Open Access Research article

The role of ALOX5AP, LTA4H and LTB4R polymorphisms in determining baseline lung function and COPD susceptibility in UK smokers

Asif S Tulah1, Stuart G Parker2, Miriam F Moffatt3, Andrew J Wardlaw4, Martin J Connolly5 and Ian Sayers1*

1 Division of Therapeutics and Molecular Medicine, Nottingham Respiratory Biomedical Research Unit, University of Nottingham, Queen's Medical Centre, Nottingham, UK

2 Sheffield Institute for Studies on Ageing, University of Sheffield, Barnsley Hospital NHSFT, Barnsley, UK

3 National Heart and Lung Institute, Imperial College London, London, UK

4 Institute for Lung Health and Department of Infection, Immunity and Inflammation, Glenfield Hospital, University of Leicester, Leicester, UK

5 Freemasons' Department of Geriatric Medicine, University of Auckland, Auckland

For all author emails, please log on.

BMC Medical Genetics 2011, 12:173 doi:10.1186/1471-2350-12-173

Published: 29 December 2011

Additional files

Additional file 1:

Baseline lung function (FEV1 and FEV1/FVC ratio) and ALOX5AP, LTA4H and LTB4R SNPs in the smokers (n = 992). This table shows the results of the association analysis between leukotriene pathway SNPs and baseline FEV1 and FEV1/FVC using the additive model. Covariates included in the model were age, gender, height and pack years. Associations with p < 0.05 are shown in bold black.

Format: DOC Size: 70KB Download file

This file can be viewed with: Microsoft Word Viewer

Open Data