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Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction

Authors :
Massachusetts Institute of Technology. Department of Biology
Altshuler, David
Ardissino, Diego
Berzuini, Carlo
Merlini, Piera Angelica
Mannuccio Mannucci, Pier
Surti, Aarti
Burtt, Noel
Voight, Benjamin
Tubaro, Marco
Peyvandi, Flora
Spreafico, Marta
Celli, Patrizia
Lina, Daniela
Notarangelo, Maria Francesca
Ferrario, Maurizio
Fetiveau, Raffaela
Casari, Giorgio
Galli, Michele
Ribichini, Flavio
Rossi, Marco L.
Bernardi, Francesco
Marziliano, Nicola
Zonzin, Pietro
Mauri, Francesco
Piazza, Alberto
Foco, Luisa
Bernardinelli, Luisa
Kathiresan, Sekar
Massachusetts Institute of Technology. Department of Biology
Altshuler, David
Ardissino, Diego
Berzuini, Carlo
Merlini, Piera Angelica
Mannuccio Mannucci, Pier
Surti, Aarti
Burtt, Noel
Voight, Benjamin
Tubaro, Marco
Peyvandi, Flora
Spreafico, Marta
Celli, Patrizia
Lina, Daniela
Notarangelo, Maria Francesca
Ferrario, Maurizio
Fetiveau, Raffaela
Casari, Giorgio
Galli, Michele
Ribichini, Flavio
Rossi, Marco L.
Bernardi, Francesco
Marziliano, Nicola
Zonzin, Pietro
Mauri, Francesco
Piazza, Alberto
Foco, Luisa
Bernardinelli, Luisa
Kathiresan, Sekar
Source :
Elsevier
Publication Year :
2014

Abstract

Objectives: The purpose of this study was to test whether the 9p21.3 variant rs1333040 influences the occurrence of new cardiovascular events and coronary atherosclerosis progression after early-onset myocardial infarction. Background: 9p21.3 genetic variants are associated with ischemic heart disease, but it is not known whether they influence prognosis after an acute coronary event. Methods: Within the Italian Genetic Study of Early-onset Myocardial Infarction, we genotyped rs1333040 in 1,508 patients hospitalized for a first myocardial infarction before the age of 45 years who underwent coronary angiography without index event coronary revascularization. They were followed up for major cardiovascular events and angiographic coronary atherosclerosis progression. Results: Over 16,599 person-years, there were 683 cardiovascular events and 492 primary endpoints: 77 cardiovascular deaths, 223 reoccurrences of myocardial infarction, and 383 coronary artery revascularizations. The rs1333040 genotype had a significant influence (p = 0.01) on the primary endpoint, with an adjusted hazard ratio of 1.19 (95% confidence interval [CI]: 1.08 to 1.37) for heterozygous carriers and 1.41 (95% CI: 1.06 to 1.87) for homozygous carriers. Analysis of the individual components of the primary endpoints provided no significant evidence that the rs1333040 genotype influenced the hazard of cardiovascular death (p = 0.24) or the reoccurrence of myocardial infarction (p = 0.57), but did provide significant evidence that it influenced on the hazard of coronary revascularization, with adjusted heterozygous and homozygous ratios of 1.38 (95% CI: 1.17 to 1.63) and 1.90 (95% CI: 1.36 to 2.65) (p = 0.00015), respectively. It also significantly influenced the angiographic endpoint of coronary atherosclerosis progression (p = 0.002). Conclusions: In early-onset myocardial infarction, the 9p21.3 variant rs1333040 affects the progression of coronary atherosclerosis and the probability of coronary art

Details

Database :
OAIster
Journal :
Elsevier
Notes :
application/pdf, en_US
Publication Type :
Electronic Resource
Accession number :
edsoai.on1141874927
Document Type :
Electronic Resource