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Title:
The effect of high-dose vitamin D on bone mineral density and bone turnover markers in postmenopausal women with low bone massâa randomized controlled 1-year trial | Osteoporosis International
Description:
Vitamin D is widely used in osteoporosis treatment, although the optimal dose is not known. This 1-year clinical study among 297 women aged 50â80 years old showed that a vitamin D3 dose of 6,500 IU/day was not better than the standard dose of 800 IU/day in improving bone mineral density (BMD) in the hip and spine. The purpose of this study was to determine whether a high dose of vitamin D3 was better than the standard dose in improving BMD and reducing bone turnover in postmenopausal women with reduced bone mass. The study was a 1-year randomized double-blind controlled trial comparing high-dose vitamin D3 with the standard dose. Postmenopausal women (nâ=â297) with a BMD T-scoreââ¤ââ2.0 in either lumbar spine (L2â4) or total hip were included and randomized to 6,500 IU vitamin D3/day (20,000 IU twice per weekâ+â800 IU/day) or 800 IU vitamin D3/day (placebo twice per weekâ+â800 IU/day). Both groups were given 1,000 mg elemental calcium/day. The primary endpoint was a change in BMD in total hip and lumbar spine (L2â4). After 1 year, serum 25-hydroxyvitamin D (25(OH)D) increased [mean (SD)] from 71 (23) to 185 (34)ânmol/l and from 71 (22) to 89 (17)ânmol/l in the high- and standard-dose vitamin D groups, respectively. BMD at all measurement sites was unchanged or slightly improved with no significant differences between the groups. Although bone turnover was reduced in both groups, the more pronounced reduction in serum levels of the bone formation marker P1NP in the standard-dose group may indicate that this treatment was more efficient. Adverse events did not differ between the groups. One year treatment with 6,500 IU vitamin D3/day was not better than 800 IU/day regarding BMD in vitamin D-replete postmenopausal women with reduced bone mass and was less efficient in reducing bone turnover.
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randomized controlled trial month download article/chapter high-intensity interval training 000 mg elemental calcium/day menopausal australian-born women bone mineral density age-related differences bone turnover markers reducing bone turnover full article pdf 500 iu vitamin d3/day 800 iu vitamin d3/day related subjects high dietary calcium privacy choices/manage cookies low bone mass 25-dihydroxyvitamin d3 suppresses high-dose vitamin osteopenic postmenopausal women anderson ph reduced bone mass influence bone loss vitamin d3 dose standard-dose group 1-year clinical study food frequency questionnaire bone metabolism markers bone turnover early menopausal women long-term effects european economic area scope submit manuscript indolent systemic mastocytosis modest weight control patients receiving calcium weekâ+â800 iu/day conditions privacy policy standard-dose vitamin vitamin k2 supplementation accepting optional cookies article log population-based study haukeland university hospital author information authors bmd t-scoreââ¤ââ2 article grimnes randomized journal finder publish high dose article cite
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headline:The effect of high-dose vitamin D on bone mineral density and bone turnover markers in postmenopausal women with low bone massâa randomized controlled 1-year trial
description:Vitamin D is widely used in osteoporosis treatment, although the optimal dose is not known. This 1-year clinical study among 297 women aged 50â80 years old showed that a vitamin D3 dose of 6,500 IU/day was not better than the standard dose of 800 IU/day in improving bone mineral density (BMD) in the hip and spine. The purpose of this study was to determine whether a high dose of vitamin D3 was better than the standard dose in improving BMD and reducing bone turnover in postmenopausal women with reduced bone mass. The study was a 1-year randomized double-blind controlled trial comparing high-dose vitamin D3 with the standard dose. Postmenopausal women (nâ=â297) with a BMD T-scoreââ¤ââ2.0 in either lumbar spine (L2â4) or total hip were included and randomized to 6,500 IU vitamin D3/day (20,000 IU twice per weekâ+â800 IU/day) or 800 IU vitamin D3/day (placebo twice per weekâ+â800 IU/day). Both groups were given 1,000 mg elemental calcium/day. The primary endpoint was a change in BMD in total hip and lumbar spine (L2â4). After 1 year, serum 25-hydroxyvitamin D (25(OH)D) increased [mean (SD)] from 71 (23) to 185 (34)ânmol/l and from 71 (22) to 89 (17)ânmol/l in the high- and standard-dose vitamin D groups, respectively. BMD at all measurement sites was unchanged or slightly improved with no significant differences between the groups. Although bone turnover was reduced in both groups, the more pronounced reduction in serum levels of the bone formation marker P1NP in the standard-dose group may indicate that this treatment was more efficient. Adverse events did not differ between the groups. One year treatment with 6,500 IU vitamin D3/day was not better than 800 IU/day regarding BMD in vitamin D-replete postmenopausal women with reduced bone mass and was less efficient in reducing bone turnover.
datePublished:2011-09-10T00:00:00Z
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Bone mineral density
Bone turnover
Osteoporosis
Postmenopausal women
Randomized controlled trial
Vitamin D
Orthopedics
Endocrinology
Rheumatology
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headline:The effect of high-dose vitamin D on bone mineral density and bone turnover markers in postmenopausal women with low bone massâa randomized controlled 1-year trial
description:Vitamin D is widely used in osteoporosis treatment, although the optimal dose is not known. This 1-year clinical study among 297 women aged 50â80 years old showed that a vitamin D3 dose of 6,500 IU/day was not better than the standard dose of 800 IU/day in improving bone mineral density (BMD) in the hip and spine. The purpose of this study was to determine whether a high dose of vitamin D3 was better than the standard dose in improving BMD and reducing bone turnover in postmenopausal women with reduced bone mass. The study was a 1-year randomized double-blind controlled trial comparing high-dose vitamin D3 with the standard dose. Postmenopausal women (nâ=â297) with a BMD T-scoreââ¤ââ2.0 in either lumbar spine (L2â4) or total hip were included and randomized to 6,500 IU vitamin D3/day (20,000 IU twice per weekâ+â800 IU/day) or 800 IU vitamin D3/day (placebo twice per weekâ+â800 IU/day). Both groups were given 1,000 mg elemental calcium/day. The primary endpoint was a change in BMD in total hip and lumbar spine (L2â4). After 1 year, serum 25-hydroxyvitamin D (25(OH)D) increased [mean (SD)] from 71 (23) to 185 (34)ânmol/l and from 71 (22) to 89 (17)ânmol/l in the high- and standard-dose vitamin D groups, respectively. BMD at all measurement sites was unchanged or slightly improved with no significant differences between the groups. Although bone turnover was reduced in both groups, the more pronounced reduction in serum levels of the bone formation marker P1NP in the standard-dose group may indicate that this treatment was more efficient. Adverse events did not differ between the groups. One year treatment with 6,500 IU vitamin D3/day was not better than 800 IU/day regarding BMD in vitamin D-replete postmenopausal women with reduced bone mass and was less efficient in reducing bone turnover.
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Bone mineral density
Bone turnover
Osteoporosis
Postmenopausal women
Randomized controlled trial
Vitamin D
Orthopedics
Endocrinology
Rheumatology
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