New variants in the apolipoprotein AV gene in individuals with extreme triglyceride levels
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
15046561
Knihovny.cz E-resources
- MeSH
- Apolipoprotein A-V MeSH
- Apolipoproteins A MeSH
- Apolipoproteins genetics MeSH
- Cholesterol blood MeSH
- Adult MeSH
- Gene Frequency genetics MeSH
- Genotype MeSH
- Middle Aged MeSH
- Humans MeSH
- Mutation, Missense * MeSH
- Polymorphism, Genetic MeSH
- Triglycerides 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
- APOA5 protein, human MeSH Browser
- Apolipoprotein A-V MeSH
- Apolipoproteins A MeSH
- Apolipoproteins MeSH
- Cholesterol MeSH
- Triglycerides MeSH
Animal studies (on transgenic and knock-out mice) and human association analysis assessed the importance of APOAV gene for plasma triglyceride determination. New APOAV missense variants (Val153 --> Met and Cys185 --> Gly) have been detected recently. We have analyzed these variants in 83 unrelated patients with extreme lipid parameters (triglycerides of 20.4+/-2.8 mmol/l and total cholesterol of 10.4+/-3.7 mmol/l) and in a control population group consisting of 2,559 unrelated Caucasians. In patients, the frequency of the Met153 carriers was slightly but not significantly higher (9.64 % vs. 6.49 %) compared to the population sample. This suggested that Val153 Met polymorphism in the APOAV gene does not represent an important risk factor for developing the extreme levels of plasma triglycerides. We did not detect carriers of the Gly185 allele among patients or 420 healthy individuals. We suppose that this variant is probably not present in Caucasian populations
APOAV (T-1131>C) variant has no effect on mother's height in a large population study