Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/16805
Title: Genome-wide association study identifies five loci associated with lung function.
Authors: Repapi, E
Sayers, I
Wain, LV
Burton, PR
Johnson, T
Obeidat, M
Zhao, JH
Ramasamy, A
Zhai, G
Vitart, V
Huffman, JE
Igl, W
Albrecht, E
Deloukas, P
Henderson, J
Granell, R
McArdle, WL
Rudnicka, AR
Wellcome Trust Case Control Consortium
Barroso, I
Loos, RJ
Wareham, NJ
Mustelin, L
Rantanen, T
Surakka, I
Imboden, M
Wichmann, HE
Grkovic, I
Jankovic, S
Zgaga, L
Hartikainen, AL
Peltonen, L
Gyllensten, U
Johansson, A
Zaboli, G
Campbell, H
Wild, SH
Wilson, JF
Gläser, S
Homuth, G
Völzke, H
Mangino, M
Soranzo, N
Spector, TD
Polasek, O
Rudan, I
Wright, AF
Heliövaara, M
Ripatti, S
Pouta, A
Naluai, AT
Olin, AC
Torén, K
Cooper, MN
James, AL
Palmer, LJ
Hingorani, AD
Wannamethee, SG
Whincup, PH
Smith, GD
Ebrahim, S
McKeever, TM
Pavord, ID
MacLeod, AK
Morris, AD
Porteous, DJ
Cooper, C
Dennison, E
Shaheen, S
Karrasch, S
Schnabel, E
Schulz, H
Grallert, H
Bouatia-Naji, N
Delplanque, J
Froguel, P
Blakey, JD
NSHD Respiratory Study Team
Britton, JR
Morris, RW
Holloway, JW
Lawlor, DA
Hui, J
Nyberg, F
Jarvelin, MR
Jackson, C
Kähönen, M
Kaprio, J
Probst-Hensch, NM
Koch, B
Hayward, C
Evans, DM
Elliott, P
Strachan, DP
Hall, IP
Tobin, MD
First Published: Jan-2010
Citation: NAT GENET, 2010, 42 (1), pp. 36-44
Abstract: Pulmonary function measures are heritable traits that predict morbidity and mortality and define chronic obstructive pulmonary disease (COPD). We tested genome-wide association with forced expiratory volume in 1 s (FEV(1)) and the ratio of FEV(1) to forced vital capacity (FVC) in the SpiroMeta consortium (n = 20,288 individuals of European ancestry). We conducted a meta-analysis of top signals with data from direct genotyping (n < or = 32,184 additional individuals) and in silico summary association data from the CHARGE Consortium (n = 21,209) and the Health 2000 survey (n < or = 883). We confirmed the reported locus at 4q31 and identified associations with FEV(1) or FEV(1)/FVC and common variants at five additional loci: 2q35 in TNS1 (P = 1.11 x 10(-12)), 4q24 in GSTCD (2.18 x 10(-23)), 5q33 in HTR4 (P = 4.29 x 10(-9)), 6p21 in AGER (P = 3.07 x 10(-15)) and 15q23 in THSD4 (P = 7.24 x 10(-15)). mRNA analyses showed expression of TNS1, GSTCD, AGER, HTR4 and THSD4 in human lung tissue. These associations offer mechanistic insight into pulmonary function regulation and indicate potential targets for interventions to alleviate respiratory disease.
DOI Link: 10.1038/ng.501
eISSN: 1546-1718
Links: http://hdl.handle.net/2381/16805
Type: Journal Article
Appears in Collections:Published Articles, Dept. of Health Sciences

Files in This Item:
There are no files associated with this item.


Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.