Inflammation Clinical Trial
Official title:
Effect of Vitamin K on Age-Related Bone Loss and Vascular Calcification
The purpose of this study is to determine if supplemental vitamin K will reduce age-related bone loss in elderly men and women above that achieved by supplementation.
This is a three-year, double-blind, placebo-controlled trial to study the effect of vitamin
K supplementation (500 µg/d) on bone density at the hip, markers of bone turnover, vascular
calcification, osteoarthritis and tests of concentration in 452 men and women, aged 60-80
years. All participants will also be receiving calcium and vitamin D supplements, in
addition to a multivitamin, to prevent any potential bone loss associated with dietary
inadequacy of these nutrients.
Measurements of plasma vitamin K concentrations, percent undercarboxylated osteocalcin
(markers of vitamin K status), serum osteocalcin, collagen Type-I-crosslink N-telopeptides
(markers of bone turnover) and BMD of the hip, as well as the heel, spine and total body at
0, 6, 12, 24, and 36 months of vitamin K supplementation. Vascular calcification will be
measured at baseline and at 36 months of vitamin K supplementation by multi-slice CT scan.
An additional EKG will be performed at 36 months of vitamin K supplementation to determine
cardiac changes that may have occurred over the course of the study. Bilateral hand x-rays
will be measured at 36 months of vitamin K supplementation, as will the administration of
the Framingham OA questionnaire. Plasma 25-hydroxyvitamin D concentrations and urinary
calcium and sodium will be measured at the same time points to be used as covariates in this
assessment. In addition, 1,25-dihydroxyvitamin D will be measured at the beginning and end
of the study. Other covariates collected throughout the study include age, weight,
anthropometric data, physical activity, medication used, smoking, plasma lipids, insulin and
measures of inflammation, B vitamins and dietary intakes. In addition, two tests of
attention and concentration will be administered at 36 months of vitamin K supplementation.
This trial will determine if supplemental vitamin K will reduce age-related bone loss,
vascular calcification, osteoarthritis and concentration in elderly men and women, above
that achieved by supplemental calcium and vitamin D alone.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
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