Title of article :
Genotypes associated with myocardial infarction risk are more common in African Americans than in European Americans Original Research Article
Author/Authors :
David E. Lanfear، نويسنده , , Sharon Marsh، نويسنده , , Sharon Cresci، نويسنده , , William D. Shannon، نويسنده , , John A. Spertus، نويسنده , , Howard L. McLeod، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
3
From page :
165
To page :
167
Abstract :
Objectives This study was designed to describe the frequencies of multiple myocardial infarction (MI) risk-associated genotypes among different racial groups. Background Racial disparities in the prevalence of cardiovascular disease (CVD) are well known. Recent large Japanese case-control studies identified connexin-37 (GJA-4), plasminogen activator inhibitor-1 (PAI-1), and stromelysin-1 (MMP-3) polymorphisms as risk factors for MI, but the prevalence of these genotypes among different racial groups in the U.S. needs to be determined. Methods Genomic deoxyribonucleic acid from 95 healthy African Americans (AA) and 95 healthy European Americans (EA) was used for genotyping. Deoxyribonucleic acid containing the region of interest was amplified using the polymerase chain reaction, followed by genotyping using pyrosequencing. Results All three MI-risk genotypes were observed in both populations and were in Hardy-Weinberg equilibrium. The frequencies of two of the three “risk-associated” genotypes were significantly higher in the AA population: GJA4 C1019T T/T: AA, 20%, EA, 7% (p = 0.053); MMP3 −1171delA A/A: AA, 78%, EA, 24% (p < 0.001); PAI-1 −668delG G/G: AA, 55%, EA, 16% (p < 0.001). The likelihood of two or more high-risk genotypes was 3.3% among EA subjects and 51% in the AA group (p < 0.001). We found that 9.1% of AA had all three high-risk genotypes, compared with 0% among the EA group (p = 0.0097). Conclusions We found higher frequencies of disease-associated genotypes in AA than in EA. Our results also show that more AA than EA carry multiple risk-associated genotypes. Future studies need to assess whether such genetic profiles predict adverse outcomes in U.S. populations and contribute to racial disparities in CVD burden.
Keywords :
AA , myocardial infarction , polymerase chain reaction , DNA , deoxyribonucleic acid , PCR , cardiovascular disease , PAI-1 , coronary heart disease , African Americans , MMP-3 , SNP , Single nucleotide polymorphism , MI , CVD , CHD , Ea , European Americans , GJA-4 , connexin-37 , stromelysin-1 , plasminogen activator inhibitor-1
Journal title :
JACC (Journal of the American College of Cardiology)
Serial Year :
2004
Journal title :
JACC (Journal of the American College of Cardiology)
Record number :
459244
Link To Document :
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