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Title: | Associations between life-course FEV1/FVC trajectories and respiratory symptoms up to middle age: analysis of data from two prospective cohort studies. | Austin Authors: | Perret, Jennifer L ;Bui, Dinh S;Pistenmaa, Carrie;Vicendese, Don;Khan, Sadiya S;Han, MeiLan K;San José Estépar, Raul;Lowe, Adrian J;Lodge, Caroline J;Labaki, Wassim W;Pham, Jonathan V;Idrose, Nur Sabrina;Senaratna, Chamara V;Tan, Daniel J;Hamilton, Garun S;Thompson, Bruce R;Munsif, Maitri;Arynchyn, Alexander;Jacobs, David R;Abramson, Michael J;Walters, E Haydn;Washko, George R;Kalhan, Ravi;Dharmage, Shyamali C | Affiliation: | Institute for Breathing and Sleep Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia. Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, MA, USA. Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia; School of Computing, Engineering and Mathematical Sciences, La Trobe University, Bundoora, VIC, Australia. Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. Division of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor, MI, USA. Department of Radiology, Brigham and Women's Hospital, Boston, MA, USA. Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia; Murdoch Childrens Research Institute, Parkville, VIC, Australia. Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia; Murdoch Childrens Research Institute, Parkville, VIC, Australia. Division of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor, MI, USA. Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia; Asthma, Allergy and Clinical Immunology (AACI) service, Department of Respiratory Medicine, Alfred Health, Melbourne, VIC, Australia. Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia. Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia. Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia. Monash Lung, Sleep, Allergy and Immunology, Monash Health, Melbourne, VIC, Australia; School of Clinical Sciences, Monash University, Melbourne, VIC, Australia. Melbourne School of Health Science, The University of Melbourne, Melbourne, VIC, Australia. Department of Respiratory and Sleep Medicine, Austin Hospital, Melbourne, VIC, Australia; Institute for Breathing and Sleep (IBAS), Melbourne, VIC, Australia. School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA. School of Public Health, University of Minnesota, Minneapolis, MN, USA. School of Public Health & Preventive Medicine, Monash University, Melbourne, VIC, Australia. Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia; School of Medicine, University of Tasmania, Hobart, TAS, Australia. Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, MA, USA. Division of Pulmonary and Critical Care Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. Allergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia; Murdoch Childrens Research Institute, Parkville, VIC, Australia. |
Issue Date: | 27-Nov-2024 | Date: | 2024 | Publication information: | The Lancet. Respiratory Medicine 2024-11-27 | Abstract: | Life-course lung function trajectories leading to airflow obstruction, as measured by impaired FEV1/FVC (forced vital capacity), precede the onset of chronic obstructive pulmonary disease (COPD). We aimed to investigate whether individuals on impaired FEV1/FVC trajectories have an increased burden of respiratory symptoms, including those who do not meet the spirometric criteria for COPD. We analysed serial life-course data from two population-based cohort studies separately, which included respiratory symptoms and spirometry: the Tasmanian Longitudinal Health Study (TAHS, Australia) cohort was recruited at age 6-7 years and followed up until middle age (mean age 53 years; range 51-55); and the Coronary Artery Risk Development in Young Adults (CARDIA, USA) cohort was recruited at a mean age of 25 years (range 18-30) and followed up to a mean age of 55 years (range 47-64). Participants' symptom profiles at ages 53 and 55 years were derived by latent class analysis. Symptom profiles were compared across pre-bronchodilator FEV1/FVC trajectories derived by group-based modelling, then restricted to those without COPD defined by post-bronchodilator airflow obstruction (FEV1/FVC <5th percentile) at ages 51-55 years and 47-64 years. Six FEV1/FVC trajectories previously derived for TAHS were replicated in CARDIA. Optimal models identified five symptom profiles in TAHS (n=2421) and six in CARDIA (n=3153). For both cohorts, the most impaired FEV1/FVC trajectory (early low, rapid decline in TAHS; low peak, rapid decline in CARDIA) was associated with predominant wheeze (multinomial odds ratio [mOR] 6·71 [95% CI 4·10-10·90] in TAHS and 9·90 [4·52-21·70] in CARDIA) and nearly all respiratory symptoms (4·95 [2·52-9·74] and 14·80 [5·97-36·60]) at age 51-55 years in TAHS and age 47-64 years in CARDIA, compared with the average trajectory. Among individuals belonging to the three most impaired trajectories, the associations with predominant wheeze increased with worsening FEV1/FVC impairment and persisted when considering only those without spirometry-defined COPD. Additionally, for those belonging to the two rapid decline trajectories, both wheezing and usual phlegm or bronchitis were reported by 54 (20%) of 265 participants younger than 14 years in TAHS and by 31 (25%) of 123 participants aged 30 years or younger in CARDIA. In two independent cohorts that collected similar data, people on impaired FEV1/FVC trajectories often had a longstanding history of both wheeze and phlegm or bronchitis, and wheeze was the predominant symptom in individuals aged 47-64 years among those who had not already progressed to COPD. National Health and Medical Research Council (Australia); The University of Melbourne; Clifford Craig Medical Research Trust; Victorian, Queensland & Tasmanian Asthma Foundations; Royal Hobart Hospital Research Foundation; Helen MacPherson Smith Trust; GlaxoSmithKline; National Heart, Lung, and Blood Institute of the US National Institutes of Health. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/35607 | DOI: | 10.1016/S2213-2600(24)00265-0 | ORCID: | Journal: | The Lancet. Respiratory Medicine | PubMed URL: | 39615504 | ISSN: | 2213-2619 | Type: | Journal Article |
Appears in Collections: | Journal articles |
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