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Genome-wide study of percent emphysema on computed tomography in the general population

Authors :
James D. Crapo
Adam Wanner
Matthew J. Budoff
Mark L. Brantly
Rhea E. Powell
Eric A. Hoffman
J. Jeffrey Carr
Harry J.M. Groen
Michael H. Cho
Heather Baumhauer
Dirkje S. Postma
Pieter Zanen
Wei Gao
John E. Hokanson
H. Marike Boezen
Leslie J. Raffel
Terri H. Beaty
Edwin K. Silverman
George R. Washko
George T. O'Connor
Joel D. Kaufman
Tess D. Pottinger
Joanna Smolonska
Cisca Wijmenga
Charles A. Powell
John H. M. Austin
Josée Dupuis
Daniel Rabinowitz
Ani Manichaikul
R. Graham Barr
Karen Hinckley Stukovsky
Benjamin M. Smith
Stephen S. Rich
Farshid N. Rouhani
Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI)
Damage and Repair in Cancer Development and Cancer Treatment (DARE)
Guided Treatment in Optimal Selected Cancer Patients (GUTS)
Groningen Research Institute for Asthma and COPD (GRIAC)
Life Course Epidemiology (LCE)
Source :
American Journal of Respiratory and Critical Care Medicine, 189(4), 408-418. AMER THORACIC SOC, American journal of respiratory and critical care medicine, vol 189, iss 4
Publication Year :
2014

Abstract

RationalePulmonary emphysema overlaps partially with spirometrically defined chronic obstructive pulmonary disease and is heritable, with moderately high familial clustering.ObjectivesTo complete a genome-wide association study (GWAS) for the percentage of emphysema-like lung on computed tomography in the Multi-Ethnic Study of Atherosclerosis (MESA) Lung/SNP Health Association Resource (SHARe) Study, a large, population-based cohort in the United States.MethodsWe determined percent emphysema and upper-lower lobe ratio in emphysema defined by lung regions less than -950 HU on cardiac scans. Genetic analyses were reported combined across four race/ethnic groups: non-Hispanic white (n = 2,587), African American (n = 2,510), Hispanic (n = 2,113), and Chinese (n = 704) and stratified by race and ethnicity.Measurements and main resultsAmong 7,914 participants, we identified regions at genome-wide significance for percent emphysema in or near SNRPF (rs7957346; P = 2.2 × 10(-8)) and PPT2 (rs10947233; P = 3.2 × 10(-8)), both of which replicated in an additional 6,023 individuals of European ancestry. Both single-nucleotide polymorphisms were previously implicated as genes influencing lung function, and analyses including lung function revealed independent associations for percent emphysema. Among Hispanics, we identified a genetic locus for upper-lower lobe ratio near the α-mannosidase-related gene MAN2B1 (rs10411619; P = 1.1 × 10(-9); minor allele frequency [MAF], 4.4%). Among Chinese, we identified single-nucleotide polymorphisms associated with upper-lower lobe ratio near DHX15 (rs7698250; P = 1.8 × 10(-10); MAF, 2.7%) and MGAT5B (rs7221059; P = 2.7 × 10(-8); MAF, 2.6%), which acts on α-linked mannose. Among African Americans, a locus near a third α-mannosidase-related gene, MAN1C1 (rs12130495; P = 9.9 × 10(-6); MAF, 13.3%) was associated with percent emphysema.ConclusionsOur results suggest that some genes previously identified as influencing lung function are independently associated with emphysema rather than lung function, and that genes related to α-mannosidase may influence risk of emphysema.

Details

Language :
English
ISSN :
1073449X
Volume :
189
Issue :
4
Database :
OpenAIRE
Journal :
American Journal of Respiratory and Critical Care Medicine
Accession number :
edsair.doi.dedup.....a824bda61529f6275b65870bb7d11066