Polymorphisms in CYP-7A1, not APOE, influence the change in plasma lipids in response to population dietary change in an 8 year follow-up; results from the Czech MONICA study
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
12810154
DOI
10.1016/s0009-9120(03)00025-0
PII: S0009912003000250
Knihovny.cz E-resources
- MeSH
- Apolipoprotein E2 MeSH
- Apolipoprotein E3 MeSH
- Apolipoprotein E4 MeSH
- Apolipoproteins B blood MeSH
- Apolipoproteins E genetics MeSH
- Cholesterol 7-alpha-Hydroxylase genetics MeSH
- Cholesterol blood MeSH
- Diet Surveys MeSH
- Diet * MeSH
- Adult MeSH
- Genotype MeSH
- Cholesterol, HDL blood MeSH
- Cholesterol, LDL blood MeSH
- Middle Aged MeSH
- Humans MeSH
- Lipids blood MeSH
- Follow-Up Studies MeSH
- Polymorphism, Genetic MeSH
- Aged MeSH
- Triglycerides blood MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- Apolipoprotein E2 MeSH
- Apolipoprotein E3 MeSH
- Apolipoprotein E4 MeSH
- Apolipoproteins B MeSH
- Apolipoproteins E MeSH
- Cholesterol 7-alpha-Hydroxylase MeSH
- Cholesterol MeSH
- Cholesterol, HDL MeSH
- Cholesterol, LDL MeSH
- Lipids MeSH
- Triglycerides MeSH
OBJECTIVES: To evaluate the influence of variation in the genes for apolipoprotein E (APOE; epsilon2, epsilon3, epsilon4) and cholesterol-7alpha hydroxylase (CYP-7A1; -204A-->C) on plasma lipid level changes. DESIGN AND METHODS: 131 males for whom dietary composition markedly changed and total cholesterol decreased (from 6.21 +/- 1.31 mmol/L in 1988 - 5.43 +/- 1.06 mmol/L in 1996) over an 8 yr follow-up study. Polymorphisms were investigated using PCR. RESULTS: APOE genotype influenced plasma total and LDL cholesterol, with carriers of the epsilon4 having the highest and epsilon2 carriers the lowest levels, this reached borderline significance for cholesterol in 1988 (p = 0.06) and strongly affected the 1996 levels of LDL cholesterol (p = 0.008). However, APOE did not influence the change in these measures over time. In contrast, the CYP-7A1 -204A-->C polymorphism did not affect lipid measures per se but was strongly associated with a decrease in plasma total cholesterol [AA -0.38 (+/- 0.20) mmol/L, AC -0.65 +/- (0.08), CC -1.33 (+/- 0.3) mmol/L, p = 0.01] over the 8 yr time period. CONCLUSIONS: Variation in the CYP-7A1 gene may play an important role in an individual's sensitivity to dietary composition.
References provided by Crossref.org
Cholesterol associated genetic risk score and acute coronary syndrome in Czech males
Genetics of Familial Hypercholesterolemia: New Insights