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辽宁地区 pri-let-7f 基因遗传多态性、基因-环境和基因-基因相互作用与缺血性脑卒中风险的相关性研究

Genetic polymorphisms of pri-let-7f, gene-environment and gene-gene interactions, and associations with ischemic stroke risk in Liaoning Province.

机构信息

Department of Neurology, Key Laboratory for Neurological Big Data of Liaoning Province, The First Affiliated Hospital of China Medical University, Shenyang, China.

Department of Neurology, China-Japan Friendship Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.

出版信息

J Int Med Res. 2023 May;51(5):3000605231173578. doi: 10.1177/03000605231173578.

Abstract

OBJECTIVE

The incidence of stroke has been rising annually and investigations into traditional risk factors have led to increased attention on genetic factors. In this study, we focused on the pri-let-7f gene, and investigated the association between pri-let-7f gene polymorphisms and ischemic stroke (IS).

METHODS

This case-control study included 1803 patients and 1456 healthy controls of Han ethnicity living in Liaoning Province. We carried out genotyping analysis of two loci, pri-let-7f-1 rs10739971 and pri-let-7f-2 rs17276588, and performed statistical analysis controlling for confounding factors by logistic regression.

RESULTS

The A alleles and AA genotypes of both loci were significantly associated with an increased risk of IS. Variant genotypes of rs17276588 may also increase the risk of IS in females with alcohol intake. Gene-gene interaction analysis showed combined effects of mutations in both these single nucleotide polymorphisms (SNPs).

CONCLUSIONS

This study demonstrated an association between pri-let-7f SNPs and IS, providing potential latent biomarkers for the risk of IS. However, more detailed studies are needed to clarify these results.

摘要

目的

中风的发病率逐年上升,对传统危险因素的研究使得人们越来越关注遗传因素。本研究聚焦 pri-let-7f 基因,探讨 pri-let-7f 基因多态性与缺血性脑卒中(IS)的关系。

方法

本病例对照研究纳入了来自辽宁省的 1803 例患者和 1456 例汉族健康对照。我们对两个位点 pri-let-7f-1 rs10739971 和 pri-let-7f-2 rs17276588 进行了基因分型分析,并通过 logistic 回归控制混杂因素进行了统计分析。

结果

两个位点的 A 等位基因和 AA 基因型均与 IS 风险增加显著相关。rs17276588 的变异基因型也可能增加有饮酒史女性发生 IS 的风险。基因-基因交互作用分析显示这两个单核苷酸多态性(SNP)的突变存在联合效应。

结论

本研究表明 pri-let-7f SNP 与 IS 之间存在关联,为 IS 风险提供了潜在的潜在生物标志物。然而,需要更详细的研究来阐明这些结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a3/10184219/94a6e994e8f4/10.1177_03000605231173578-fig1.jpg

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