Exploring the interaction among EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han population

被引:8
作者
An, Li [1 ]
Lin, Yingxiang [1 ]
Yang, Ting [2 ]
Hua, Lin [3 ,4 ]
机构
[1] Capital Med Univ, Beijing Key Lab Resp & Pulm Circulat Disorders, Beijing Inst Resp Med, Dept Resp & Crit Care Med,Beijing Chao Yang Hosp, Beijing 100020, Peoples R China
[2] China Japan Friendship Hosp, Dept Resp & Crit Care Med, Beijing 100029, Peoples R China
[3] Capital Med Univ, Sch Biomed Engn, Beijing 100069, Peoples R China
[4] Capital Med Univ, Beijing Key Lab Fundamental Res Biomech Clin Appl, Sch Biomed Engn, Beijing 100069, Peoples R China
基金
北京市自然科学基金; 美国国家科学基金会;
关键词
COPD; SNP; Interaction; Quantitative traits; MDR; MULTIFACTOR DIMENSIONALITY REDUCTION; MICROSOMAL EPOXIDE HYDROLASE; LUNG-FUNCTION; GENETIC-VARIANTS; POLYMORPHISMS; ASSOCIATION; EMPHYSEMA; PATHWAYS; CAPACITY; DYSPNEA;
D O I
10.1186/s40246-016-0076-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Currently, the majority of genetic association studies on chronic obstructive pulmonary disease (COPD) risk focused on identifying the individual effects of single nucleotide polymorphisms (SNPs) as well as their interaction effects on the disease. However, conventional genetic studies often use binary disease status as the primary phenotype, but for COPD, many quantitative traits have the potential correlation with the disease status and closely reflect pathological changes. Method: Here, we genotyped 44 SNPs from four genes (EPHX1, GSTP1, SERPINE2, and TGFB1) in 310 patients and 203 controls which belonged to the Chinese Han population to test the two-way and three-way genetic interactions with COPD-related quantitative traits using recently developed generalized multifactor dimensionality reduction (GMDR) and quantitative multifactor dimensionality reduction (QMDR) algorithms. Results: Based on the 310 patients and the whole samples of 513 subjects, the best gene-gene interactions models were detected for four lung-function-related quantitative traits. For the forced expiratory volume in 1 s (FEV1), the best interaction was seen from EPHX1, SERPINE2, and GSTP1. For FEV1% pre, the forced vital capacity (FVC), and FEV1/FVC, the best interactions were seen from SERPINE2 and TGFB1. Conclusion: The results of this study provide further evidence for the genotype combinations at risk of developing COPD in Chinese Han population and improve the understanding on the genetic etiology of COPD and COPD-related quantitative traits.
引用
收藏
页数:12
相关论文
共 35 条
[1]   Association of SERPINE2 gene with the risk of chronic obstructive pulmonary disease and spirometric phenotypes in northern Han Chinese population [J].
An, Li ;
Yang, Ting ;
Zhang, Yongbiao ;
Lin, Yingxiang ;
Zhang, Hong ;
Jiao, Xia ;
Hua, Lin ;
Dai, Huaping ;
Wang, Chen .
MOLECULAR BIOLOGY REPORTS, 2012, 39 (02) :1427-1433
[2]   Effect of Five Genetic Variants Associated with Lung Function on the Risk of Chronic Obstructive Lung Disease, and Their Joint Effects on Lung Function [J].
