关节病变与产后出血的关系:一项双向孟德尔随机研究。

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY Frontiers in Genetics Pub Date : 2024-12-11 eCollection Date: 2024-01-01 DOI:10.3389/fgene.2024.1448754
Zhao Wu, Chengyu Yuan, Xue Peng
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引用次数: 0

摘要

背景:研究将关节病与不良妊娠结局联系起来。本研究旨在通过孟德尔随机化(MR)分析探讨其与产后出血(PPH)的关系。方法:研究使用IEU OpenGWAS数据库中PPH和关节病的GWAS数据。选择工具变量后,采用MR- egger、加权中位数、简单模式、加权模式和IVW方法进行双向磁共振分析。然后进行敏感性分析以评估MR结果的可靠性。最后,对前向MR中关节病snp对应的基因进行富集分析,探索其生物学功能和信号通路。结果:正向磁共振结果显示,关节病变与PPH有因果关系,关节病变是PPH的危险因素。然而,通过反向MR分析,PPH和关节病变之间没有因果关系。通过敏感性分析说明MR分析结果的可靠性,无异质性、水平多效性和LOO分析的严重偏倚snp。此外,共获得33个与关节病snp相关的基因,这些基因主要富集于调控生物刺激应答、剪接体snRNP复合物和GO连接酶活性,以及自然杀伤细胞介导的KEGG通路细胞毒性。结论:本研究支持关节病是PPH的危险因素,并分析了snp对应基因的通路,为进一步探讨关节病与PPH的分子机制提供重要参考和证据。
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Association between arthropathies and postpartum hemorrhage: a bidirectional Mendelian randomization study.

Background: Research links arthropathies with adverse pregnancy outcomes. This study aims to explore its connection to postpartum hemorrhage (PPH) through Mendelian randomization (MR) analysis.

Methods: The study used GWAS data from the IEU OpenGWAS database for PPH and arthropathies. After selecting instrumental variables, bidirectional MR analysis was conducted using MR-Egger, Weighted median, Simple mode, Weighted mode, and IVW methods. Sensitivity analysis was then performed to assess MR results reliability. Finally, enrichment analysis of genes corresponding to arthropathies SNPs in forward MR was conducted to explore their biological function and signaling pathways.

Results: The forward MR results revealed that arthropathies was causally related to PPH, and arthropathies was a risk factor for PPH. Whereas, there was not a causal relationship between PPH and arthropathies by reverse MR analysis. It illustrated the reliability of the MR analysis results by the sensitivity analysis without heterogeneity, horizontal pleiotropy, and SNPs of severe bias by LOO analysis. Furthermore, a total of 33 genes corresponding to SNPs of arthropathies were obtained, which were mainly enriched in regulation of response to biotic stimulus, spliceosomal snRNP complex and ligase activity in GO terms, and natural killer cell-mediated cytotoxicity in KEGG pathways.

Conclusion: This study supported that arthropathies was a risk factor for PPH, and the pathways involved the genes corresponding to SNPs were analyzed, which could provide important reference and evidence for further exploring the molecular mechanism between arthropathies and PPH.

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来源期刊
Frontiers in Genetics
Frontiers in Genetics Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
5.50
自引率
8.10%
发文量
3491
审稿时长
14 weeks
期刊介绍: Frontiers in Genetics publishes rigorously peer-reviewed research on genes and genomes relating to all the domains of life, from humans to plants to livestock and other model organisms. Led by an outstanding Editorial Board of the world’s leading experts, this multidisciplinary, open-access journal is at the forefront of communicating cutting-edge research to researchers, academics, clinicians, policy makers and the public. The study of inheritance and the impact of the genome on various biological processes is well documented. However, the majority of discoveries are still to come. A new era is seeing major developments in the function and variability of the genome, the use of genetic and genomic tools and the analysis of the genetic basis of various biological phenomena.
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