Vitamin K-dependent proteins, including matrix Gla-protein, have been
shown to inhibit vascular calcification. Activation of these proteins via
carboxylation depends on the availability of vitamin K. We examined
whether dietary intake of phylloquinone (vitamin K-1) and menaquinone
(vitamin K-2) were related to aortic calcification and coronary heart
disease (CHD) in the population-based Rotterdam Study. The analysis
included 4807 subjects with dietary data and no history of myocardial
infarction at baseline (1990-1993) who were followed until January 1,
2000. The risk of incident CHD, all-cause mortality, and aortic
atherosclerosis was studied in tertiles of energy-adjusted vitamin K
intake after adjustment for age, gender, BMI, smoking, diabetes,
education, and dietary factors. The relative risk (RR) of CHD mortality
was reduced in the mid and upper tertiles of dietary menaquinone compared
to the lower tertile [RR = 0.73 (95% CI: 0.45, 1.17) and 0.43 (0.24,
0.77), respectively]. Intake of menaquinone was also inversely related to
all-cause mortality [RR = 0.91 (0.75, 1.09) and 0.74 (0.59, 0.92),
respectively] and severe aortic calcification [odds ratio of 0.71 (0.50,
1.00) and 0.48 (0.32, 0.71), respectively]. Phylloquinone intake was not
related to any of the outcomes. These findings suggest tha