Childhood predictors of lung function trajectories and future COPD risk: a prospective cohort study from the first to the sixth decade of life

被引:490
作者
Bui, Dinh S. [1 ]
Lodge, Caroline J. [1 ]
Burgess, John A. [1 ]
Lowe, Adrian J. [1 ]
Perret, Jennifer [1 ,3 ]
Bui, Minh Q. [1 ,2 ]
Bowatte, Gayan [1 ,4 ]
Gurrin, Lyle [1 ]
Johns, David P. [5 ]
Thompson, Bruce R. [6 ]
Hamilton, Garun S. [7 ,8 ]
Frith, Peter A. [9 ]
James, Alan L. [10 ]
Thomas, Paul S. [11 ,12 ]
Jarvis, Deborah [13 ,14 ]
Svanes, Cecilie [15 ,16 ]
Russell, Melissa [1 ]
Morrison, Stephen C. [17 ,18 ]
Feather, Iain [19 ]
Allen, Katrina J. [20 ,21 ]
Wood-Baker, Richard [5 ]
Hopper, John [1 ]
Giles, Graham G. [22 ]
Abramson, Michael J. [23 ]
Walters, Eugene H. [1 ,5 ]
Matheson, Melanie C. [1 ]
Dharmage, Shyamali C. [1 ]
机构
[1] Univ Melbourne, Sch Populat & Global Hlth, Allergy & Lung Hlth Unit, Melbourne, Vic, Australia
[2] Hanoi Univ Pharm, Dept Toxicol, Hanoi, Vietnam
[3] Inst Breathing & Sleep Heidelberg, Melbourne, Vic, Australia
[4] Natl Inst Fundamental Studies, Kandy, Sri Lanka
[5] Univ Tasmania, Dept Med, Sch Med, Hobart, Tas, Australia
[6] Alfred Hosp, Allergy Immunol & Resp Med, Melbourne, Vic, Australia
[7] Monash Hlth, Monash Lung & Sleep, Melbourne, Vic, Australia
[8] Monash Univ, Sch Clin Sci, Dept Med, Clayton, Vic, Australia
[9] Flinders Univ S Australia, Sch Med, Dept Resp Med, Adelaide, SA, Australia
[10] Sir Charles Gairdner Hosp, Dept Pulm Physiol & Sleep Med, Nedlands, WA, Australia
[11] Univ New South Wales, Prince Wales Hosp Clin Sch, Fac Med, Sydney, NSW, Australia
[12] Univ New South Wales, Sch Med Sci, Fac Med, Sydney, NSW, Australia
[13] Imperial Coll London, Dept Epidemiol & Biostat, MRC PHE Ctr Environm & Hlth, Sch Publ Hlth, London, England
[14] Imperial Coll London, Resp Epidemiol & Publ Hlth Grp, Natl Heart & Lung Inst, London, England
[15] Univ Bergen, Ctr Int Hlth, Dept Global Publ Hlth & Primary Care, Bergen, Norway
[16] Haukeland Hosp, Dept Occupat Med, Bergen, Norway
[17] Royal Brisbane & Womens Hosp, Dept Thorac Med, Brisbane, Qld, Australia
[18] Univ Queensland, Discipline Med, Brisbane, Qld, Australia
[19] Gold Coast Hosp, Dept Resp Med, Gold Coast, Qld, Australia
[20] Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[21] Univ Melbourne, Melbourne, Vic, Australia
[22] Canc Council Victoria, Canc Epidemiol Ctr, Melbourne, Vic, Australia
[23] Monash Univ, Sch Publ Hlth & Prevent Med, Dept Epidemiol & Prevent Med, Melbourne, Vic, Australia
基金
英国医学研究理事会; 欧盟地平线“2020”;
关键词
ASTHMA PHENOTYPES; REFERENCE VALUES; SMOKING; HEALTH; GROWTH; PNEUMONIA; DECLINE; BIRTH;
D O I
10.1016/S2213-2600(18)30100-0
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Background Lifetime lung function is related to quality of life and longevity. Over the lifespan, individuals follow different lung function trajectories. Identification of these trajectories, their determinants, and outcomes is important, but no study has done this beyond the fourth decade. Methods We used six waves of the Tasmanian Longitudinal Health Study (TAHS) to model lung function trajectories measured at 7,13,18,45,50, and 53 years. We analysed pre-bronchodilator FENT, z-scores at the six timepoints using group-based trajectory modelling to identify distinct subgroups of individuals whose measurements followed a similar pattern over time. We related the trajectories identified to childhood factors and risk of chronic obstructive pulmonary disease (COPD) using logistic regression, and estimated population-attributable fractions of COPD. Findings Of the 8583 participants in the original cohort, 2438 had at least two waves of lung function data at age 7 years and 53 years and comprised the study population. We identified six trajectories: early below average, accelerated decline (97 [4%] participants); persistently low (136 [6%] participants); early low, accelerated growth, normal decline (196 [8%] participants); persistently high (293 [12%] participants); below average (772 [32%] participants); and average (944 [39%] participants). The three trajectories early below average, accelerated decline; persistently low; and below average had increased risk of COPD at age 53 years compared with the average group (early below average, accelerated decline: odds ratio 35.0, 95% CI 19.5-64.0; persistently low: 9.5, 4.5-20.6; and below average: 3.7, 1.9-6.9). Early-life predictors of the three trajectories included childhood asthma, bronchitis, pneumonia, allergic rhinitis, eczema, parental asthma, and maternal smoking. Personal smoking and active adult asthma increased the impact of maternal smoking and childhood asthma, respectively, on the early below average, accelerated decline trajectory. Interpretation We identified six potential FENT, trajectories, two of which were novel. Three trajectories contributed 75% of COPD burden and were associated with modifiable early-life exposures whose impact was aggravated by adult factors. We postulate that reducing maternal smoking, encouraging immunisation, and avoiding personal smoking, especially in those with smoking parents or low childhood lung function, might minimise COPD risk. Clinicians and patients with asthma should be made aware of the potential long-term implications of non-optimal asthma control for lung function trajectory throughout life, and the role and benefit of optimal asthma control on improving lung function should be investigated in future intervention trials.
引用
收藏
页码:535 / 544
页数:10
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