Postprandial response of activated factor VII in elderly women depends on the R353Q polymorphism

Am J Clin Nutr. 1999 Oct;70(4):435-8. doi: 10.1093/ajcn/70.4.435.

Abstract

Background: Activated factor VII (FVIIa) is a very potent coagulant and may be a key determinant of the outcome of a cardiovascular event. The main determinants of FVIIa are the R353Q polymorphism and dietary fat intake, which may have an interactive effect.

Objective: The objective was to investigate whether the response of FVIIa to a fat-rich breakfast varies across genotypes of the R353Q polymorphism.

Design: Ninety-one apparently healthy elderly women (>60 y of age), 56 with the RR genotype and 35 with the RQ or QQ genotype, participated in a randomized, controlled crossover study. Subjects received 5 breakfasts, each on a separate day: 1 low-fat control breakfast and 4 high-fat test breakfasts. Blood samples were taken for measurement of FVIIa at 0800 before each breakfast (fasting) and at 1300 and 1500.

Results: The mean (+/-SD) fasting FVIIa concentration was 93.3 +/- 26.7 U/L in women with the RR genotype, 49.3 +/- 19.1 U/L in those with the RQ genotype and 39.5 +/- 17.2 U/L in those with the QQ genotype. The mean absolute response to all 4 test breakfasts was 37.0 U/L in those with the RR genotype and 16. 1 U/L in those carrying the Q allele (P < 0.001 for difference). Likewise, the FVIIa response relative to fasting FVIIa was significantly higher in women homozygous for the R allele.

Conclusion: This observation may indicate a considerable difference in cardiovascular risk between genotype groups as a result of an increase in FVIIa after a fat-rich diet.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Cross-Over Studies
  • DNA / chemistry
  • Dietary Fats / administration & dosage
  • Dietary Fats / metabolism*
  • Factor VIIa / analysis
  • Factor VIIa / genetics
  • Factor VIIa / physiology*
  • Female
  • Genotype
  • Humans
  • Polymerase Chain Reaction
  • Polymorphism, Genetic / genetics*
  • Postprandial Period / physiology*
  • Regression Analysis

Substances

  • Dietary Fats
  • DNA
  • Factor VIIa