Conditional Inference Tree for Multiple Gene-Environment Interactions on Myocardial Infarction

被引:8
作者
Wu, Zhijun [1 ]
Su, Xiuxiu [1 ]
Sheng, Haihui [2 ]
Chen, Yanjia [1 ]
Gao, Xiang [3 ]
Bao, Le [4 ]
Jin, Wei [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Cardiol, 197 Ruijin Er Rd, Shanghai 200025, Peoples R China
[2] Natl Engn Ctr Biochip Shanghai, Shanghai, Peoples R China
[3] Penn State Univ, Dept Nutr Sci, State Coll, PA USA
[4] Penn State Univ, Dept Stat, State Coll, PA USA
基金
中国国家自然科学基金;
关键词
Data mining; Conditional inference tree; Myocardial infarction; Genome wide association study; GENOME-WIDE ASSOCIATION; CORONARY-ARTERY-DISEASE; TASK-FORCE; RISK; CLASSIFICATION; LOCI; SUSCEPTIBILITY; ATHEROSCLEROSIS; POLYMORPHISMS; STRATEGIES;
D O I
10.1016/j.arcmed.2017.12.001
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background and Aims. Identifying gene-environment interaction in the context of multiple environmental factors has been a challenging task. We aimed to use conditional inference tree (CTREE) to strata myocardial infarction (MI) risk synthesizing information from both genetic and environmental factors. Methods. We conducted a case-control study including 1440 Chinese men (730 MI patients and 710 controls). We first calculated a weighted genetic risk score (GRS) by combining 25 single nucleotide polymorphisms (SNPs) that had been identified to be associated with coronary artery diseases in previous genome wide association studies. We then developed a CTREE model to interpret the gene-environment interaction network in predicting MI. Results. We detected high-order interactions between dyslipidemia, GRS, smoking status, age and diabetes. Of all the variables examined, high density lipoprotein cholesterol (HDL-C) of <= 1.25 mmlo/L was identified as the key discriminator. The subsequent splits of MI were low density lipoprotein cholesterol (LDL-C) of 4.01 mmol/L and GRS of 20.9. We found that individuals with HDL-C <= 1.25 mmol/L, GRS >20.9 and lipoprotein (a) > 0.09 g/L had a higher risk of MI than those who at the lowest risk group (OR: 5.89, 95% CI: 3.99-8.69). This magnitude of MI risk was similar to the combination of HDL-C 51.25 mmol/L, GRS <= 20.9, smoking and lipoprotein (a) > 0.15 g/L (OR: 5.49, 95% CI: 3.51-8.58). Conclusions. The multiple interactions between genetic and environmental factors can be visually present via the CTREE approach. The tree diagram also simplifies the decision making procedure by answering a sequence of questions along the branches. (C) 2017 IMSS. Published by Elsevier Inc.
引用
收藏
页码:546 / 552
页数:7
相关论文
共 43 条
  • [1] Large Scale Association Analysis of Novel Genetic Loci for Coronary Artery Disease
    Amouyel, Philippe
    Arveiler, Dominique
    Boekholdt, S. Matthijs
    Braund, Peter
    Bruse, Petra
    Bumpstead, Suzannah J.
    Bugert, Peter
    Cambien, Francois
    Danesh, John
    Deloukas, Panos
    Doering, Angela
    Ducimetiere, Pierre
    Dunn, Ruth M.
    El Mokhtari, Nour-Eddine
    Erdmann, Jeanette
    Evans, Alun
    Ewels, Phil
    Ferrieres, Jean
    Fischer, Marcus
    Frossard, Philippe
    Garner, Stephen
    Gieger, Christian
    Gohri, Mohammed J. R.
    Goodall, Alison H.
    Grosshennig, Anika
    Hall, Alistair
    Hardwick, Rob
    Haukijarvi, Ari
    Hengstenberg, Christian
    Illig, Thomas
    Karvanen, Juha
    Kastelein, John
    Kee, Frank
    Khaw, Kay-Tee
    Klueter, Harald
    Koenig, Inke R.
    Kuulasmaa, Kari
    Laiho, Paivi
    Luc, Gerald
    Maerz, Winfried
    McGinnis, Ralph
    McLaren, William
    Meisinger, Christa
    Morrison, Caroline
    Ou, Xiodan
    Ouwehand, Willem H.
