Literature DB >> 27612410

Genome-wide association study on the FEV1/FVC ratio in never-smokers identifies HHIP and FAM13A.

Diana A van der Plaat1, Kim de Jong1, Lies Lahousse2, Alen Faiz3, Judith M Vonk1, Cleo C van Diemen4, Ivana Nedeljkovic5, Najaf Amin5, Guy G Brusselle6, Albert Hofman5, Corry-Anke Brandsma3, Yohan Bossé7, Don D Sin8, David C Nickle9, Cornelia M van Duijn5, Dirkje S Postma10, H Marike Boezen11.   

Abstract

BACKGROUND: Although a striking proportion (25% to 45%) of patients with chronic obstructive pulmonary disease are never-smokers, most genetic susceptibility studies have not focused on this group exclusively.
OBJECTIVE: The aim of this study was to identify common genetic variants associated with FEV1 and its ratio to forced vital capacity (FVC) in never-smokers.
METHODS: Genome-wide association studies were performed in 5070 never-smokers of the identification cohort LifeLines, and results (P < 10-5) were verified by using a meta-analysis of the Vlagtwedde-Vlaardingen study and the Rotterdam Study I-III (total n = 1966). Furthermore, we aimed to assess the effects of the replicated variants in more detail by performing genetic risk score, expression quantitative trait loci, and variant*ever-smoking interaction analyses.
RESULTS: We identified associations between the FEV1/FVC ratio and 5 common genetic variants in the identification cohort, and 2 of these associations were replicated. The 2 variants annotated to the genes hedgehog interacting protein (HHIP) and family with sequence similarity 13 member A (FAM13A) were shown to have an additive effect on FEV1/FVC levels in the genetic risk score analysis; were associated with gene expression of HHIP and FAM13A in lung tissue, respectively; and were genome-wide significant in a meta-analysis including both identification and 4 verification cohorts (P < 2.19 × 10-7). Finally, we did not identify significant interactions between the variants and ever smoking. Results of the FEV1 identification analysis were not replicated.
CONCLUSION: The genes HHIP and FAM13A confer a risk for airway obstruction in general that is not driven exclusively by cigarette smoking, which is the main risk factor for chronic obstructive pulmonary disease.
Copyright © 2016 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Genome-wide association study; chronic obstructive pulmonary disease; genetics; never-smokers; pulmonary function

Mesh:

Substances:

Year:  2016        PMID: 27612410     DOI: 10.1016/j.jaci.2016.06.062

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  20 in total

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9.  A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants.

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10.  No association between DNA methylation and COPD in never and current smokers.

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