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

Citation
Li. Mennen et al., Postprandial response of activated factor VII in elderly women depends an the R353Q polymorphism, AM J CLIN N, 70(4), 1999, pp. 435-438
Citations number
18
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
AMERICAN JOURNAL OF CLINICAL NUTRITION
ISSN journal
00029165 → ACNP
Volume
70
Issue
4
Year of publication
1999
Pages
435 - 438
Database
ISI
SICI code
0002-9165(199910)70:4<435:PROAFV>2.0.ZU;2-2
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 de terminants of FVIIa are the R353Q polymorphism and dietary fat intake, whic h may have an interactive effect. Objective: The objective was to investigate whether the response of FVIIa t o 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 rando mized, 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 brea kfast (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 Re geno type and 39.5 +/- 17.2 U/L in those with the ee genotype. The mean absolute response to all 4 test breakfasts was 37.0 U/L in those with the RR genoty pe 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 hi gher in women homozygous for the R allele. Conclusion: This observation may indicate a considerable difference in card iovascular risk between genotype groups as a result of an increase in FVIIa after a fat-rich diet.