Variants in the 15q24/25 locus associate with lung function decline in active smokers.

Genetic variation in nicotinic acetylcholine receptor subunit genes (nAChRs) is associated with lung function level and chronic obstructive pulmonary disease (COPD). It is unknown whether these variants also predispose to an accelerated lung function decline. We investigated the association of nAChR...

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Main Authors: Firdaus A A Mohamed Hoesein, Els Wauters, Wim Janssens, Harry J M Groen, Joanna Smolonska, Cisca Wijmenga, Dirkje S Postma, H Marike Boezen, Pim A De Jong, Marc Decramer, Jan-Willem J Lammers, Diether Lambrechts, Pieter Zanen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23349703/pdf/?tool=EBI
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author Firdaus A A Mohamed Hoesein
Els Wauters
Wim Janssens
Harry J M Groen
Joanna Smolonska
Cisca Wijmenga
Dirkje S Postma
H Marike Boezen
Pim A De Jong
Marc Decramer
Jan-Willem J Lammers
Diether Lambrechts
Pieter Zanen
author_facet Firdaus A A Mohamed Hoesein
Els Wauters
Wim Janssens
Harry J M Groen
Joanna Smolonska
Cisca Wijmenga
Dirkje S Postma
H Marike Boezen
Pim A De Jong
Marc Decramer
Jan-Willem J Lammers
Diether Lambrechts
Pieter Zanen
author_sort Firdaus A A Mohamed Hoesein
collection DOAJ
description Genetic variation in nicotinic acetylcholine receptor subunit genes (nAChRs) is associated with lung function level and chronic obstructive pulmonary disease (COPD). It is unknown whether these variants also predispose to an accelerated lung function decline. We investigated the association of nAChR susceptibility variants with lung function decline and COPD severity. The rs1051730 and rs8034191 variants were genotyped in a population-based cohort of 1,226 heavy smokers (COPACETIC) and in an independent cohort of 883 heavy smokers, of which 653 with COPD of varying severity (LEUVEN). Participants underwent pulmonary function tests at baseline. Lung function decline was assessed over a median follow-up of 3 years in COPACETIC. Current smokers homozygous for the rs1051730 A-allele or rs8034191 G-allele had significantly greater FEV(1)/FVC decline than homozygous carriers of wild-type alleles (3.3% and 4.3%, p = 0.026 and p = 0.009, respectively). In the LEUVEN cohort, rs1051730 AA-carriers and rs8034191 GG-carriers had a two-fold increased risk to suffer from COPD GOLD IV (OR 2.29, 95% confidence interval [CI] = 1.11-4.75; p = 0.025 and OR = 2.42, 95% [CI] = 1.18-4.95; p = 0.016, respectively). The same risk alleles conferred, respectively, a five- and four-fold increased risk to be referred for lung transplantation because of end-stage COPD (OR = 5.0, 95% [CI] = 1.68-14.89; p = 0.004 and OR = 4.06, 95% [CI] = 1.39-11.88; p = 0.010). In Europeans, variants in nAChRs associate with an accelerated lung function decline in current smokers and with clinically relevant COPD.
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spelling doaj.art-a9e120c027844384973e9562aa39e0622022-12-21T22:42:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5321910.1371/journal.pone.0053219Variants in the 15q24/25 locus associate with lung function decline in active smokers.Firdaus A A Mohamed HoeseinEls WautersWim JanssensHarry J M GroenJoanna SmolonskaCisca WijmengaDirkje S PostmaH Marike BoezenPim A De JongMarc DecramerJan-Willem J LammersDiether LambrechtsPieter ZanenGenetic variation in nicotinic acetylcholine receptor subunit genes (nAChRs) is associated with lung function level and chronic obstructive pulmonary disease (COPD). It is unknown whether these variants also predispose to an accelerated lung function decline. We investigated the association of nAChR susceptibility variants with lung function decline and COPD severity. The rs1051730 and rs8034191 variants were genotyped in a population-based cohort of 1,226 heavy smokers (COPACETIC) and in an independent cohort of 883 heavy smokers, of which 653 with COPD of varying severity (LEUVEN). Participants underwent pulmonary function tests at baseline. Lung function decline was assessed over a median follow-up of 3 years in COPACETIC. Current smokers homozygous for the rs1051730 A-allele or rs8034191 G-allele had significantly greater FEV(1)/FVC decline than homozygous carriers of wild-type alleles (3.3% and 4.3%, p = 0.026 and p = 0.009, respectively). In the LEUVEN cohort, rs1051730 AA-carriers and rs8034191 GG-carriers had a two-fold increased risk to suffer from COPD GOLD IV (OR 2.29, 95% confidence interval [CI] = 1.11-4.75; p = 0.025 and OR = 2.42, 95% [CI] = 1.18-4.95; p = 0.016, respectively). The same risk alleles conferred, respectively, a five- and four-fold increased risk to be referred for lung transplantation because of end-stage COPD (OR = 5.0, 95% [CI] = 1.68-14.89; p = 0.004 and OR = 4.06, 95% [CI] = 1.39-11.88; p = 0.010). In Europeans, variants in nAChRs associate with an accelerated lung function decline in current smokers and with clinically relevant COPD.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23349703/pdf/?tool=EBI
spellingShingle Firdaus A A Mohamed Hoesein
Els Wauters
Wim Janssens
Harry J M Groen
Joanna Smolonska
Cisca Wijmenga
Dirkje S Postma
H Marike Boezen
Pim A De Jong
Marc Decramer
Jan-Willem J Lammers
Diether Lambrechts
Pieter Zanen
Variants in the 15q24/25 locus associate with lung function decline in active smokers.
PLoS ONE
title Variants in the 15q24/25 locus associate with lung function decline in active smokers.
title_full Variants in the 15q24/25 locus associate with lung function decline in active smokers.
title_fullStr Variants in the 15q24/25 locus associate with lung function decline in active smokers.
title_full_unstemmed Variants in the 15q24/25 locus associate with lung function decline in active smokers.
title_short Variants in the 15q24/25 locus associate with lung function decline in active smokers.
title_sort variants in the 15q24 25 locus associate with lung function decline in active smokers
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23349703/pdf/?tool=EBI
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