Literature DB >> 22322877

Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease.

Salim S Virani1, Ariel Brautbar, Vei-Vei Lee, Elayda MacArthur, Alanna C Morrison, Megan L Grove, Vijay Nambi, Lorraine Frazier, James M Wilson, James T Willerson, Eric Boerwinkle, Christie M Ballantyne.   

Abstract

BACKGROUND: Chromosome 9p21 single nucleotide polymorphisms (SNPs) have been shown to be associated with coronary heart disease in multiple studies. The aim of the present study was to identify whether these SNPs are associated with recurrent myocardial infarction (MI), revascularization, or death in acute coronary syndrome (ACS) patients or in those undergoing coronary artery bypass grafting (CABG). METHODS AND
RESULTS: TexGen registry participants with ACS (n=2,067) or CABG (n=1,176) were evaluated, to assess whether 9p21 SNPs (rs1333049, rs2383206, rs10757278, rs10757274) were associated with recurrent MI (primary outcome), recurrent revascularization, or death (secondary outcomes) at approximately 3.2 years of follow-up. Carriers of risk allele (C) for rs1333049 presented at an earlier age (62 vs. 63.5 years in non-carriers, P=0.0004) with more extensive disease (number of vessels with significant stenosis: 1.9 vs. 1.7 in non-carriers, P=0.001) in the ACS group. In adjusted models, the C allele was not associated with recurrent MI (hazard ratio [HR], 1.01; 95% confidence interval [CI]: 0.74-1.38), recurrent revascularization (HR, 0.98; 95%CI: 0.78-1.23), or death (HR, 0.91; 95%CI: 0.69-1.18) in the ACS or CABG groups (recurrent MI: HR, 0.64; 95%CI: 0.40-1.05; recurrent revascularization: HR, 0.98; 95%CI: 0.61-1.55; death: HR, 0.89; 95%CI: 0.61-1.30). Results were similar for the other 3 SNPs.
CONCLUSIONS: 9p21 SNPs were not associated with recurrent MI, revascularization, or mortality after ACS or CABG. Individuals with the rs1333049 C allele, however, may present with earlier and more extensive disease.

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Year:  2012        PMID: 22322877      PMCID: PMC3837386          DOI: 10.1253/circj.cj-11-1166

Source DB:  PubMed          Journal:  Circ J        ISSN: 1346-9843            Impact factor:   2.993


  17 in total

1.  Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

Authors:  Gong-Qing Shen; Lin Li; Shaoqi Rao; Kalil G Abdullah; Ji Min Ban; Bok-Soo Lee; Jeong Euy Park; Qing K Wang
Journal:  Arterioscler Thromb Vasc Biol       Date:  2007-11-29       Impact factor: 8.311

2.  Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men.

Authors:  Philippa J Talmud; Jackie A Cooper; Jutta Palmen; Ruth Lovering; Fotios Drenos; Aroon D Hingorani; Steve E Humphries
Journal:  Clin Chem       Date:  2008-02-04       Impact factor: 8.327

3.  Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population.

Authors:  Yumiko Hiura; Yasue Fukushima; Miyuki Yuno; Hiromi Sawamura; Yoshihiro Kokubo; Tomonori Okamura; Hitonobu Tomoike; Yoichi Goto; Hiroshi Nonogi; Rie Takahashi; Naoharu Iwai
Journal:  Circ J       Date:  2008-08       Impact factor: 2.993

4.  No association of chromosome 9p21.3 variation with clinical and angiographic outcomes after placement of drug-eluting stents.

Authors:  Petra Hoppmann; Anna Erl; Serin Türk; Klaus Tiroch; Julinda Mehilli; Albert Schömig; Adnan Kastrati; Werner Koch
Journal:  JACC Cardiovasc Interv       Date:  2009-11       Impact factor: 11.195

5.  Additive effect of ANRIL and BRAP polymorphisms on ankle-brachial index in a Taiwanese population.

Authors:  Pei-Chien Tsai; Yi-Chu Liao; Tsung-Hsien Lin; Edward Hsi; Yi-Hsin Yang; Suh-Hang Hank Juo
Journal:  Circ J       Date:  2011-11-27       Impact factor: 2.993

6.  A common allele on chromosome 9 associated with coronary heart disease.

Authors:  Ruth McPherson; Alexander Pertsemlidis; Nihan Kavaslar; Alexandre Stewart; Robert Roberts; David R Cox; David A Hinds; Len A Pennacchio; Anne Tybjaerg-Hansen; Aaron R Folsom; Eric Boerwinkle; Helen H Hobbs; Jonathan C Cohen
Journal:  Science       Date:  2007-05-03       Impact factor: 47.728

7.  Intensive versus moderate lipid lowering with statins after acute coronary syndromes.

Authors:  Christopher P Cannon; Eugene Braunwald; Carolyn H McCabe; Daniel J Rader; Jean L Rouleau; Rene Belder; Steven V Joyal; Karen A Hill; Marc A Pfeffer; Allan M Skene
Journal:  N Engl J Med       Date:  2004-03-08       Impact factor: 91.245

8.  Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.

Authors:  Heribert Schunkert; Anika Götz; Peter Braund; Ralph McGinnis; David-Alexandre Tregouet; Massimo Mangino; Patrick Linsel-Nitschke; Francois Cambien; Christian Hengstenberg; Klaus Stark; Stefan Blankenberg; Laurence Tiret; Pierre Ducimetiere; Andrew Keniry; Mohammed J R Ghori; Stefan Schreiber; Nour Eddine El Mokhtari; Alistair S Hall; Richard J Dixon; Alison H Goodall; Henrike Liptau; Helen Pollard; Daniel F Schwarz; Ludwig A Hothorn; H-Erich Wichmann; Inke R König; Marcus Fischer; Christa Meisinger; Willem Ouwehand; Panos Deloukas; John R Thompson; Jeanette Erdmann; Andreas Ziegler; Nilesh J Samani
Journal:  Circulation       Date:  2008-03-24       Impact factor: 29.690

9.  Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility.

