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Factor VII, blood lipids and fat intake: gene-nutrient interaction and risk of coronary heart disease with the factor
R Bowman1, A M C P Joosen, A A Welch
1MRC Dunn Human Nutrition Unit, Cambridge, UK.
Insights
Dietary fat intake impacts factor VII coagulant activity (FVIIc) in women, while blood lipids affect FVIIc in both genders. The R353Q gene variant had minimal influence on these associations, though it modified the triacylglycerol-FVIIc link in men.
Area of Science:
- Cardiovascular epidemiology
- Nutritional science
- Human genetics
Background:
- Investigated the relationship between dietary fat, blood lipids, factor VII coagulant activity (FVIIc), and coronary heart disease (CHD) risk.
- Assessed the influence of the factor VII gene R353Q polymorphism on these associations.
Purpose of the Study:
- To determine how dietary fat and blood lipid levels relate to FVIIc.
- To examine the role of the FVII R353Q polymorphism in modulating these relationships and CHD risk.
Main Methods:
- Cross-sectional analysis of 15,073 participants from the EPIC-Norfolk study.
- Nested case-control study including 985 CHD cases and 2009 controls.
- Genotyping for the FVII R353Q polymorphism.
Main Results:
- FVIIc associated with total fat intake in women, particularly RR homozygotes.
- FVIIc positively correlated with total cholesterol and triacylglycerol in both genders.
- The R353Q genotype showed a significant interaction with triacylglycerol levels in males.
- No significant effect of genotype on incident CHD risk was observed.
Conclusions:
- Dietary fat intake is strongly linked to FVIIc in women; serum lipids are linked in both genders.
- The R353Q genotype has a minor impact on dietary fat modulation of FVIIc.
- The association between triacylglycerol and FVIIc is stronger in males carrying the Q allele.
Background:
The relation between dietary fat, blood lipids, plasma factor VII coagulant activity (FVIIc) and risk of coronary heart disease (CHD) according to the R353Q polymorphism in the factor VII gene was assessed.
Methods:
Cross-sectional study of 15,073 individuals participating in the European Prospective Investigation of Cancer (EPIC) Norfolk, 7433 of which had FVIIc available. Nested case-control study of 985 CHD cases and 2009 matched controls.
Results:
FVIIc was significantly associated with total fat intake in females, especially in the RR homozygotes (standardized beta=0.24; 95% confidence interval (95% CI) 0.08-0.40; P<0.01), but there were no associations with intakes of saturated, monounsaturated or polyunsaturated fatty acids according to genotype and no associations in males. FVIIc was significantly positively associated with total cholesterol (P<0.01) and with triacylglycerol (P<0.001) in both genders, with an interaction according to genotype for triacylglycerol in males: beta Q allele carriers 0.26 (95% CI 0.18-0.34), beta RR homozygotes 0.16 (95% CI 0.12-0.20) (Z interaction=-2.24; P<0.05). There was no effect of genotype on the odds ratio (OR) for incident CHD: OR 0.89 for Q allele carriers compared with RR homozygotes (95% CI 0.77-1.02) in 985 cases and 2009 matched controls.
Conclusion:
These results show a strong association between dietary fat intake and FVIIc in women, and between serum triacylglycerol and cholesterol and FVIIc levels in both genders. The R353Q genotype only marginally affected modulation of FVIIc by dietary fat. The association between triacylglycerol and FVIIc was significantly stronger in males carrying the Q allele than in those with the RR genotype.
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