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Does 24R,25(OH)2-vitamin D3 prevent postmenopausal bone loss?

B J Riis, K Thomsen, C Christiansen

    Calcified Tissue International
    |September 1, 1986
    PubMed
    Summary

    Oral 24R,25(OH)2-vitamin D3 did not prevent postmenopausal bone loss in a 2-year trial. This vitamin D3 treatment showed no prophylactic effect on bone mineral density or calcium metabolism in early postmenopausal women.

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    Area of Science:

    • Endocrinology
    • Metabolic Bone Disease
    • Nutritional Science

    Background:

    • Postmenopausal bone loss is a significant health concern.
    • Vitamin D metabolites are crucial for calcium homeostasis and bone health.
    • The role of 24R,25(OH)2-vitamin D3 in preventing bone loss requires further investigation.

    Purpose of the Study:

    • To evaluate the efficacy of oral 24R,25(OH)2-vitamin D3 as a prophylactic agent against postmenopausal bone loss.
    • To assess the impact of 24R,25(OH)2-vitamin D3 on calcium metabolic variables in postmenopausal women.

    Main Methods:

    • A 2-year, double-blind, placebo-controlled therapeutic trial involving 58 healthy, early postmenopausal women.
    • Randomization to daily 10 microgram 24R,25(OH)2D3 or placebo.
    • Regular monitoring of bone mineral density (forearm, lumbar spine, total body) and calcium metabolic markers (serum calcium, alkaline phosphatase, urinary hydroxyproline, radiocalcium absorption).

    Main Results:

    • No significant difference in the rate of bone mineral loss was observed between the 24R,25(OH)2-vitamin D3 and placebo groups.
    • Forearm, lumbar spine, and total body bone mineral content decreased significantly and similarly in both treatment arms.
    • Serum calcium, alkaline phosphatase, fasting urinary hydroxyproline, 24-hour urinary calcium excretion, and radiocalcium absorption remained unchanged in both groups.

    Conclusions:

    • Oral 24R,25(OH)2-vitamin D3 administration does not offer a prophylactic effect against postmenopausal bone loss.
    • The treatment did not influence key calcium metabolic variables in the studied population.
    • Further research may be needed to explore other vitamin D metabolites or therapeutic strategies for postmenopausal osteoporosis.

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