The genetic etiology of body fluids on chronic obstructive airways disease

Abstract Background Numerous studies have documented significant alterations in the bodily fluids of Chronic Obstructive Pulmonary Disease (COPD) patients. However, existing literature lacks causal inference due to residual confounding and reverse causality. Methods Summary-level data for COPD were...

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Main Authors: Zhangkai J. Cheng, Haojie Wu, Zhenglin Chang, Jiahao Cheng, Suilin Wang, Changlian Liu, Yanxi Zhang, Shiliang Xu, Qiongqiong Wan, JinWen Ron, Kemin Liu, Baoqing Sun
Format: Article
Language:English
Published: BMC 2024-01-01
Series:Respiratory Research
Subjects:
Online Access:https://doi.org/10.1186/s12931-023-02661-6
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author Zhangkai J. Cheng
Haojie Wu
Zhenglin Chang
Jiahao Cheng
Suilin Wang
Changlian Liu
Yanxi Zhang
Shiliang Xu
Qiongqiong Wan
JinWen Ron
Kemin Liu
Baoqing Sun
author_facet Zhangkai J. Cheng
Haojie Wu
Zhenglin Chang
Jiahao Cheng
Suilin Wang
Changlian Liu
Yanxi Zhang
Shiliang Xu
Qiongqiong Wan
JinWen Ron
Kemin Liu
Baoqing Sun
author_sort Zhangkai J. Cheng
collection DOAJ
description Abstract Background Numerous studies have documented significant alterations in the bodily fluids of Chronic Obstructive Pulmonary Disease (COPD) patients. However, existing literature lacks causal inference due to residual confounding and reverse causality. Methods Summary-level data for COPD were obtained from two national biobanks: the UK Biobank, comprising 1,605 cases and 461,328 controls, and FinnGen, with 6,915 cases and 186,723 controls. We also validated our findings using clinical data from 2,690 COPD patients and 3,357 healthy controls from the First Affiliated Hospital of Guangzhou Medical University. A total of 44 bodily fluid biomarkers were selected as candidate risk factors. Mendelian randomization (MR) and meta-analyses were used to evaluate the causal effects of these bodily fluids on COPD and lung function (FEV1/FVC). Results Mendelian randomization (MR) and meta-analyses, by integrating data from the UK Biobank and FinnGen cohort, found that 3 bodily fluids indicators (HDLC, EOS, and TP) were causally associated with the risk of COPD, two (EOS and TP) of which is consistent with our observational findings. Moreover, we noticed EOS and TP were causally associated with the risk of lung function (FEV1/FVC). Conclusions The MR findings and clinical data highlight the independent and significant roles of EOS and TP in the development of COPD and lung function (FEV1/FVC), which might provide a deeper insight into COPD risk factors and supply potential preventative strategies.
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spelling doaj.art-c4c89073e3064a47a3da606a8edffdaa2024-01-21T12:31:19ZengBMCRespiratory Research1465-993X2024-01-012511910.1186/s12931-023-02661-6The genetic etiology of body fluids on chronic obstructive airways diseaseZhangkai J. Cheng0Haojie Wu1Zhenglin Chang2Jiahao Cheng3Suilin Wang4Changlian Liu5Yanxi Zhang6Shiliang Xu7Qiongqiong Wan8JinWen Ron9Kemin Liu10Baoqing Sun11Department of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityGuangzhou University of Chinese MedicineDepartment of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityDepartment of Clinical Laboratory, National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical UniversityAbstract Background Numerous studies have documented significant alterations in the bodily fluids of Chronic Obstructive Pulmonary Disease (COPD) patients. However, existing literature lacks causal inference due to residual confounding and reverse causality. Methods Summary-level data for COPD were obtained from two national biobanks: the UK Biobank, comprising 1,605 cases and 461,328 controls, and FinnGen, with 6,915 cases and 186,723 controls. We also validated our findings using clinical data from 2,690 COPD patients and 3,357 healthy controls from the First Affiliated Hospital of Guangzhou Medical University. A total of 44 bodily fluid biomarkers were selected as candidate risk factors. Mendelian randomization (MR) and meta-analyses were used to evaluate the causal effects of these bodily fluids on COPD and lung function (FEV1/FVC). Results Mendelian randomization (MR) and meta-analyses, by integrating data from the UK Biobank and FinnGen cohort, found that 3 bodily fluids indicators (HDLC, EOS, and TP) were causally associated with the risk of COPD, two (EOS and TP) of which is consistent with our observational findings. Moreover, we noticed EOS and TP were causally associated with the risk of lung function (FEV1/FVC). Conclusions The MR findings and clinical data highlight the independent and significant roles of EOS and TP in the development of COPD and lung function (FEV1/FVC), which might provide a deeper insight into COPD risk factors and supply potential preventative strategies.https://doi.org/10.1186/s12931-023-02661-6COPDBodily fluidsMendelian randomizationGenome-wide analysis
spellingShingle Zhangkai J. Cheng
Haojie Wu
Zhenglin Chang
Jiahao Cheng
Suilin Wang
Changlian Liu
Yanxi Zhang
Shiliang Xu
Qiongqiong Wan
JinWen Ron
Kemin Liu
Baoqing Sun
The genetic etiology of body fluids on chronic obstructive airways disease
Respiratory Research
COPD
Bodily fluids
Mendelian randomization
Genome-wide analysis
title The genetic etiology of body fluids on chronic obstructive airways disease
title_full The genetic etiology of body fluids on chronic obstructive airways disease
title_fullStr The genetic etiology of body fluids on chronic obstructive airways disease
title_full_unstemmed The genetic etiology of body fluids on chronic obstructive airways disease
title_short The genetic etiology of body fluids on chronic obstructive airways disease
title_sort genetic etiology of body fluids on chronic obstructive airways disease
topic COPD
Bodily fluids
Mendelian randomization
Genome-wide analysis
url https://doi.org/10.1186/s12931-023-02661-6
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