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MMP1 and MMP3 gene polymorphisms in patients with acute coronary syndromes
Andrzej Pawlik1, Marzenna Plucinska2, Mikołaj Kopec1
1Department of Physiology, Pomeranian Medical University, Szczecin, Poland.
Abstract:
Matrix metalloproteinases (MMPs) are the group of proteolytic enzymes that break down the components of the connective tissue matrix leading to unstable atherosclerotic plaques. The aim of this study was to examine the association between MMP1-1607dupG (rs1799750) and MMP3-1171dupA (rs3025058) gene polymorphisms and acute coronary syndromes (ACS) in the form of unstable angina. This study included 197 patients with ACS in the form of unstable angina confirmed by coronary angiography (defined by >70% stenosis in at least one major coronary artery) and 144 healthy controls. There was no statistically significant difference in the distribution of the MMP1-1607dupG (rs1799750) polymorphism between patients with unstable angina and the control group. With regard to the MMP3-1171dupA (rs3025058) polymorphism, a significant increase in the frequency of the 6A/6A genotype among patients with unstable angina was detected. This association was confirmed in multivariate logistic regression analysis, where male sex and rs3025058 6A/6A genotype were significantly associated with an increased risk of ACS. © 2017 IUBMB Life, 69(11):850-855, 2017.
Insights
The MMP3-1171dupA gene variant (rs3025058) 6A/6A genotype is linked to a higher risk of acute coronary syndromes (ACS), specifically unstable angina. No significant association was found for the MMP1-1607dupG polymorphism.
Area of Science:
- Cardiovascular Genetics
- Molecular Biology
- Biochemistry
Background:
- Matrix metalloproteinases (MMPs) degrade connective tissue, contributing to unstable atherosclerotic plaques.
- Genetic variations in MMPs may influence susceptibility to cardiovascular diseases like acute coronary syndromes (ACS).
Purpose of the Study:
- To investigate the association between specific gene polymorphisms in MMP1 (rs1799750) and MMP3 (rs3025058) and the risk of ACS presenting as unstable angina.
Main Methods:
- Case-control study involving 197 patients with unstable angina and 144 healthy controls.
- Genotyping for MMP1-1607dupG (rs1799750) and MMP3-1171dupA (rs3025058) polymorphisms using coronary angiography for diagnosis.
- Statistical analysis, including multivariate logistic regression, to determine associations.
Main Results:
- No significant difference in MMP1-1607dupG (rs1799750) polymorphism distribution between patients and controls.
- A significantly higher frequency of the MMP3-1171dupA (rs3025058) 6A/6A genotype was observed in unstable angina patients compared to controls.
- Male sex and the rs3025058 6A/6A genotype were independently associated with an increased risk of ACS.
Conclusions:
- The MMP3-1171dupA (rs3025058) 6A/6A genotype is a potential genetic risk factor for developing acute coronary syndromes (unstable angina).
- MMP1 gene polymorphism (rs1799750) does not appear to be associated with unstable angina in this population.
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