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The additive effect of vitamin K supplementation and bisphosphonate on fracture risk in post-menopausal osteoporosis: a randomised placebo controlled trial.

Archives of osteoporosis
January 1, 1970
Amelia E Moore et al. (10 authors)
Randomized Controlled TrialJournal ArticleResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to determine whether vitamin K supplementation, when combined with calcium and/or vitamin D and bisphosphonate, had an additive effect on bone mineral density and fracture risk in post-menopausal women with osteoporosis.

Results Summary

The study found no significant differences in bone mineral density or bone turnover markers between groups receiving vitamin K supplementation and those not receiving it, suggesting no additive effect of vitamin K when combined with calcium and/or vitamin D and bisphosphonate.

Population

Post-menopausal women with osteoporosis and sub-optimal vitamin K status (average age 68.7 years).

Effective Dosage

Not specified

Duration

Not specified

Interactions

Bisphosphonate, vitamin D

Extracted Claims (7)
InterventionDirectionEndpointPopulationDosageImpactClaim #
vitamin K, given with oral bisphosphonate, calcium and/or vitamin D
decrease
fracture risk
post-menopausal women with osteoporosis
-
has an additive effect
#1
vitamin K
no change
bone density or bone turnover
post-menopausal women with osteoporosis
-
No difference
#2
vitamin K
decrease
bone loss
-
-
prevents
#3
vitamin K
decrease
fracture risk
-
-
may improve
#4
vitamin K supplementation
increase
bone mineral density (BMD), hip geometry and bone turnover markers (BTMs)
post-menopausal women with osteoporosis (PMO) and sub-optimum vitamin K status receiving bisphosphonate, calcium and/or vitamin D treatment
-
has an additive effect
#5
vitamin K
no change
BMD at the total hip, femoral neck and lumbar spine and BTMs; CTX and P1NP
105 women aged 68.7[12.3] years with PMO and serum vitamin K
-
did not differ significantly
#6
vitamin K
no change
BMD at the total hip, femoral neck and lumbar spine and BTMs; CTX and P1NP
105 women aged 68.7[12.3] years with PMO and serum vitamin K
-
did not differ significantly
#7
Abstract

UNLABELLED: This study assessed whether vitamin K, given with oral bisphosphonate, calcium and/or vitamin D has an additive effect on fracture risk in post-menopausal women with osteoporosis. No difference in bone density or bone turnover was observed although vitamin K PURPOSE: Some clinical studies have suggested that vitamin K prevents bone loss and may improve fracture risk. The aim was to assess whether vitamin K supplementation has an additive effect on bone mineral density (BMD), hip geometry and bone turnover markers (BTMs) in post-menopausal women with osteoporosis (PMO) and sub-optimum vitamin K status receiving bisphosphonate, calcium and/or vitamin D treatment. METHODS: We conducted a trial in 105 women aged 68.7[12.3] years with PMO and serum vitamin K RESULTS: Changes in BMD at the total hip, femoral neck and lumbar spine and BTMs; CTX and P1NP did not differ significantly following either K CONCLUSION: The addition of vitamin K TRIAL REGISTRATION: The study was registered at Clinicaltrial.gov:NCT01232647.

Medical Subject Headings (MeSH)
FemaleHumansOsteoporosis, PostmenopausalVitamin KDiphosphonatesCalciumFractures, BoneBone DensityVitaminsVitamin DVitamin K 1Femur NeckCalcium, DietaryDietary Supplements
Study Links
Quality Scores
SafetyNot Assessed
Efficacy50/10
Quality75/10
Citation Metrics
Total Citations9
Citations/Year4.5
Relative Citation Ratio2.56
NIH Percentile81.3%
Research Impact Scores
APT Score0.75
Weight Score1.58
Normalized Score0.55
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