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采用双向孟德尔随机化方法揭示慢性阻塞性肺疾病及其常见合并症之间的因果关系。

Unraveling the causality between chronic obstructive pulmonary disease and its common comorbidities using bidirectional Mendelian randomization.

机构信息

Department of Respiratory and Critical Care Medicine, Peking University Third Hospital; Research Center for Chronic Airway Diseases, Peking University Health Science Center, Beijing, China.

出版信息

Eur J Med Res. 2024 Feb 26;29(1):143. doi: 10.1186/s40001-024-01686-x.

Abstract

BACKGROUND

Chronic obstructive pulmonary disease (COPD) frequently coexists with various diseases, yet the causal relationship between COPD and these comorbidities remains ambiguous. As a result, the aim of our study is to elucidate the potential causality between COPD and its common comorbidities.

METHODS

We employed the Mendelian randomization (MR) method to analyze single nucleotide polymorphism (SNP) data of common comorbidities with COPD from FinnGen and Integrative Epidemiology Unit (IEU) databases. Causality was primarily assessed using the inverse variance weighting (IVW) method. Multivariable Mendelian randomization (MVMR) analysis was also conducted to eliminate the interference of smoking-related phenotypes. Sensitivity analysis was conducted to ensure the reliability of our findings.

RESULTS

Preliminary univariable MR revealed an increased risk of lung squamous cell carcinoma (LUSC) (IVW: OR = 1.757, 95% CI = 1.162-2.657, P = 0.008), chronic kidney disease (CKD) (IVW: OR = 1.193, 95% CI = 1.072-1.326, P < 0.001), chronic periodontitis (IVW: OR = 1.213, 95% CI = 1.038-1.417, P = 0.012), and heart failure (HF) (IVW: OR = 1.127, 95% CI = 1.043-1.218, P = 0.002). Additionally, the reverse MR analysis indicated that genetic susceptibility to HF (IVW: OR = 1.272, 95% CI = 1.084-1.493, P = 0.003), obesity (IVW: OR = 1.128, 95% CI = 1.056-1.205, P < 0.001), depression (IVW: OR = 1.491, 95% CI = 1.257-1.770, P < 0.001), and sleep apnea syndrome (IVW: OR = 1.209, 95% CI = 1.087-1.345, P < 0.001) could raise the risk of COPD. The MVMR analysis showed no causal effect of COPD on susceptibility to chronic periodontitis after adjusting for smoking.

CONCLUSIONS

Our study identified that COPD may elevate the risk of LUSC, HF, and CKD. Additionally, our analysis revealed that HF, sleep apnea symptoms, depression, and obesity might also increase the susceptibility to COPD. These findings revealed a potential causal relationship between COPD and several prevalent comorbidities, which may provide new insights for disease early prediction and prevention.

摘要

背景

慢性阻塞性肺疾病(COPD)常与多种疾病共存,但 COPD 与这些合并症之间的因果关系仍不清楚。因此,我们的研究旨在阐明 COPD 与其常见合并症之间的潜在因果关系。

方法

我们使用孟德尔随机化(MR)方法分析了 FinnGen 和整合流行病学单位(IEU)数据库中 COPD 常见合并症的单核苷酸多态性(SNP)数据。主要使用逆方差加权(IVW)法评估因果关系。还进行了多变量孟德尔随机化(MVMR)分析,以消除与吸烟相关表型的干扰。进行敏感性分析以确保研究结果的可靠性。

结果

初步单变量 MR 显示肺鳞状细胞癌(LUSC)(IVW:OR=1.757,95%CI=1.162-2.657,P=0.008)、慢性肾脏病(CKD)(IVW:OR=1.193,95%CI=1.072-1.326,P<0.001)、慢性牙周炎(IVW:OR=1.213,95%CI=1.038-1.417,P=0.012)和心力衰竭(HF)(IVW:OR=1.127,95%CI=1.043-1.218,P=0.002)的风险增加。此外,反向 MR 分析表明 HF(IVW:OR=1.272,95%CI=1.084-1.493,P=0.003)、肥胖(IVW:OR=1.128,95%CI=1.056-1.205,P<0.001)、抑郁(IVW:OR=1.491,95%CI=1.257-1.770,P<0.001)和睡眠呼吸暂停综合征(IVW:OR=1.209,95%CI=1.087-1.345,P<0.001)的遗传易感性可能会增加 COPD 的风险。MVMR 分析表明,在调整吸烟因素后,COPD 对慢性牙周炎的易感性没有因果关系。

结论

我们的研究发现 COPD 可能会增加肺鳞状细胞癌、HF 和 CKD 的风险。此外,我们的分析还表明,HF、睡眠呼吸暂停症状、抑郁和肥胖也可能增加 COPD 的易感性。这些发现揭示了 COPD 与几种常见合并症之间的潜在因果关系,这可能为疾病的早期预测和预防提供新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9596/10895842/bf62a8d696da/40001_2024_1686_Fig1_HTML.jpg

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