Are myocardial infarction-associated single nucleotide polymorphisms associated with ischemic stroke?
Cheng, Yu-Ching, Anderson, Christopher D., Bione, Silvia, Keene, Keith, Maguire, Jane M., Nalls, Michael, Rasheed, Asif, Zeginigg, Marion, Attia, John, Baker, Ross, Barlera, Simona, Biffi, Alessandro, Bookman, Ebony, Brott, Thomas G., Brown, Robert D., Chen , Fang, Chen, Wei-Min, Ciusani, Emilio, Cole, John W., Cortellini, Lynelle, Danesh, John, Doheny, Kimberly, Ferrucci, Luigi, Franzosi, Maria Grazia, Frosshard, Philippe, Furie, Karen L., Golledge, Jonathan, Hankey, Graeme J., Hernandez, Dena, Holliday, Elizabeth G., Hsu , Fang-Chi, Jannes, Jim, Kamal, Ayeesha, Khan, Muhammad Saleem, Kittner, Steven J., Koblar, Simon A., Lewis, Martin, Lincz, Lisa, Lisa, Antonella, Matarin, Mar, Moscato, Pablo, Mychaleckyj, Josyf C., Parati, Eugenio A., Parolo, Silvia, Pugh, Elizabeth, Rost, Natalia S., Schallert, Michael, Schmidt, Helena, Scott, Rodney J., Sturm, Jonathan W., Yadav, Sunaina, Zaidi, Moazzam, Boncoraglio, Giorgio B., Levi, Christopher Royce, Meschia, James F., Rosand, Jonathan, Sale, Michele, Saleheen, Danish, Schmidt, Reinhold, Sharma, Pankaj, Worrall, Bradford, Mitchell, Braxton D., GARNET Collaborative Research Group, , and GENEVA Consortium, (2012) Are myocardial infarction-associated single nucleotide polymorphisms associated with ischemic stroke? Stroke, 43 (4). pp. 980-986.
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Background and Purpose: Ischemic stroke (IS) shares many common risk factors with coronary artery disease (CAD). We hypothesized that genetic variants associated with myocardial infarction (MI) or CAD may be similarly involved in the etiology of IS. To test this hypothesis, we evaluated whether single-nucleotide polymorphisms (SNPs) at 11 different loci recently associated with MI or CAD through genome-wide association studies were associated with IS.
Methods: Meta-analyses of the associations between the 11 MI-associated SNPs and IS were performed using 6865 cases and 11 395 control subjects recruited from 9 studies. SNPs were either genotyped directly or imputed; in a few cases a surrogate SNP in high linkage disequilibrium was chosen. Logistic regression was performed within each study to obtain study-specific βs and standard errors. Meta-analysis was conducted using an inverse variance weighted approach assuming a random effect model.
Results: Despite having power to detect odds ratio of 1.09–1.14 for overall IS and 1.20–1.32 for major stroke subtypes, none of the SNPs were significantly associated with overall IS and/or stroke subtypes after adjusting for multiple comparisons.
Conclusions: Our results suggest that the major common loci associated with MI risk do not have effects of similar magnitude on overall IS but do not preclude moderate associations restricted to specific IS subtypes. Disparate mechanisms may be critical in the development of acute ischemic coronary and cerebrovascular events.
|Item Type:||Article (Refereed Research - C1)|
"on behalf of the International Stroke Genetics Consortium"
|Date Deposited:||04 Jun 2012 05:37|
|FoR Codes:||11 MEDICAL AND HEALTH SCIENCES > 1102 Cardiovascular Medicine and Haematology > 110201 Cardiology (incl Cardiovascular Diseases) @ 100%|
|SEO Codes:||92 HEALTH > 9201 Clinical Health (Organs, Diseases and Abnormal Conditions) > 920103 Cardiovascular System and Diseases @ 100%|
|Citation Count from Web of Science||
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