探讨中国老年人CHRNA3基因中8个snp在COPD易感性中的作用。

IF 4.3
Annals of medicine Pub Date : 2025-12-01 Epub Date: 2025-03-12 DOI:10.1080/07853890.2025.2474726
Yamei Zheng, Jie Zhao, Meihua Liu, Yunchan Liu, Yipeng Ding, Tian Xie
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引用次数: 0

摘要

背景:慢性阻塞性肺疾病(COPD)是中国老年人发病和死亡的主要原因。遗传易感性是COPD的一个公认的危险因素,CHRNA3因其参与吸烟行为和肺功能而成为一个有希望的候选基因。本研究旨在探讨中国老年人群中8个CHRNA3 snp与COPD易感性的关系。方法:共纳入270例COPD患者和271例健康对照。使用Agena MassARRAY平台进行SNP基因分型。采用Logistic回归分析计算优势比(ORs)和95%置信区间(CIs)来评估snp与COPD风险之间的关系。使用Sangerbox软件生成森林图,以直观地表示关联结果。此外,使用Haploview 4.2软件构建单倍型块,以探索单倍型对COPD风险的潜在影响。结果:我们的研究结果表明rs615470、rs660652和rs472054与COPD风险降低相关,而rs8040868与风险增加相关。连锁不平衡(LD)分析鉴定出包含rs76071148、rs615470、rs660652、rs472054和rss578776的单倍型块。值得注意的是,单倍型TTAAG与COPD风险降低有关。结论:本研究为老年人COPD的遗传易感性,特别是snp在CHRNA3中的作用提供了有价值的见解。这些发现有助于更深入地了解COPD的发病机制,并可能有助于发现新的COPD治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Investigating the role of eight SNPs in <i>CHRNA3</i> for COPD susceptibility in the Chinese elderly population.

Investigating the role of eight SNPs in <i>CHRNA3</i> for COPD susceptibility in the Chinese elderly population.

Investigating the role of eight SNPs in <i>CHRNA3</i> for COPD susceptibility in the Chinese elderly population.

Investigating the role of eight SNPs in CHRNA3 for COPD susceptibility in the Chinese elderly population.

Background: Chronic obstructive pulmonary disease (COPD) is a leading cause of morbidity and mortality among the elderly in China. Genetic predisposition is a recognized risk factor for COPD, with CHRNA3 emerging as a promising candidate gene due to its involvement in smoking behavior and lung function. This study aimed to investigate the association between eight CHRNA3 SNPs and COPD susceptibility in the Chinese elderly population.

Methods: A total of 270 COPD patients and 271 healthy controls were included in the study. SNP genotyping was carried out using the Agena MassARRAY platform. Logistic regression analysis was employed to calculate odds ratios (ORs) and 95% confidence intervals (CIs) to assess the association between the SNPs and COPD risk. Forest plots were generated using Sangerbox software to visually represent the association results. Additionally, haplotype blocks were constructed using Haploview 4.2 software to explore the potential impact of haplotypes on COPD risk.

Results: Our findings indicated that rs615470, rs660652, and rs472054 are associated with a reduced risk of COPD, while rs8040868 is associated with an increased risk. Linkage disequilibrium (LD) analysis identified a haplotype block encompassing rs76071148, rs615470, rs660652, rs472054 and rs578776. Notably, the haplotype TTAAG was associated with a reduced risk of COPD.

Conclusion: This study provides valuable insights into the genetic susceptibility of COPD among the elderly, particularly regarding the role of SNPs in CHRNA3. These findings contribute to a deeper understanding of the pathogenesis of COPD and may facilitate the discovery of novel therapeutic targets for COPD.

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