The purpose of this study is to determine whether supplementation with 5 mg vitamin K daily over a 2-year period will prevent bone loss in post-menopausal women with osteopenia.
Osteoporosis is major cause of morbidity and mortality in Canadian postmenopausal women. It is a systemic disease characterized by low bone mass and deterioration of bone microarchitecture, resulting in bone fragility and an increased risk of fractures. One in six women over the age of 50 have osteoporosis. The lifetime risk of an osteoporotic fracture for an average 50 year-old Canadian woman is \>40%. The annual health care costs for osteoporotic fractures in Canada have been estimated to exceed $1.3 billion. Recent data suggest that vitamin K supplements may decrease bone loss and prevent fractures. Vitamin K is a co-factor of gamma-glutamyl carboxylase, an enzyme that catalyzes the gamma-carboxylation of glutamic acid residues in bone matrix proteins such as osteocalcin. Vitamin K has been reported to enhance bone formation in both in vitro studies and in vivo studies in animals. Vitamin K levels are low in individuals with osteoporosis and in patients with osteoporotic fractures. The few studies examining vitamin K supplementation in humans have showed promising results with no significant side effects, but these studies had significant methodological shortcomings such as inadequate sample size and lack of randomization. The primary objective of our study is to examine whether vitamin K supplementation will increase bone mineral density in postmenopausal women with osteopenia. Our secondary objectives are to examine the possible adverse effects from long-term vitamin K supplementation, to investigate whether vitamin K will decrease risk of fractures and to determine if vitamin K affects quality of life. Our hypotheses are that vitamin K increases bone mineral density in postmenopausal women, and that there are no significant adverse effects from vitamin K supplementation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
440
1 pill daily
St. Michael's Hospital Health Centre
Toronto, Ontario, Canada
Mt. Sinai Hospital
Toronto, Ontario, Canada
University Health Network, Osteoporosis Department
Toronto, Ontario, Canada
Sunnybrook & Women's College Health Sciences Centre
Toronto, Ontario, Canada
Percent Change in Bone Mineral Density (BMD) at the Lumbar Spine (L1-L4) Between Treatment Arms.
BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer
Time frame: 0 to 24 months
Percent Change in Bone Mineral Density (BMD) at the Total Hip Between Treatment Arms.
BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer
Time frame: 0 to 24 months
Percent Change in Bone Mineral Density (BMD) at the Femoral Neck Between Treatment Arms.
BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer
Time frame: 0 to 24 months
Percent Change in Bone Mineral Density (BMD) at the Ultra-distal Radius Between Treatment Arms.
BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer
Time frame: 0 to 24 months
Effect of Vitamin K1 Supplementation on Levels of Bone Formation Marker
measured by osteocalcin on elecsys platform
Time frame: 0-24 months
Effect of Vitamin K1 Supplementation on Level of Bone Resorption Markers (C-telopeptide: CTX)
measured by CTX Elisa assay on elecsys platform
Time frame: 0-24 months
Effect of Vitamin K1 Supplementation on Percent of Carboxylation of Osteocalcin
measured by osteocalcin hydroxyapatite binding assay
Time frame: 0 to 24 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
University of Toronto
Toronto, Ontario, Canada
Percent Change in Bone Mineral Density (BMD) at the Total Hip Between Treatment Arms.
BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer
Time frame: 0 to 48 months
Percent Change in Bone Mineral Density (BMD) at the Lumbar Spine (L1-L4) Between Treatment Arms.
BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer
Time frame: 0 to 48 months
Percent Change in Bone Mineral Density (BMD) at the Femoral Neck Between Treatment Arms.
BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer
Time frame: 0 to 48 months
Percent Change in Bone Mineral Density (BMD) at the Ultra-distal Radius Between Treatment Arms.
BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer
Time frame: 0 to 48 months
Difference in Serious Adverse Events
These include hospitalizations for pneumonia, heart failure, gastro-intestinal bleeding, elective and non-elective surgery, cancer and death.
Time frame: up to 48 months
Difference in Number of New Cancers by Treatment Arm.
Time frame: up to 48 months
Difference in Number of New Clinical Fractures by Treatment Arm.
these included fragility fractures
Time frame: up to 48 months