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Genetic variants affecting cross-sectional lung function in adults show little or no effect on longitudinal lung function decline

John, Catherine; Soler Artigas, Mar�a; Hui, Jennie; Nielsen, Sune Fallgaard; Rafaels, Nicholas; Par�, Peter D; Hansel, Nadia N.; Shrine, Nick; Kilty, Iain; Malarstig, Anders; Jelinsky, Scott A; Vedel-Krogh, Signe; Barnes, Kathleen; Hall, Ian P.; Beilby, John; Musk, Arthur W.; Nordestgaard, B�rge G.; James, Alan; Wain, Louise V.; Tobin, Martin D.

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Authors

Catherine John

Mar�a Soler Artigas

Jennie Hui

Sune Fallgaard Nielsen

Nicholas Rafaels

Peter D Par�

Nadia N. Hansel

Nick Shrine

Iain Kilty

Anders Malarstig

Scott A Jelinsky

Signe Vedel-Krogh

Kathleen Barnes

Ian P. Hall

John Beilby

Arthur W. Musk

B�rge G. Nordestgaard

Alan James

Louise V. Wain

Martin D. Tobin



Abstract

Background: Genome-wide association studies have identified numerous genetic regions that influence cross-sectional lung function. Longitudinal decline in lung function also includes a heritable component but the genetic determinants have yet to be defined.
Objectives: We aimed to determine whether regions associated with cross-sectional lung function were also associated with longitudinal decline and to seek novel variants which influence decline.
Methods: We analysed genome-wide data from 4167 individuals from the Busselton Health Study cohort, who had undergone spirometry (12 695 observations across eight time points). A mixed model was fitted and weighted risk scores were calculated for the joint effect of 26 known regions on baseline and longitudinal changes in FEV1 and FEV1/FVC. Potential additional regions of interest were identified and followed up in two independent cohorts.
Results: The 26 regions previously associated with cross-sectional lung function jointly showed a strong effect on baseline lung function (p=4.44×10−16 for FEV1/FVC) but no effect on longitudinal decline (p=0.160 for FEV1/FVC). This was replicated in an independent cohort. 39 additional regions of interest (48 variants) were identified; these associations were not replicated in two further cohorts.
Conclusions: Previously identified genetic variants jointly have a strong effect on cross-sectional lung function in adults but little or no effect on the rate of decline of lung function. It is possible that they influence COPD risk through lung development. Although no genetic variants have yet been associated with lung function decline at stringent genome-wide significance, longitudinal change in lung function is heritable suggesting that there is scope for future discoveries.

Citation

John, C., Soler Artigas, M., Hui, J., Nielsen, S. F., Rafaels, N., Paré, P. D., Hansel, N. N., Shrine, N., Kilty, I., Malarstig, A., Jelinsky, S. A., Vedel-Krogh, S., Barnes, K., Hall, I. P., Beilby, J., Musk, A. W., Nordestgaard, B. G., James, A., Wain, L. V., & Tobin, M. D. (2017). Genetic variants affecting cross-sectional lung function in adults show little or no effect on longitudinal lung function decline. Thorax, 72(5), https://doi.org/10.1136/thoraxjnl-2016-208448

Journal Article Type Article
Acceptance Date Nov 25, 2016
Online Publication Date Feb 7, 2017
Publication Date May 1, 2017
Deposit Date Jul 20, 2017
Publicly Available Date Jul 20, 2017
Journal Thorax
Print ISSN 0040-6376
Electronic ISSN 1468-3296
Publisher BMJ Publishing Group
Peer Reviewed Peer Reviewed
Volume 72
Issue 5
DOI https://doi.org/10.1136/thoraxjnl-2016-208448
Public URL https://nottingham-repository.worktribe.com/output/858725
Publisher URL http://thorax.bmj.com/content/72/5/400
Contract Date Jul 20, 2017