需要开展更多的多中心、大样本病例对照研究来验证我们的结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6feb/10118315/50771c9ab25d/medi-102-e33578-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验