    Preuss, Michael
    Proust, Carole
    Ravindrarajah, Radhi
    Renner, Wilfried
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2009, 29 (05) : 774 - U356
  • [2] 2011 ACCF/AHA Focused Update Incorporated Into the ACC/AHA 2007 Guidelines for the Management of Patients With Unstable Angina/Non-ST-Elevation Myocardial Infarction: A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines
    Anderson, Jeffrey L.
    Adams, Cynthia D.
    Antman, Elliott M.
    Bridges, Charles R.
    Califf, Robert M.
    Casey, Donald E., Jr.
    Chavey, William E., II
    Fesmire, Francis M.
    Hochman, Judith S.
    Levin, Thomas N.
    Lincoff, A. Michael
    Peterson, Eric D.
    Theroux, Pierre
    Wenger, Nanette Kass
    Wright, R. Scott
    Ettinger, Steven M.
    Ganiats, Theodore G.
    Jneid, Hani
    Philippides, George J.
    Zidar, James Patrick
    Jacobs, Alice K.
    Albert, Nancy
    Hochman, Judith S.
    Creager, Mark A.
    Kushner, Frederick G.
    Ohman, Erik Magnus
    Guyton, Robert A.
    Stevenson, William G.
    Halperin, Jonathan L.
    Yancy, Clyde W.
    [J]. CIRCULATION, 2011, 123 (18) : E426 - E579
  • [3] [Anonymous], PARTY LAB RECURSIVE
  • [4] Decision Tree-Based Modeling of Androgen Pathway Genes and Prostate Cancer Risk
    Barnholtz-Sloan, Jill S.
    Guan, Xiaowei
    Zeigler-Johnson, Charnita
    Meropol, Neal J.
    Rebbeck, Timothy R.
    [J]. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2011, 20 (06) : 1146 - 1155
  • [5] Breiman F, 1984, OLSHEN STONE CLASSIF
  • [6] Genome-wide association study validation identifies novel loci for atherosclerotic cardiovascular disease
    Chen, X.
    Li, S.
    Yang, Y.
    Yang, X.
    Liu, Y.
    Liu, Y.
    Hu, W.
    Jin, L.
    Wang, X.
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2012, 10 (08) : 1508 - 1514
  • [7] Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease
    Clarke, Robert
    Peden, John F.
    Hopewell, Jemma C.
    Kyriakou, Theodosios
    Goel, Anuj
    Heath, Simon C.
    Parish, Sarah
    Barlera, Simona
    Franzosi, Maria Grazia
    Rust, Stephan
    Bennett, Derrick
    Silveira, Angela
    Malarstig, Anders
    Green, Fiona R.
    Lathrop, Mark
    Gigante, Bruna
    Leander, Karin
    de Faire, Ulf
    Seedorf, Udo
    Hamsten, Anders
    Collins, Rory
    Watkins, Hugh
    Farrall, Martin
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (26) : 2518 - 2528
  • [8] Crow JF, 1999, GENETICS, V152, P821
  • [9] The use of meta-analysis risk estimates for candidate genes in combination to predict coronary heart disease risk
    Drenos, F.
    Whittaker, J. C.
    Humphries, S. E.
    [J]. ANNALS OF HUMAN GENETICS, 2007, 71 : 611 - 619
  • [10] Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23
    Erdmann, Jeanette
    Willenborg, Christina
    Nahrstaedt, Janja
    Preuss, Michael
    Koenig, Inke R.
    Baumert, Jens
    Linsel-Nitschke, Patrick
    Gieger, Christian
    Tennstedt, Stephanie
    Belcredi, Petra
    Aherrahrou, Zouhair
    Klopp, Norman
    Loley, Christina
    Stark, Klaus
    Hengstenberg, Christian
    Bruse, Petra
    Freyer, Jennifer
    Wagner, Arnika K.
    Medack, Anja
    Lieb, Wolfgang
    Grosshennig, Anika
    Sager, Hendrik B.
    Reinhardt, Adrian
    Schaefer, Arne
    Schreiber, Stefan
    El Mokhtari, Nour Eddine
    Raaz-Schrauder, Dorette
    Illig, Thomas
    Garlichs, Christoph D.
    Ekici, Arif B.
    Reis, Andre
    Schrezenmeir, Juergen
    Rubin, Diana
    Ziegler, Andreas
    Wichmann, H. -E.
    Doering, Angela
    Meisinger, Christa
    Meitinger, Thomas
    Peters, Annette
    Schunkert, Heribert
    [J]. EUROPEAN HEART JOURNAL, 2011, 32 (02) : 158 - 168