The Relationship between Platelet Glycoprotein III a Polymorphism and Acute Coronary Syndrome in Koreans.
10.4070/kcj.1998.28.5.723
- Author:
Kwang Il KIM
;
In Ho CHAE
;
Hyo Soo KIM
;
Dae Won SOHN
;
Byung Hee OH
;
Myoung Mook LEE
;
Young Bae PARK
;
Yun Shik CHOI
;
Young Woo LEE
- Publication Type:Original Article
- Keywords:
Platelet glycoprotein IIIa;
Polymorphism
- MeSH:
Acute Coronary Syndrome*;
Angina, Unstable;
Blood Platelets*;
Coronary Angiography;
DNA;
Electrophoresis;
Fibrinogen;
Gene Frequency;
Genes, vif;
Genotype;
Glycoproteins*;
Heterozygote;
Homozygote;
Humans;
Integrin beta3;
Myocardial Infarction;
Platelet Aggregation;
Polymerase Chain Reaction;
Polymorphism, Restriction Fragment Length;
Risk Factors
- From:Korean Circulation Journal
1998;28(5):723-729
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Platelet plays an important role in the pathogenesis of acute coronary syndrome. Platelet glycoprotein IIb III a is the receptor for fibrinogen, and it plays an important role in the platelet aggregation. It was reported that polymorphism of the platelet glycoprotein III a (PlA1/A2) is related to acute coronary syndrome, especially in young patients. The aims of this study is to evaluate the relationship between platelet glycoprotein III a polymorphism and acute coronary syndrome in Koreans. METHOD: We studied total 208 patients (M: F=131 : 77, mean ages : 57.2+/-9.7). Acute coronary group comprised 110 patients, who underwent coronary angiography with the impression of acute myocardial infarction or unstable angina. Normal group comprised 98 patients who had no significant angiographic lesion. Genomic DNA was extracted from peripheral blood. To determine the frequency of PlA1/A2 genotype, polymerase chain reaction (PCR) was done and the product was restricted with Msp I. 3% gel electrophoresis showed Restriction Fragment Length Polymorphism (RFLP). Clinical profile and risk factor were also reviewed. RESULT: One patient in the acute coronary group is PlA1/A2 heterozygote and all the other are PlA1 homozygote. In normal group, all patients are PlA1 homozygote. The genotypic frequency of PlA1/A2 is consistent with the previous study. CONCLUSION: The genotype frequency of platelet glycoprotein III a gene polymorphism in Koreans is different from that of Caucasian. The allele frequencies of platelet glycoprotein III a is not different between acute coronary syndrome patient and normal control group. Platelet glycoprotein III a polymorphism may not be an hereditary risk factor in Koreans.
