{"title":"评估慢性阻塞性肺疾病和肺结核之间的因果关系:一项孟德尔随机研究。","authors":"Zhuo Wang, Shuang Zhao, Yiwu Zhou, Yanqi He","doi":"10.2147/COPD.S511734","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Chronic obstructive pulmonary disease (COPD) and tuberculosis are both significant global public health challenges. The co-occurrence of these two diseases is frequently observed in clinical settings. However, their causal relationship remains unclear.</p><p><strong>Methods: </strong>We utilized genome-wide association study (GWAS) datasets to conduct bidirectional two-sample Mendelian randomization and multivariable Mendelian randomization analyses. We first analyzed COPD data from the FinnGen consortium (n = 193,638) and tuberculosis data from a genetic association study (n = 484,598). In the second phase, we stratified COPD patients by age into the EARLY COPD group (Event_Age < 65) and the LATER COPD group (Event_Age ≥ 65) to explore their causal relationships with tuberculosis separately. We then validated these results using tuberculosis data from MRC-IEU (n = 462,933). Finally, smoking and COPD-related SNPs as instrumental variables were analyzed by multivariable Mendelian randomization to further investigate the association between COPD and tuberculosis. Multiple methods were used in the Mendelian analyses to ensure a comprehensive and rigorous investigation.</p><p><strong>Results: </strong>In the initial analysis phase utilizing the inverse variance weighting (IVW) method, tuberculosis showed no significant contribution to the incidence of COPD (IVW odds ratio (OR) = 0.9961; 95% confidence interval (CI) = 0.9828-1.0095; P = 0.564). Conversely, COPD appeared to significantly increase the risk of developing tuberculosis (IVW OR = 1.0008; 95% CI = 1.0001-1.0014; P = 0.015), particularly in patients under 65 (IVW OR = 1.0008; P = 0.011).</p><p><strong>Conclusion: </strong>This Mendelian randomization analysis found that COPD may increase the risk of tuberculosis, while tuberculosis does not increase the risk of COPD, suggesting the necessity of enhancing prevention and screening efforts for tuberculosis among COPD patients, especially younger individuals.</p>","PeriodicalId":48818,"journal":{"name":"International Journal of Chronic Obstructive Pulmonary Disease","volume":"20 ","pages":"1361-1371"},"PeriodicalIF":2.7000,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12065539/pdf/","citationCount":"0","resultStr":"{\"title\":\"Assessing the Causal Relationship between Chronic Obstructive Pulmonary Disease and Tuberculosis: A Mendelian Randomization Study.\",\"authors\":\"Zhuo Wang, Shuang Zhao, Yiwu Zhou, Yanqi He\",\"doi\":\"10.2147/COPD.S511734\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Chronic obstructive pulmonary disease (COPD) and tuberculosis are both significant global public health challenges. 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引用次数: 0
摘要
背景:慢性阻塞性肺疾病(COPD)和结核病都是重大的全球公共卫生挑战。这两种疾病的同时发生在临床上是很常见的。然而,它们之间的因果关系尚不清楚。方法:利用全基因组关联研究(GWAS)数据集进行双向双样本孟德尔随机化和多变量孟德尔随机化分析。我们首先分析了来自FinnGen联盟的COPD数据(n = 193,638)和来自遗传关联研究的结核病数据(n = 484,598)。在第二阶段,我们将COPD患者按年龄分层分为早期COPD组(Event_Age < 65)和晚期COPD组(Event_Age≥65),分别探讨其与结核病的因果关系。然后,我们使用MRC-IEU的结核病数据验证了这些结果(n = 462,933)。最后,通过多变量孟德尔随机化分析吸烟和COPD相关snp作为工具变量,进一步研究COPD与结核病的相关性。在孟德尔分析中使用了多种方法,以确保全面和严格的调查。结果:在使用逆方差加权(IVW)方法的初始分析阶段,结核病对COPD的发病率没有显著贡献(IVW优势比(OR) = 0.9961;95%置信区间(CI) = 0.9828-1.0095;P = 0.564)。相反,COPD似乎显著增加发生结核病的风险(IVW OR = 1.0008;95% ci = 1.0001-1.0014;P = 0.015),尤其是65岁以下的患者(IVW OR = 1.0008;P = 0.011)。结论:本孟德尔随机化分析发现,COPD可能增加结核病的风险,而结核病不会增加COPD的风险,提示有必要加强COPD患者,特别是年轻人对结核病的预防和筛查。
Assessing the Causal Relationship between Chronic Obstructive Pulmonary Disease and Tuberculosis: A Mendelian Randomization Study.
Background: Chronic obstructive pulmonary disease (COPD) and tuberculosis are both significant global public health challenges. The co-occurrence of these two diseases is frequently observed in clinical settings. However, their causal relationship remains unclear.
Methods: We utilized genome-wide association study (GWAS) datasets to conduct bidirectional two-sample Mendelian randomization and multivariable Mendelian randomization analyses. We first analyzed COPD data from the FinnGen consortium (n = 193,638) and tuberculosis data from a genetic association study (n = 484,598). In the second phase, we stratified COPD patients by age into the EARLY COPD group (Event_Age < 65) and the LATER COPD group (Event_Age ≥ 65) to explore their causal relationships with tuberculosis separately. We then validated these results using tuberculosis data from MRC-IEU (n = 462,933). Finally, smoking and COPD-related SNPs as instrumental variables were analyzed by multivariable Mendelian randomization to further investigate the association between COPD and tuberculosis. Multiple methods were used in the Mendelian analyses to ensure a comprehensive and rigorous investigation.
Results: In the initial analysis phase utilizing the inverse variance weighting (IVW) method, tuberculosis showed no significant contribution to the incidence of COPD (IVW odds ratio (OR) = 0.9961; 95% confidence interval (CI) = 0.9828-1.0095; P = 0.564). Conversely, COPD appeared to significantly increase the risk of developing tuberculosis (IVW OR = 1.0008; 95% CI = 1.0001-1.0014; P = 0.015), particularly in patients under 65 (IVW OR = 1.0008; P = 0.011).
Conclusion: This Mendelian randomization analysis found that COPD may increase the risk of tuberculosis, while tuberculosis does not increase the risk of COPD, suggesting the necessity of enhancing prevention and screening efforts for tuberculosis among COPD patients, especially younger individuals.
期刊介绍:
An international, peer-reviewed journal of therapeutics and pharmacology focusing on concise rapid reporting of clinical studies and reviews in COPD. Special focus will be given to the pathophysiological processes underlying the disease, intervention programs, patient focused education, and self management protocols. This journal is directed at specialists and healthcare professionals