Autoimmune diseases and COPD risk: A Mendelian randomization study

被引:0
作者
Ma, Xinlai [1 ]
Sun, Yuxiao [1 ]
Mou, Hongyu [1 ]
Zhang, Wei [2 ]
机构
[1] Shandong Univ Tradit Chinese Med, Clin Med Coll 1, Jinan, Peoples R China
[2] Shandong Univ Tradit Chinese Med, Affiliated Hosp, Dept Pulm & Crit Care Med, Jinan, Peoples R China
关键词
Autoimmune diseases; COPD; Mendelian randomization; OBSTRUCTIVE PULMONARY-DISEASE; MULTIPLE GENETIC-VARIANTS; EPIDEMIOLOGY; PATHOGENESIS;
D O I
10.1016/j.intimp.2024.112791
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Studies in epidemiology have indicated a link between chronic obstructive pulmonary disease (COPD) and various autoimmune conditions.This study aimed to investigate the potential causal link between nine autoimmune diseases with a genetic basis and COPD using a two-sample Mendelian randomization (MR) analysis. Method: To test the impact of susceptibility to immune-related outcomes on genetic prediction of COPD risk, we used pooled statistics from the largest genome-wide association study (GWAS) in Europe in a two-sample MR setting.Genetic data for type 1 diabetes, hypothyroidism, systemic lupus erythematosus, and primary biliary cirrhosis were obtained from the European Bioinformatics Institute (EBI), while data for multiple sclerosis and primary sclerosing cholangitis were extracted from the Integrative Epidemiology Unit (IEU) database. Additionally, genetic data for ulcerative colitis, rheumatoid arthritis, and celiac disease were also collected.These nine autoimmune diseases and the COPD cohort from the UK Biobank (1605 cases and 461,328 controls) were analyzed separately as exposure and outcome.Our primary method for the initial screening was inverse variance weighting (IVW).The MR-Egger regression test assessed multivariate validity, while the Cochran's Q test examined heterogeneity.To ensure the reliability of the findings, a leave-one-out analysis was conducted. Result: IVW discovered proof of type 1 diabetes (OR = 1.0003; 95 % CI = 1.0000-1.0005; P = 0.046), hypothyroidism (OR = 1.0004; 95 % CI = 1.0001-1.0008; P = 0.0263), celiac disease (OR = 1.0002; 95 % CI = 1.0000-1.0004; P = 0.0168) and systemic lupus erythematosus (OR = 1.0002; 95 % CI = 1.0000-1.0004; P = 0.049) were significantly linked to the heightened risk of COPD with no signs of variation or pleiotropy.Even after accounting for potential confounding factors like smoking, the correlation remained robust.Additionally, our research found that the IVW method did not indicate any causal link between COPD and multiple sclerosis, ulcerative colitis, rheumatoid arthritis, primary biliary cirrhosis, or primary sclerosing cholangitis (all P >0.05). Conclusion: This research discovered that individuals with type 1 diabetes, hypothyroidism, celiac disease, and systemic lupus erythematosus have a higher likelihood of developing COPD.Additionally, this research revealed no connection between COPD and multiple sclerosis, ulcerative colitis, rheumatoid arthritis, primary biliary cirrhosis, or primary sclerosing cholangitis.
引用
收藏
页数:8
相关论文
共 25 条
[1]   Clinical, radiologic, and induced sputum features of chronic obstructive pulmonary disease in nonsmokers - A descriptive study [J].
Birring, SS ;
Brightling, CE ;
Bradding, P ;
Entwisle, JJ ;
Vara, DD ;
Grigg, J ;
Wardlaw, AJ ;
Pavord, ID .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (08) :1078-1083
[2]   Inferring Causal Relationships Between Risk Factors and Outcomes from Genome-Wide Association Study Data [J].
Burgess, Stephen ;
Foley, Christopher N. ;
Zuber, Verena .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 19, 2018, 19 :303-327
[3]   Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data [J].
Burgess, Stephen ;
Butterworth, Adam ;
Thompson, Simon G. .
GENETIC EPIDEMIOLOGY, 2013, 37 (07) :658-665
[4]   Avoiding bias from weak instruments in Mendelian randomization studies [J].
Burgess, Stephen ;
Thompson, Simon G. .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2011, 40 (03) :755-764
[5]   Autoimmunity and COPD Clinical Implications [J].
Caramori, Gaetano ;
Ruggeri, Paolo ;
Di Stefano, Antonino ;
Mumby, Sharon ;
Girbino, Giuseppe ;
Adcock, Ian M. ;
Kirkham, Paul .
CHEST, 2018, 153 (06) :1424-1431
[6]   Definition and Nomenclature of Chronic Obstructive Pulmonary Disease Time for Its Revision [J].
Celli, Bartolome ;
Fabbri, Leonardo ;
Criner, Gerard ;
Martinez, Fernando J. ;
Mannino, David ;
Vogelmeier, Claus ;
Montes de Oca, Maria ;
Papi, Alberto ;
Sin, Don D. ;
Han, MeiLan K. ;
Agusti, Alvar .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2022, 206 (11) :1317-1325
[7]   Revisiting the genome-wide significance threshold for common variant GWAS [J].
Chen, Zhongsheng ;
Boehnke, Michael ;
Wen, Xiaoquan ;
Mukherjee, Bhramar .
G3-GENES GENOMES GENETICS, 2021, 11 (02)
[8]   Risk of Peripheral Arterial Occlusive Disease in Patients With Systemic Lupus Erythematosus A Nationwide Population-Based Cohort Study [J].
Chuang, Ya-Wen ;
Yu, Mei-Ching ;
Lin, Cheng-Li ;
Yu, Tung-Min ;
Shu, Kuo-Hsiung ;
Kao, Chia-Hung .
MEDICINE, 2015, 94 (46) :e2121
[9]   Overview of the Epidemiology Methods and Applications: Strengths and Limitations of Observational Study Designs [J].
Colditz, Graham A. .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 2010, 50 :10-12
[10]   MECHANISMS OF DISEASE Immunologic Aspects of Chronic Obstructive Pulmonary Disease [J].
Cosio, Manuel G. ;
Saetta, Marina ;
Agusti, Alvar .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (23) :2445-2454