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Lung function and onset of cardiometabolic diseases in the longitudinal Burden of Obstructive Lung Disease study

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dc.contributor Landspitali - The National University Hospital of Iceland
dc.contributor.author BOLD Collaborative Research Group
dc.date.accessioned 2025-02-17T01:03:01Z
dc.date.available 2025-02-17T01:03:01Z
dc.date.issued 2025-01-19
dc.identifier.citation BOLD Collaborative Research Group 2025, 'Lung function and onset of cardiometabolic diseases in the longitudinal Burden of Obstructive Lung Disease study', BMJ Open Respiratory Research, vol. 12, no. 1, e002442. https://doi.org/10.1136/bmjresp-2024-002442
dc.identifier.issn 2052-4439
dc.identifier.other 236091749
dc.identifier.other fab095b6-1fcb-4708-9104-ed2ccf5191e6
dc.identifier.other 85215838247
dc.identifier.other 39832891
dc.identifier.uri https://hdl.handle.net/20.500.11815/5338
dc.description Publisher Copyright: © 2025 Author(s) (or their employer(s)). Re-use permitted under CC BY. Published by BMJ Group.
dc.description.abstract Introduction Previous population-based studies, mainly from high-income countries, have shown that a higher forced vital capacity (FVC) is associated with a lower risk of developing cardiometabolic diseases. The aim of this study was to assess the longitudinal association between spirometry measures and the onset of cardiometabolic diseases across sites in low-income, middle-income and high-income countries. Methods The study population comprised 5916 individuals from 15 countries participating in the Burden of Obstructive Lung Disease baseline and follow-up assessments. Postbronchodilator forced expiratory volume in 1 s (FEV1), FVC and FEV1/FVC were measured at baseline. Participants who reported having doctor-diagnosed hypertension, diabetes, heart disease and stroke at follow-up but not at baseline were considered new cases of these diseases. The association between lung function and the onset of participant-reported cardiometabolic diseases was assessed in each site using regression models, and estimates were combined using random effects meta-analysis. Models were adjusted for sex, age, smoking, body mass index and educational level. Results Participants with greater per cent predicted FVC were less likely to have new-onset diabetes (OR per 10%=0.91, 95% CI 0.84 to 0.99), heart disease (OR per 10%=0.86, 95% CI 0.80 to 0.92) and stroke (OR per 10%=0.81, 95% CI 0.73 to 0.89) during the follow-up period (mean±SD 9.5±3.6 years). A greater percentage of FEV 1 was associated with a lower risk of onset of heart disease and stroke. No significant association was found between FEV 1 /FVC and onset of reported cardiometabolic diseases, except for a higher risk of diabetes (OR per 10%=1.21, 95% CI 1.08 to 1.35) in participants with higher FEV 1 /FVC. Conclusions The findings of this study suggest that a low FVC is more important than a low FEV 1 /FVC as a risk factor for developing cardiometabolic diseases. The value of including FVC in risk score models to improve their precision in predicting the onset of cardiometabolic diseases should be explored.
dc.format.extent 771477
dc.format.extent
dc.language.iso en
dc.relation.ispartofseries BMJ Open Respiratory Research; 12(1)
dc.rights info:eu-repo/semantics/openAccess
dc.subject Lungnalæknisfræði
dc.subject Clinical Epidemiology
dc.subject COPD epidemiology
dc.subject Lung Physiology
dc.subject Spirometry
dc.subject Diabetes Mellitus/epidemiology
dc.subject Humans
dc.subject Middle Aged
dc.subject Cardiovascular Diseases/epidemiology
dc.subject Risk Factors
dc.subject Male
dc.subject Forced Expiratory Volume
dc.subject Vital Capacity
dc.subject Pulmonary Disease, Chronic Obstructive/epidemiology
dc.subject Cardiometabolic Risk Factors
dc.subject Lung Diseases, Obstructive/epidemiology
dc.subject Lung/physiopathology
dc.subject Heart Diseases/epidemiology
dc.subject Female
dc.subject Adult
dc.subject Aged
dc.subject Longitudinal Studies
dc.subject Pulmonary and Respiratory Medicine
dc.title Lung function and onset of cardiometabolic diseases in the longitudinal Burden of Obstructive Lung Disease study
dc.type /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article
dc.description.version Peer reviewed
dc.identifier.doi 10.1136/bmjresp-2024-002442
dc.relation.url http://www.scopus.com/inward/record.url?scp=85215838247&partnerID=8YFLogxK
dc.contributor.department Faculty of Medicine
dc.contributor.department Other departments


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