The influence of apolipoprotein A5 T-1131C and apolipoprotein E common genetic variants on the levels of hemostatic markers in dyslipidemic patients
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24815086
DOI
10.1016/j.cca.2014.04.029
PII: S0009-8981(14)00206-X
Knihovny.cz E-resources
- Keywords
- Apolipoprotein A5, Apolipoprotein E, Dyslipidemia, Genetic polymorphism, Metabolic syndrome, Tissue plasminogen activator,
- MeSH
- Apolipoproteins A genetics MeSH
- Apolipoproteins E genetics MeSH
- Asymptomatic Diseases MeSH
- Biomarkers blood MeSH
- Adult MeSH
- Dyslipidemias blood genetics physiopathology MeSH
- Hemostasis * MeSH
- Polymorphism, Single Nucleotide * MeSH
- Middle Aged MeSH
- Humans MeSH
- Tissue Plasminogen Activator blood MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Apolipoproteins A MeSH
- Apolipoproteins E MeSH
- Biomarkers MeSH
- Tissue Plasminogen Activator MeSH
OBJECTIVES: The aim of this study was to evaluate the relationships of the T-1131C (rs662799) polymorphism variants of apolipoprotein A5 (Apo A5) gene and variants of apolipoprotein E (Apo E) gene common polymorphism (rs429358, rs7412) to selected hemostatic markers. STUDY DESIGN AND METHODS: We examined 590 asymptomatic dyslipidemic patients, subsequently divided into MetS+ (n=146) and MetS- (n=444) groups according to the criteria for identification of the metabolic syndrome (MetS). We compared variant frequencies and differences in levels of hemostatic markers according to Apo A5, Apo E and Apo A5/Apo E common variants. RESULTS: The -1131C Apo A5 minor variant was associated with elevated tissue plasminogen activator (tPA) in comparison to TT genotype (p<0.001), but not in the MetS+ group. The analysis of Apo A5/Apo E common variants in all subjects revealed that the presence of -1131C minor allele has always been associated with higher levels of tPA in comparison with T allele, regardless of Apo E genotype. Also the presence of minor Apo E2 allele led to elevated tPA concentrations in both T and C carriers. In addition, common -1131C/E2 variant was associated with the highest tPA levels. CONCLUSION: We demonstrated a remarkable association especially between the -1131C Apo A5 variant and increased tPA levels in asymptomatic dyslipidemic patients.
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