Impact of lifetime body mass index trajectories on the incidence and persistence of adult asthma.


Journal

The European respiratory journal
ISSN: 1399-3003
Titre abrégé: Eur Respir J
Pays: England
ID NLM: 8803460

Informations de publication

Date de publication:
09 2022
Historique:
received: 19 08 2021
accepted: 30 01 2022
pubmed: 26 2 2022
medline: 20 9 2022
entrez: 25 2 2022
Statut: epublish

Résumé

High body mass index (BMI) trajectories from childhood to adulthood are associated with the development of some chronic diseases, but whether such trajectories influence adult asthma has not been investigated to date. Therefore, we investigated associations between BMI trajectories from childhood to middle age (5-43 years) and incidence, persistence and relapse of asthma from ages 43 to 53 years. In the Tasmanian Longitudinal Health Study (n=4194), weight and height were recorded at eight time-points between 5 and 43 years of age. BMI trajectories were developed using group-based trajectory modelling. Associations between BMI trajectories and asthma incidence, persistence and relapse from age 43 to 53 years, bronchial hyperresponsiveness (BHR) at age 50 years, and bronchodilator responsiveness at age 53 years were modelled using multiple logistic and linear regression. Five distinct BMI trajectories were identified: average, low, child high-decreasing, child average-increasing and high. Compared with the average trajectory, child average-increasing and high trajectories were associated with increased risk of incident asthma (OR 2.6, 95% CI 1.1-6.6 and OR 4.4, 95% CI 1.7-11.4, respectively) and BHR in middle age (OR 2.9, 95% CI 1.1-7.5 and OR 3.5, 95% CI 1.1-11.4, respectively). No associations were observed for asthma persistence or relapse. Participants with child average-increasing and high BMI trajectories from childhood to middle age were at higher risk of incident adult asthma. Thus, encouraging individuals to maintain a normal BMI over the life course may help reduce the burden of adult asthma.

Sections du résumé

BACKGROUND
High body mass index (BMI) trajectories from childhood to adulthood are associated with the development of some chronic diseases, but whether such trajectories influence adult asthma has not been investigated to date. Therefore, we investigated associations between BMI trajectories from childhood to middle age (5-43 years) and incidence, persistence and relapse of asthma from ages 43 to 53 years.
METHODS
In the Tasmanian Longitudinal Health Study (n=4194), weight and height were recorded at eight time-points between 5 and 43 years of age. BMI trajectories were developed using group-based trajectory modelling. Associations between BMI trajectories and asthma incidence, persistence and relapse from age 43 to 53 years, bronchial hyperresponsiveness (BHR) at age 50 years, and bronchodilator responsiveness at age 53 years were modelled using multiple logistic and linear regression.
RESULTS
Five distinct BMI trajectories were identified: average, low, child high-decreasing, child average-increasing and high. Compared with the average trajectory, child average-increasing and high trajectories were associated with increased risk of incident asthma (OR 2.6, 95% CI 1.1-6.6 and OR 4.4, 95% CI 1.7-11.4, respectively) and BHR in middle age (OR 2.9, 95% CI 1.1-7.5 and OR 3.5, 95% CI 1.1-11.4, respectively). No associations were observed for asthma persistence or relapse.
CONCLUSIONS
Participants with child average-increasing and high BMI trajectories from childhood to middle age were at higher risk of incident adult asthma. Thus, encouraging individuals to maintain a normal BMI over the life course may help reduce the burden of adult asthma.

Identifiants

pubmed: 35210325
pii: 13993003.02286-2021
doi: 10.1183/13993003.02286-2021
pii:
doi:

Substances chimiques

Bronchodilator Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright ©The authors 2022. For reproduction rights and permissions contact permissions@ersnet.org.

Déclaration de conflit d'intérêts

Conflicts of interest: M.J. Abramson holds investigator-initiated grants for unrelated research from Pfizer, Boehringer Ingelheim and Sanofi; has undertaken an unrelated consultancy for and received assistance with conference attendance from Sanofi; and has also received a speaker's fee from GSK. The other authors included in this study declare that they have no competing interests. All authors declare no support from any organisation or no financial relationship with any organisation that could appear to have influenced the submitted work.

Auteurs

Gulshan Bano Ali (GB)

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Australia.

Adrian J Lowe (AJ)

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Australia.
Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia.

Jennifer L Perret (JL)

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Australia.
Institute for Breathing and Sleep (IBAS), Melbourne, Australia.

E Haydn Walters (EH)

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Australia.
School of Medicine, University of Tasmania, Hobart, Australia.

Caroline J Lodge (CJ)

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Australia.

David Johns (D)

School of Medicine, University of Tasmania, Hobart, Australia.

Alan James (A)

Dept of Pulmonary Physiology and Sleep Medicine, Sir Charles Gairdner Hospital, Nedlands, Australia.
Medical School, University of Western Australia, Perth, Australia.

Bircan Erbas (B)

School of Psychology and Public Health, La Trobe University, Melbourne, Australia.

Garun S Hamilton (GS)

Dept of Lung and Sleep, Sleep Medicine Research at Monash Medical Centre, Clayton, Australia.
School of Clinical Sciences, Monash University, Clayton, Australia.

Gayan Bowatte (G)

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Australia.

Richard Wood-Baker (R)

School of Medicine, University of Tasmania, Hobart, Australia.

Michael J Abramson (MJ)

School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.

Dinh S Bui (DS)

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Australia.
D.S. Bui and S.C. Dharmage are equal senior authors.

Shyamali C Dharmage (SC)

Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Australia s.dharmage@unimelb.edu.au.
Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia.
D.S. Bui and S.C. Dharmage are equal senior authors.

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Classifications MeSH