Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33362
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dc.contributor.authorTan, Daniel J-
dc.contributor.authorLodge, Caroline J-
dc.contributor.authorWalters, E Haydn-
dc.contributor.authorLowe, Adrian J-
dc.contributor.authorBui, Dinh S-
dc.contributor.authorBowatte, Gayan-
dc.contributor.authorPham, Jonathan-
dc.contributor.authorErbas, Bircan-
dc.contributor.authorHui, Jennie-
dc.contributor.authorHamilton, Garun S-
dc.contributor.authorThomas, Paul S-
dc.contributor.authorHew, Mark-
dc.contributor.authorWashko, George-
dc.contributor.authorWood-Baker, Richard-
dc.contributor.authorAbramson, Michael J-
dc.contributor.authorPerret, Jennifer L-
dc.contributor.authorDharmage, Shyamali C-
dc.date.accessioned2023-07-19T02:15:46Z-
dc.date.available2023-07-19T02:15:46Z-
dc.date.issued2023-07-15-
dc.identifier.citationAmerican Journal of Respiratory and Critical Care Medicine 2023-07-15; 208(2)en_US
dc.identifier.issn1535-4970-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33362-
dc.description.abstractRationale: Asthma is a heterogeneous condition, and longitudinal phenotyping may provide new insights into the origins and outcomes of the disease. Objectives: We aimed to characterize the longitudinal phenotypes of asthma between the first and sixth decades of life in a population-based cohort study. Methods: Respiratory questionnaires were collected at seven time points in the TAHS (Tasmanian Longitudinal Health Study) when participants were aged 7, 13, 18, 32, 43, 50, and 53 years. Current-asthma and ever-asthma status was determined at each time point, and group-based trajectory modeling was used to characterize distinct longitudinal phenotypes. Linear and logistic regression models were fitted to investigate associations of the longitudinal phenotypes with childhood factors and adult outcomes. Measurements and Main Results: Of 8,583 original participants, 1,506 had reported ever asthma. Five longitudinal asthma phenotypes were identified: early-onset adolescent-remitting (40%), early-onset adult-remitting (11%), early-onset persistent (9%), late-onset remitting (13%), and late-onset persistent (27%). All phenotypes were associated with chronic obstructive pulmonary disease at age 53 years, except for late-onset remitting asthma (odds ratios: early-onset adolescent-remitting, 2.00 [95% confidence interval (CI), 1.13-3.56]; early-onset adult-remitting, 3.61 [95% CI, 1.30-10.02]; early-onset persistent, 8.73 [95% CI, 4.10-18.55]; and late-onset persistent, 6.69 [95% CI, 3.81-11.73]). Late-onset persistent asthma was associated with the greatest comorbidity at age 53 years, with increased risk of mental health disorders and cardiovascular risk factors. Conclusions: Five longitudinal asthma phenotypes were identified between the first and sixth decades of life, including two novel remitting phenotypes. We found differential effects of these phenotypes on risk of chronic obstructive pulmonary disease and nonrespiratory comorbidities in middle age.en_US
dc.language.isoeng-
dc.subjectasthma phenotypesen_US
dc.subjectchronic obstructive pulmonary diseaseen_US
dc.subjectcomorbiditiesen_US
dc.subjectlongitudinal phenotypesen_US
dc.subjecttrajectoriesen_US
dc.titleLongitudinal Asthma Phenotypes from Childhood to Middle-Age: A Population-based Cohort Study.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAmerican Journal of Respiratory and Critical Care Medicineen_US
dc.identifier.affiliationAllergy and Lung Health Unit, School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationSchool of Medicine, University of Tasmania, Hobart, Tasmania, Australia.en_US
dc.identifier.affiliationDepartment of Basic Sciences, Faculty of Allied Health Sciences, University of Peradeniya, Peradeniya, Sri Lanka.en_US
dc.identifier.affiliationAllergy, Asthma and Clinical Immunology, The Alfred Hospital, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationSchool of Psychology and Public Health, La Trobe University, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationSchool of Population and Global Health, University of Western Australia, Perth, Western Australia, Australia.en_US
dc.identifier.affiliationMonash Lung, Sleep, Allergy & Immunology, Monash Health, Melbourne, Victoria, Australia.;School of Clinical Sciences and.en_US
dc.identifier.affiliationPrince of Wales Clinical School, Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia.en_US
dc.identifier.affiliationDepartment of Basic Sciences, Faculty of Allied Health Sciences, University of Peradeniya, Peradeniya, Sri Lanka.;School of Public Health & Preventive Medicine, Monash University, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationDivision of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, Massachusetts; and.en_US
dc.identifier.affiliationSchool of Medicine, University of Tasmania, Hobart, Tasmania, Australia.en_US
dc.identifier.affiliationPrince of Wales Clinical School, Faculty of Medicine, University of New South Wales, Sydney, New South Wales, Australia.en_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.doi10.1164/rccm.202208-1569OCen_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-3536-8756en_US
dc.identifier.orcid0000-0002-4388-784Xen_US
dc.identifier.orcid0000-0001-7034-0615en_US
dc.identifier.pubmedid37209134-
dc.description.volume208-
dc.description.issue2-
dc.description.startpage132-
dc.description.endpage141-
dc.subject.meshtermssecondaryAsthma/genetics-
local.name.researcherPerret, Jennifer L
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptInstitute for Breathing and Sleep-
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