Authors:  Jeffrey L Anderson; Benjamin D Horne; Matthew J Kolek; Joseph B Muhlestein; Chrissa P Mower; James J Park; Heidi T May; Nicola J Camp; John F Carlquist
Journal:  Am Heart J       Date:  2008-10-11       Impact factor: 4.749

10.  Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in the Atherosclerosis Risk in Communities study.

Authors:  Ariel Brautbar; Christie M Ballantyne; Kim Lawson; Vijay Nambi; Lloyd Chambless; Aaron R Folsom; James T Willerson; Eric Boerwinkle
Journal:  Circ Cardiovasc Genet       Date:  2009-04-21
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  20 in total

1.  A novel genetic marker of decreased inflammation and improved survival after acute myocardial infarction.

Authors:  Edward D Coverstone; Richard G Bach; LiShiun Chen; Laura J Bierut; Allie Y Li; Petra A Lenzini; Heidi C O'Neill; John A Spertus; Carmen C Sucharov; Jerry A Stitzel; Joel D Schilling; Sharon Cresci
Journal:  Basic Res Cardiol       Date:  2018-08-10       Impact factor: 17.165

2.  Effects of Gender-Specific Differences, Inflammatory Response, and Genetic Variation on the Associations Among Depressive Symptoms and the Risk of Major Adverse Coronary Events in Patients With Acute Coronary Syndrome.

Authors:  Jennifer Sanner; Megan L Grove; Erica Yu; F Gerard Moeller; Stanley G Cron; Eric Boerwinkle; Alanna C Morrison; Lorraine Frazier
Journal:  Biol Res Nurs       Date:  2018-01-03       Impact factor: 2.522

3.  Polymorphisms in glutathione S-transferase are risk factors for perioperative acute myocardial infarction after cardiac surgery: a preliminary study.

Authors:  Viktória Kovacs; Balazs Gasz; Borbala Balatonyi; Luca Jaromi; Peter Kisfali; Balazs Borsiczky; Gabor Jancso; Nandor Marczin; Sandor Szabados; Bela Melegh; Alotti Nasri; Elisabeth Roth
Journal:  Mol Cell Biochem       Date:  2014-01-17       Impact factor: 3.396

4.  Single nucleotide polymorphisms in cholesteryl ester transfer protein gene and recurrent coronary heart disease or mortality in patients with established atherosclerosis.

Authors:  Salim S Virani; Vei-Vei Lee; Ariel Brautbar; Megan L Grove; Vijay Nambi; Mahboob Alam; MacArthur Elayda; James M Wilson; James T Willerson; Eric Boerwinkle; Christie M Ballantyne
Journal:  Am J Cardiol       Date:  2013-07-25       Impact factor: 2.778

5.  The cardiovascular implication of single nucleotide polymorphisms of chromosome 9p21 locus among Arab population.

Authors:  Ayman A El-Menyar; Nasser M Rizk; Awad Al-Qahtani; Fahad AlKindi; Ahmed Elyas; Fathi Farag; Fadheela Dad Bakhsh; Samah Ebrahim; Emad Ahmed; Mooza Al-Khinji; Hassan Al-Thani; Jassim Al Suwaidi
Journal:  J Res Med Sci       Date:  2015-04       Impact factor: 1.852

6.  Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery.

Authors:  Miklos D Kertai; Yi-Ju Li; Yen-Wei Li; Yunqi Ji; John Alexander; Mark F Newman; Peter K Smith; Diane Joseph; Joseph P Mathew; Mihai V Podgoreanu
Journal:  BMJ Open       Date:  2015-05-06       Impact factor: 2.692

7.  Genetic Variant rs10757278 on Chromosome 9p21 Contributes to Myocardial Infarction Susceptibility.

Authors:  Guangyuan Chen; Xiuhua Fu; Guangyu Wang; Guiyou Liu; Xiuping Bai
Journal:  Int J Mol Sci       Date:  2015-05-21       Impact factor: 5.923

8.  Genetic variation in Tanis was associated with elevating plasma triglyceride level in Chinese nondiabetic subjects.

Authors:  Ying Gao; Xiang Xie; Yi-Tong Ma; Yi-Ning Yang; Xiao-Mei Li; Zhen-Yan Fu; Ying-Ying Zheng; Xiang Ma; Bang-Dang Chen; Fen Liu; Ying Huang
Journal:  Lipids Health Dis       Date:  2013-07-05       Impact factor: 3.876

9.  Association between 9p21 genetic variants and mortality risk in a prospective cohort of patients with type 2 diabetes (ZODIAC-15).

Authors:  Gijs W D Landman; Jana V van Vliet-Ostaptchouk; Nanne Kleefstra; Kornelis J J van Hateren; Iefke Drion; Klaas H Groenier; Rijk O B Gans; Harold Snieder; Marten H Hofker; Henk J G Bilo
Journal:  Cardiovasc Diabetol       Date:  2012-11-07       Impact factor: 9.951

10.  Association of Myocardial Infarction with CDKN2B Antisense RNA 1 (CDKN2B-AS1) rs1333049 Polymorphism in Slovenian Subjects with Type 2 Diabetes Mellitus.

Authors:  Miha Tibaut; Franjo Naji; Daniel Petrovič
Journal:  Genes (Basel)       Date:  2022-03-16       Impact factor: 4.096

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