Distinctive lung function trajectories from age 10 to 26 years in men and women and associated early life risk factors – a birth cohort study

Abstract Pre-bronchodilator lung function including forced vital capacity (FVC), forced expiratory flow in 1 second (FEV1), their ratio (FEV1/FVC), and forced expiratory flow 25–75% (FEF25–75) measured at age 10, 18, and 26 years in the Isle of Wight birth cohort was analyzed for developmental patte...

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Main Authors: Wilfried Karmaus, Nandini Mukherjee, Vimala Devi Janjanam, Su Chen, Hongmei Zhang, Graham Roberts, Ramesh J. Kurukulaaratchy, Hasan Arshad
Format: Article
Language:English
Published: BMC 2019-05-01
Series:Respiratory Research
Online Access:http://link.springer.com/article/10.1186/s12931-019-1068-0
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spelling doaj-a4cba0afa76f42f2ae11cc6db942cda32020-11-25T02:57:39ZengBMCRespiratory Research1465-993X2019-05-0120111310.1186/s12931-019-1068-0Distinctive lung function trajectories from age 10 to 26 years in men and women and associated early life risk factors – a birth cohort studyWilfried Karmaus0Nandini Mukherjee1Vimala Devi Janjanam2Su Chen3Hongmei Zhang4Graham Roberts5Ramesh J. Kurukulaaratchy6Hasan Arshad7Division of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, University of MemphisDivision of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, University of MemphisDivision of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, University of MemphisDepartment of Mathematical Sciences, The University of MemphisDivision of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, University of MemphisPaediatric Allergy and Respiratory Medicine, Faculty of Medicine, University of SouthamptonClinical and Experimental Sciences, Faculty of Medicine, University of SouthamptonClinical and Experimental Sciences, Faculty of Medicine, University of SouthamptonAbstract Pre-bronchodilator lung function including forced vital capacity (FVC), forced expiratory flow in 1 second (FEV1), their ratio (FEV1/FVC), and forced expiratory flow 25–75% (FEF25–75) measured at age 10, 18, and 26 years in the Isle of Wight birth cohort was analyzed for developmental patterns (trajectories). Early life risk factors before the age of 10 years were assessed for the trajectories. Method Members of the birth cohort (1989/90) were followed at age 1, 2, 4, 10, 18, and 26 years. Allergic sensitization and questionnaire data were collected. Spirometry tests were performed and evaluated according to the American Thoracic Society (ATS) criteria at 10, 18, and 26 years. To identify developmental trajectories for FVC, FEV1, FEV1/FVC, and FEF25–75 from 10 to 26 years, a finite mixture model was applied to the longitudinal lung function data, separately for males and females. Associations of early life factors with the respective lung function trajectories were assessed using log-linear and logistic regression analyses. Results Both high and low lung function trajectories were observed in men and women. FVC continued to grow beyond 18 years in men and women, whereas FEV1 peaked at age 18 years in female trajectories and in one male trajectory. For the FEV1/FVC ratios and FEF25–75 most trajectories appeared highest at age 18 and declined thereafter. However, the low FEV1/FVC trajectory in both sexes showed an early decline at 10 years. Lower birth weight was linked with lower lung function trajectories in males and females. Eczema in the first year of life was a risk factor for later lung function deficits in females, whereas the occurrence of asthma at 4 years of age was a risk factor for later lung function deficits in males. A positive skin prick test at age four was a risk for the low FEV1 trajectory in females and for the low FEV1/FVC trajectory in males. Conclusion Men and women showed distinctive lung function trajectories and associated risk factors. Lower lung function trajectories can be explained by not achieving maximally attainable function at age 18 years and by a function decline from 18 to 26 years.http://link.springer.com/article/10.1186/s12931-019-1068-0
collection DOAJ
language English
format Article
sources DOAJ
author Wilfried Karmaus
Nandini Mukherjee
Vimala Devi Janjanam
Su Chen
Hongmei Zhang
Graham Roberts
Ramesh J. Kurukulaaratchy
Hasan Arshad
spellingShingle Wilfried Karmaus
Nandini Mukherjee
Vimala Devi Janjanam
Su Chen
Hongmei Zhang
Graham Roberts
Ramesh J. Kurukulaaratchy
Hasan Arshad
Distinctive lung function trajectories from age 10 to 26 years in men and women and associated early life risk factors – a birth cohort study
Respiratory Research
author_facet Wilfried Karmaus
Nandini Mukherjee
Vimala Devi Janjanam
Su Chen
Hongmei Zhang
Graham Roberts
Ramesh J. Kurukulaaratchy
Hasan Arshad
author_sort Wilfried Karmaus
title Distinctive lung function trajectories from age 10 to 26 years in men and women and associated early life risk factors – a birth cohort study
title_short Distinctive lung function trajectories from age 10 to 26 years in men and women and associated early life risk factors – a birth cohort study
title_full Distinctive lung function trajectories from age 10 to 26 years in men and women and associated early life risk factors – a birth cohort study
title_fullStr Distinctive lung function trajectories from age 10 to 26 years in men and women and associated early life risk factors – a birth cohort study
title_full_unstemmed Distinctive lung function trajectories from age 10 to 26 years in men and women and associated early life risk factors – a birth cohort study
title_sort distinctive lung function trajectories from age 10 to 26 years in men and women and associated early life risk factors – a birth cohort study
publisher BMC
series Respiratory Research
issn 1465-993X
publishDate 2019-05-01
description Abstract Pre-bronchodilator lung function including forced vital capacity (FVC), forced expiratory flow in 1 second (FEV1), their ratio (FEV1/FVC), and forced expiratory flow 25–75% (FEF25–75) measured at age 10, 18, and 26 years in the Isle of Wight birth cohort was analyzed for developmental patterns (trajectories). Early life risk factors before the age of 10 years were assessed for the trajectories. Method Members of the birth cohort (1989/90) were followed at age 1, 2, 4, 10, 18, and 26 years. Allergic sensitization and questionnaire data were collected. Spirometry tests were performed and evaluated according to the American Thoracic Society (ATS) criteria at 10, 18, and 26 years. To identify developmental trajectories for FVC, FEV1, FEV1/FVC, and FEF25–75 from 10 to 26 years, a finite mixture model was applied to the longitudinal lung function data, separately for males and females. Associations of early life factors with the respective lung function trajectories were assessed using log-linear and logistic regression analyses. Results Both high and low lung function trajectories were observed in men and women. FVC continued to grow beyond 18 years in men and women, whereas FEV1 peaked at age 18 years in female trajectories and in one male trajectory. For the FEV1/FVC ratios and FEF25–75 most trajectories appeared highest at age 18 and declined thereafter. However, the low FEV1/FVC trajectory in both sexes showed an early decline at 10 years. Lower birth weight was linked with lower lung function trajectories in males and females. Eczema in the first year of life was a risk factor for later lung function deficits in females, whereas the occurrence of asthma at 4 years of age was a risk factor for later lung function deficits in males. A positive skin prick test at age four was a risk for the low FEV1 trajectory in females and for the low FEV1/FVC trajectory in males. Conclusion Men and women showed distinctive lung function trajectories and associated risk factors. Lower lung function trajectories can be explained by not achieving maximally attainable function at age 18 years and by a function decline from 18 to 26 years.
url http://link.springer.com/article/10.1186/s12931-019-1068-0
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