Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/17274
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dc.contributor.authorPerret, Jennifer L-
dc.contributor.authorMatheson, Melanie C-
dc.contributor.authorGurrin, Lyle C-
dc.contributor.authorJohns, David P-
dc.contributor.authorBurgess, John A-
dc.contributor.authorThompson, Bruce R-
dc.contributor.authorLowe, Adrian J-
dc.contributor.authorMarkos, James-
dc.contributor.authorMorrison, Stephen S-
dc.contributor.authorMcDonald, Christine F-
dc.contributor.authorWood-Baker, Richard-
dc.contributor.authorSvanes, Cecilie-
dc.contributor.authorThomas, Paul S-
dc.contributor.authorHopper, John L-
dc.contributor.authorGiles, Graham G-
dc.contributor.authorAbramson, Michael J-
dc.contributor.authorWalters, E Haydn-
dc.contributor.authorDharmage, Shyamali C-
dc.date2018-03-20-
dc.date.accessioned2018-03-22T23:32:11Z-
dc.date.available2018-03-22T23:32:11Z-
dc.date.issued2018-03-20-
dc.identifier.citationRespirology 2018; 23(8): 780-787en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/17274-
dc.description.abstractChronic obstructive pulmonary disease (COPD) has potential origins in childhood but an association between childhood measles and post-bronchodilator (BD) airflow obstruction (AO) has not yet been shown. We investigated whether childhood measles contributed to post-BD AO through interactions with asthma and/or smoking in a non-immunized middle-aged population. The population-based Tasmanian Longitudinal Health Study (TAHS) cohort born in 1961 (n = 8583) underwent spirometry in 1968 before immunization was introduced. A history of childhood measles infection was obtained from school medical records. During the fifth decade follow-up (n = 5729 responses), a subgroup underwent further lung function measurements (n = 1389). Relevant main associations and interactions by asthma and/or smoking on post-BD forced expiratory volume in 1 s/forced vital capacity (FEV1/FVC; continuous variable) and AO (FEV1/FVC < lower limit of normal) were estimated by multiple regression. Sixty-nine percent (n = 950) had a history of childhood measles. Childhood measles augmented the combined adverse effect of current clinical asthma and smoking at least 10 pack-years on post-BD FEV1/FVC ratio in middle age (z-score: -0.70 (95% CI: -1.1 to -0.3) vs -1.36 (-1.6 to -1.1), three-way interaction: P = 0.009), especially for those with childhood-onset asthma. For never- and ever-smokers of <10 pack-years who had current asthma symptoms, compared with those without childhood measles, paradoxically, the odds for post-BD AO was not significant in the presence of childhood measles (OR: 12.0 (95% CI: 3.4-42) vs 2.17 (0.9-5.3)). Childhood measles infection appears to compound the associations between smoking, current asthma and post-BD AO. Differences between asthma subgroups provide further insight into the complex aetiology of obstructive lung diseases for middle-aged adults.en_US
dc.language.isoeng-
dc.subjectasthma-COPD overlapen_US
dc.subjectchildhood measlesen_US
dc.subjectcurrent adult asthmaen_US
dc.subjectinteractionen_US
dc.subjectsmokingen_US
dc.titleChildhood measles contributes to post-bronchodilator airflow obstruction in middle-aged adults: A cohort study.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleRespirologyen_US
dc.identifier.affiliationLaunceston General Hospital, Hobart, TAS, Australiaen_US
dc.identifier.affiliationAllergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, The University of Melbourne, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationCentre for International Health, University of Bergen, Bergen, Norwayen_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_US
dc.identifier.affiliationDepartment of Occupational Medicine, Haukelaud University Hospital, Bergen, Norwayen_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliation"Breathe Well" Centre of Research Excellence for Chronic Respiratory Disease and Lung Ageing, School of Medicine, University of Tasmania, Hobart, TAS, Australiaen_US
dc.identifier.affiliationDepartment of Allergy, Immunology and Respiratory Medicine, The Alfred Hospital, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, Monash University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, University of Queensland, Brisbane, QLD, Australiaen_US
dc.identifier.affiliationPrince of Wales' Hospital Clinical School and School of Medical Sciences, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australiaen_US
dc.identifier.affiliationDepartment of Public Health, Seoul National University, Seoul, Republic of Koreaen_US
dc.identifier.affiliationCancer Epidemiology & Intelligence Division, Cancer Council Victoria, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australiaen_US
dc.identifier.doi10.1111/resp.13297en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-7034-0615en_US
dc.identifier.orcid0000-0002-1575-6850en_US
dc.identifier.orcid0000-0001-6481-3391en_US
dc.identifier.orcid0000-0002-9954-0538en_US
dc.identifier.pubmedid29560611-
dc.type.austinJournal Article-
local.name.researcherMcDonald, Christine F
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
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