Artigas, Maria Soler ;
Wain, Louise V. ;
Repapi, Emmanouela ;
Obeidat, Ma'en ;
Sayers, Ian ;
Burton, Paul R. ;
Johnson, Toby ;
Zhao, Jing Hua ;
Albrecht, Eva ;
Dominiczak, Anna F. ;
Kerr, Shona M. ;
Smith, Blair H. ;
Cadby, Gemma ;
Hui, Jennie ;
Palmer, Lyle J. ;
Hingorani, Aroon D. ;
Wannamethee, S. Goya ;
Whincup, Peter H. ;
Ebrahim, Shah ;
Smith, George Davey ;
Barroso, Ines ;
Loos, Ruth J. F. ;
Wareham, Nicholas J. ;
Cooper, Cyrus ;
Dennison, Elaine ;
Shaheen, Seif O. ;
Liu, Jason Z. ;
Marchini, Jonathan ;
Dahgam, Santosh ;
Naluai, Asa Torinsson ;
Olin, Anna-Carin ;
Karrasch, Stefan ;
Heinrich, Joachim ;
Schulz, Holger ;
McKeever, Tricia M. ;
Pavord, Ian D. ;
Heliovaara, Markku ;
Ripatti, Samuli ;
Surakka, Ida ;
Blakey, John D. ;
Kahonen, Mika ;
Britton, John R. ;
Nyberg, Fredrik ;
Holloway, John W. ;
Lawlor, Debbie A. ;
Morris, Richard W. ;
James, Alan L. ;
Jackson, Cathy M. ;
Hall, Ian P. ;
Tobin, Martin D. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2011, 184 (07) :786-795
[3]   Usefulness of the Medical Research Council (MRC) dyspnoea scale as a measure of disability in patients with chronic obstructive pulmonary disease [J].
Bestall, JC ;
Paul, EA ;
Garrod, R ;
Garnham, R ;
Jones, PW ;
Wedzicha, JA .
THORAX, 1999, 54 (07) :581-586
[4]   Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario [J].
Briollais, Laurent ;
Wang, Yuanyuan ;
Rajendram, Isaac ;
Onay, Venus ;
Shi, Ellen ;
Knight, Julia ;
Ozcelik, Hilmi .
BMC MEDICINE, 2007, 5 (1)
[5]   The body-mass index, airflow obstruction, dyspnea, and exercise capacity index in chronic obstructive pulmonary disease [J].
Celli, BR ;
Cote, CG ;
Marin, JM ;
Casanova, C ;
de Oca, MM ;
Mendez, RA ;
Pinto Plata, V ;
Cabral, HJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (10) :1005-1012
[6]   Genetic variants of microsomal epoxide hydrolase and glutamate-cysteine ligase in COPD [J].
Chappell, S. ;
Daly, L. ;
Morgan, K. ;
Guetta-Baranes, T. ;
Roca, J. ;
Rabinovich, R. ;
Lotya, J. ;
Millar, A. B. ;
Donnelly, S. C. ;
Keatings, V. ;
MacNee, W. ;
Stolk, J. ;
Hiemstra, P. S. ;
Miniati, M. ;
Monti, S. ;
O'Connor, C. M. ;
Kalshelker, N. .
EUROPEAN RESPIRATORY JOURNAL, 2008, 32 (04) :931-937
[7]   ATS statement: Guidelines for the six-minute walk test [J].
Crapo, RO ;
Casaburi, R ;
Coates, AL ;
Enright, PL ;
MacIntyre, NR ;
McKay, RT ;
Johnson, D ;
Wanger, JS ;
Zeballos, RJ ;
Bittner, V ;
Mottram, C .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (01) :111-117
[8]   FOS IMMUNOREACTIVITY ASSESSMENT ON HUMAN NORMAL AND PATHOLOGICAL BRONCHIAL BIOPSIES [J].
DEMOLY, P ;
CHANEZ, P ;
PUJOL, JL ;
GAUTHIERROUVIERE, C ;
MICHEL, FB ;
GODARD, P ;
BOUSQUET, J .
RESPIRATORY MEDICINE, 1995, 89 (05) :329-335
[9]   Polymorphism of SERPINE2 gene is associated with pulmonary emphysema in consecutive autopsy cases [J].
Fujimoto, Koichi ;
Ikeda, Shinobu ;
Arai, Tomio ;
Tanaka, Noriko ;
Kumasaka, Toshio ;
Ishii, Takeo ;
Kida, Kozui ;
Muramatsu, Masaaki ;
Sawabe, Motoji .
BMC MEDICAL GENETICS, 2010, 11
[10]  
Regueiro EMG, 2009, CLINICS, V64, P983