Impact of a Genetic Risk Score on Myocardial Infarction Risk Across Different Ethnic Populations

被引:16
作者
Joseph, Philip G. [1 ]
Pare, Guillaume [1 ]
Asma, Senay [1 ]
Engert, James C. [2 ]
Yusuf, Salim [1 ]
Anand, Sonia S. [1 ]
机构
[1] McMaster Univ, Populat Hlth Res Inst, Hamilton, ON, Canada
[2] McGill Univ, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
CORONARY-HEART-DISEASE; GENOME-WIDE ASSOCIATION; CARDIOVASCULAR-DISEASE; 52; COUNTRIES; ATHEROSCLEROSIS; PREDICTION; INTERHEART; MUTATIONS;
D O I
10.1016/j.cjca.2016.05.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Myocardial infarction (MI) risk varies by ethnicity, although the influence of genetic factors remains unclear. Using a genetic risk score (GRS), we examined the association between 25 coronary artery disease (CAD)-related single nucleotide polymorphisms and MI across 6 ethnic groups. Methods: We studied 8556 participants in the INTERHEART case-control study from 6 ethnic groups: Europeans, South Asians, Southeast Asians, Arabs, Latin Americans, and Africans. Associations between the GRS and MI were tested in each group by logistic regression and overall by meta-analysis. Results: Overall, the GRS increased the odds of MI by 1.07 (95% confidence interval [CI], 1.04-1.09) per risk allele in the unadjusted model, with little change (odds ratio, 1.06; 95% CI, 1.04-1.09) after adjusting for demographic and modifiable factors. In Europeans, South Asians, Southeast Asians, and Arabs, the GRS was significantly associated with MI, with minimal heterogeneity observed. In these groups, a score > 23 risk alleles (highest 4 quintiles) was associated with only a 5% difference in population attributable risk (PAR) (36% to 41%) for MI. The GRS was not significant in Latin Americans or Africans. In the overall cohort, modest changes, beyond clinical factors, in PAR (88% to 91%), concordance statistic (0.73 to 0.74), and continuous net reclassification improvement (12%) were observed with the GRS. Conclusions: A CAD GRS is associated with MI across a multiethnic cohort, with significant and consistent effects across 4 distinct ethnicities. However, it only modestly improves MI risk prediction beyond clinical factors.
引用
收藏
页码:1440 / 1446
页数:7
相关论文
共 27 条
[21]   Genomewide association analysis of coronary artery disease [J].
Samani, Nilesh J. ;
Erdmann, Jeanette ;
Hall, Alistair S. ;
Hengstenberg, Christian ;
Mangino, Massimo ;
Mayer, Bjoern ;
Dixon, Richard J. ;
Meitinger, Thomas ;
Braund, Peter ;
Wichmann, H.-Erich ;
Barrett, Jennifer H. ;
Koenig, Inke R. ;
Stevens, Suzanne E. ;
Szymczak, Silke ;
Tregouet, David-Alexandre ;
Iles, Mark M. ;
Pahlke, Friedrich ;
Pollard, Helen ;
Lieb, Wolfgang ;
Cambien, Francois ;
Fischer, Marcus ;
Ouwehand, Willem ;
Blankenberg, Stefan ;
Balmforth, Anthony J. ;
Baessler, Andrea ;
Ball, Stephen G. ;
Strom, Tim M. ;
Braenne, Ingrid ;
Gieger, Christian ;
Deloukas, Panos ;
Tobin, Martin D. ;
Ziegler, Andreas ;
Thompson, John R. ;
Schunkert, Heribert .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (05) :443-453
[22]  
Schunkert H, 2011, NAT GENET, V43, P333, DOI 10.1161/CIRCGENETICS.111.960443
[23]   Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease [J].
Stitziel, Nathan O. ;
Won, Hong-Hee ;
Morrison, Alanna C. ;
Peloso, Gina M. ;
Do, Ron ;
Lange, Leslie A. ;
Fontanillas, Pierre ;
Gupta, Namrata ;
Duga, Stefano ;
Goel, Anuj ;
Farrall, Martin ;
Saleheen, Danish ;
Ferrario, Paola ;
Koenig, Inke ;
Asselta, Rosanna ;
Merlini, Piera A. ;
Marziliano, Nicola ;
Notarangelo, Maria Francesca ;
Schick, Ursula ;
Auer, Paul ;
Assimes, Themistocles L. ;
Reilly, Muredach ;
Wilensky, Robert ;
Rader, Daniel J. ;
Hovingh, G. Kees ;
Meitinger, Thomas ;
Kessler, Thorsten ;
Kastrati, Adnan ;
Laugwitz, Karl-Ludwig ;
Siscovick, David ;
Rotter, Jerome I. ;
Hazen, Stanley L. ;
Tracy, Russell ;
Cresci, Sharon ;
Spertus, John ;
Jackson, Rebecca ;
Schwartz, Stephen M. ;
Natarajan, Pradeep ;
Crosby, Jacy ;
Muzny, Donna ;
Ballantyne, Christie ;
Rich, Stephen S. ;
O'Donnell, Christopher J. ;
Abecasis, Goncalo ;
Sunyaev, Shamil ;
Nickerson, Deborah A. ;
Buring, Julie E. ;
Ridker, Paul M. ;
Chasman, Daniel I. ;
Austin, Erin .
NEW ENGLAND JOURNAL OF MEDICINE, 2014, 371 (22) :2072-2082
[24]   A Genetic Risk Score Is Associated With Incident Cardiovascular Disease and Coronary Artery Calcium The Framingham Heart Study [J].
Thanassoulis, George ;
Peloso, Gina M. ;
Pencina, Michael J. ;
Hoffmann, Udo ;
Fox, Caroline S. ;
Cupples, L. Adrienne ;
Levy, Daniel ;
D'Agostino, Ralph B., Sr. ;
Hwang, Shih-Jen ;
O'Donnell, Christopher J. .
CIRCULATION-CARDIOVASCULAR GENETICS, 2012, 5 (01) :113-121
[25]   Accounting for ancestry: population substructure and genome-wide association studies [J].
Tian, Chao ;
Gregersen, Peter K. ;
Seldin, Michael F. .
HUMAN MOLECULAR GENETICS, 2008, 17 :R143-R150
[26]   Literature-Based Genetic Risk Scores for Coronary Heart Disease The Cardiovascular Registry Maastricht (CAREMA) Prospective Cohort Study [J].
Vaarhorst, Anika A. M. ;
Lu, Yingchang ;
Heijmans, Bastiaan T. ;
Dolle, Martijn E. T. ;
Boehringer, Stefan ;
Putter, Hein ;
Imholz, Sandra ;
Merry, Audrey H. H. ;
van Greevenbroek, Marleen M. ;
Jukema, J. Wouter ;
Gorgels, Anton P. M. ;
van den Brandt, Piet A. ;
Mueller, Michael ;
Schouten, Leo J. ;
Feskens, Edith J. M. ;
Boer, Jolanda M. A. ;
Slagboom, P. Eline .
CIRCULATION-CARDIOVASCULAR GENETICS, 2012, 5 (02) :202-209
[27]   Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study [J].
Yusuf, S ;
Hawken, S ;
Ounpuu, S ;
Dans, T ;
Avezum, A ;
Lanas, F ;
McQueen, M ;
Budaj, A ;
Pais, P ;
Varigos, J ;
Liu, LS .
LANCET, 2004, 364 (9438) :937-952