Research Paper Volume 12, Issue 1 pp 518—542
Association of adult lung function with accelerated biological aging
- 1 Human Development and Health, Faculty of Medicine, University of Southampton, Southampton, United Kingdom
- 2 Chronic Disease Epidemiology Unit, Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, Switzerland
- 3 University of Basel, Basel, Switzerland
- 4 Population Health and Occupational Disease, NHLI, Imperial College London, London, United Kingdom
- 5 MRC-PHE Centre for Environment and Health, Imperial College London, London, United Kingdom
- 6 Department of Epidemiology and Biostatistics, MRC–PHE Centre for Environment and Health, School of Public Health, Imperial College London, London, United Kingdom
- 7 Department of Clinical Science, University of Bergen, Bergen, Norway
- 8 Department of Gynecology and Obstetrics, University of Bergen, Bergen, Norway
received: July 8, 2019 ; accepted: December 23, 2019 ; published: January 11, 2020 ;https://doi.org/10.18632/aging.102639
How to Cite
Copyright © 2020 Rezwan et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Lung function, strongly associated with morbidity and mortality, decreases with age. This study examines whether poor adult lung function is associated with age accelerations (AAs). DNA methylation (DNAm) based AAs, lifespan predictors (GrimAge and plasminogen activator inhibitor 1-PAI1) and their related age-adjusted measures were estimated from peripheral blood at two time points (8-to-11 years apart) in adults from two cohorts: SAPALDIA (n=987) and ECRHS (n=509). Within each cohort and stratified by gender (except for estimators from GrimAge and PAI1), AAs were used as predictors in multivariate linear regression with cross-sectional lung function parameters, and in covariate-adjusted mixed linear regression with longitudinal change in lung function and meta-analysed.
AAs were found cross-sectionally associated with lower mean FEV1 (Forced Expiratory Volume in one second) (AA-residuals:P-value=4x10-4; Intrinsic Epigenetic AA:P-value=2x10-4) in females at the follow-up time point only, and the same trend was observed for FVC (Forced Vital Capacity). Both lifespan and plasma level predictors were observed strongly associated with lung function decline and the decline was stronger in the follow-up time points (strongest association between FEV1 and DNAmAge GrimAge:P-value=1.25x10-17).
This study suggests that DNAm based lifespan and plasma level predictors can be utilised as important factors to assess lung health in adults.