TY - JOUR
T1 - Characterisation of lung function trajectories and associated early-life predictors in an Australian birth cohort study
AU - Sanna, Francesca
AU - Locatelli, Francesca
AU - Sly, Peter D.
AU - White, Elisha
AU - Heyworth, Jane
AU - Hall, Graham L.
AU - Foong, Rachel E.
AU - Blake, David
N1 - Funding Information:
Acknowledgements: We would like to acknowledge the Raine Study participants and their families for their ongoing participation in the study, and the Raine Study team for study coordination and data collection. We also thank the National Health and Medical Research Council (NHMRC) for their long-term contribution to funding the study over the last 30 years. The core management of the Raine Study is funded by The University of Western Australia, Curtin University, Telethon Kids Institute, Women and Infants Research Foundation, Edith Cowan University, Murdoch University, The University of Notre Dame Australia and the Raine Medical Research Foundation. The Raine Study Gen2 14-year follow-up was funded by NHMRC project grant 211192, NMHRC Program Grant 003209 and the Raine Medical Research Foundation. The Raine Study Gen2-22 year follow-up was funded by NHMRC project grants 1027449, 1044840 and 1021858. We further acknowledge Jackie Joseph Bowen for the contribution on the sixth-year lung function measurements, and Marie Deverall and Lisha Van Reyk for the 14th year lung function measurements.
Funding Information:
We would like to acknowledge the Raine Study participants and their families for their ongoing participation in the study, and the Raine Study team for study coordination and data collection. We also thank the National Health and Medical Research Council (NHMRC) for their long-term contribution to funding the study over the last 30 years. The core management of the Raine Study is funded by The University of Western Australia, Curtin University, Telethon Kids Institute, Women and Infants Research Foundation, Edith Cowan University, Murdoch University, The University of Notre Dame Australia and the Raine Medical Research Foundation. The Raine Study Gen2 14-year follow-up was funded by NHMRC project grant 211192, NMHRC Program Grant 003209 and the Raine Medical Research Foundation. The Raine Study Gen2-22 year follow-up was funded by NHMRC project grants 1027449, 1044840 and 1021858. We further acknowledge Jackie Joseph Bowen for the contribution on the sixth-year lung function measurements, and Marie Deverall and Lisha Van Reyk for the 14th year lung function measurements.
Publisher Copyright:
© The authors 2022.
PY - 2022/2/14
Y1 - 2022/2/14
N2 - Background There is growing evidence that lung function in early-life predicts later lung function. Adverse events over the lifespan might influence an individual’s lung function trajectory, resulting in poor respiratory health. The aim of this study is to identify early-life risk factors and their impact on lung function trajectories to prevent long-term lung impairments. Methods Our study included participants from the Raine Study, a prospective pregnancy cohort, with at least two spirometry measurements. Lung function trajectories from the 6-to 22-year follow-ups were characterised using finite mixture modelling. Multinomial logistic regression analyses were used to evaluate the association between early-life predictors and lung function trajectories. Main results A total of 1512 participants (768 males, 744 females), representing 53% of the whole cohort, were included in this analysis. Four lung function trajectories of forced expiratory volume in 1 s (FEV1 ), forced vital capacity (FVC) and FEV1/FVC (z-scores) were identified. FEV1 and FVC trajectories were categorised as: “very low”, “low”, “average” and “above average”, respectively. Based on their shape, lung function trajectories of FEV1/FVC were categorised as “very low”, “low–average”, “average–low” and “average”. Asthma and maternal smoking were identified as risk factors for low lung function trajectories in this cohort, as well as early-life exposure to PM2.5Absorbance . Conclusions Early-life risk factors may influence lung function trajectories over time. Nonetheless, identifying children with a high risk of having low lung function trajectories should be prioritised to prevent deficits in later life.
AB - Background There is growing evidence that lung function in early-life predicts later lung function. Adverse events over the lifespan might influence an individual’s lung function trajectory, resulting in poor respiratory health. The aim of this study is to identify early-life risk factors and their impact on lung function trajectories to prevent long-term lung impairments. Methods Our study included participants from the Raine Study, a prospective pregnancy cohort, with at least two spirometry measurements. Lung function trajectories from the 6-to 22-year follow-ups were characterised using finite mixture modelling. Multinomial logistic regression analyses were used to evaluate the association between early-life predictors and lung function trajectories. Main results A total of 1512 participants (768 males, 744 females), representing 53% of the whole cohort, were included in this analysis. Four lung function trajectories of forced expiratory volume in 1 s (FEV1 ), forced vital capacity (FVC) and FEV1/FVC (z-scores) were identified. FEV1 and FVC trajectories were categorised as: “very low”, “low”, “average” and “above average”, respectively. Based on their shape, lung function trajectories of FEV1/FVC were categorised as “very low”, “low–average”, “average–low” and “average”. Asthma and maternal smoking were identified as risk factors for low lung function trajectories in this cohort, as well as early-life exposure to PM2.5Absorbance . Conclusions Early-life risk factors may influence lung function trajectories over time. Nonetheless, identifying children with a high risk of having low lung function trajectories should be prioritised to prevent deficits in later life.
UR - http://www.scopus.com/inward/record.url?scp=85127715427&partnerID=8YFLogxK
U2 - 10.1183/23120541.00072-2022
DO - 10.1183/23120541.00072-2022
M3 - Article
C2 - 35350282
AN - SCOPUS:85127715427
SN - 2312-0541
VL - 8
JO - ERJ Open Research
JF - ERJ Open Research
IS - 1
M1 - 00072-2022
ER -