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We are analyzing https://link.springer.com/article/10.1007/s00198-011-1752-5.

Title:
The effect of high-dose vitamin D on bone mineral density and bone turnover markers in postmenopausal women with low bone mass—a 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 50–80 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 (n = 297) with a BMD T-score ≤ −2.0 in either lumbar spine (L2–4) or total hip were included and randomized to 6,500 IU vitamin D3/day (20,000 IU twice per week + 800 IU/day) or 800 IU vitamin D3/day (placebo twice per week + 800 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 (L2–4). After 1 year, serum 25-hydroxyvitamin D (25(OH)D) increased [mean (SD)] from 71 (23) to 185 (34) nmol/l and from 71 (22) to 89 (17) nmol/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.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {🔍}

article, bone, vitamin, google, scholar, pubmed, cas, women, norway, study, osteoporosis, postmenopausal, trial, university, randomized, year, mineral, density, turnover, controlled, grimnes, dose, serum, hospital, tromsø, research, figenschau, bmd, hydroxyvitamin, clin, privacy, cookies, content, jorde, iuday, groups, access, metabolism, supplementation, calcium, med, int, nutr, hormone, laboratory, department, data, publish, search, highdose,

Topics {✒️}

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 week + 800 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-score ≤ −2 article grimnes randomized journal finder publish high dose article cite

Schema {🗺️}

WebPage:
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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 mass—a 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 50–80 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 (n = 297) with a BMD T-score ≤ −2.0 in either lumbar spine (L2–4) or total hip were included and randomized to 6,500 IU vitamin D3/day (20,000 IU twice per week + 800 IU/day) or 800 IU vitamin D3/day (placebo twice per week + 800 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 (L2–4). After 1 year, serum 25-hydroxyvitamin D (25(OH)D) increased [mean (SD)] from 71 (23) to 185 (34) nmol/l and from 71 (22) to 89 (17) nmol/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
         dateModified:2011-09-10T00:00:00Z
         pageStart:201
         pageEnd:211
         sameAs:https://doi.org/10.1007/s00198-011-1752-5
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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 mass—a 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 50–80 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 (n = 297) with a BMD T-score ≤ −2.0 in either lumbar spine (L2–4) or total hip were included and randomized to 6,500 IU vitamin D3/day (20,000 IU twice per week + 800 IU/day) or 800 IU vitamin D3/day (placebo twice per week + 800 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 (L2–4). After 1 year, serum 25-hydroxyvitamin D (25(OH)D) increased [mean (SD)] from 71 (23) to 185 (34) nmol/l and from 71 (22) to 89 (17) nmol/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
      dateModified:2011-09-10T00:00:00Z
      pageStart:201
      pageEnd:211
      sameAs:https://doi.org/10.1007/s00198-011-1752-5
      keywords:
         Bone mineral density
         Bone turnover
         Osteoporosis
         Postmenopausal women
         Randomized controlled trial
         Vitamin D
         Orthopedics
         Endocrinology
         Rheumatology
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            name:G. Grimnes
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      address:
         name:Department of Medical Biochemistry, University Hospital of North Norway, Tromsø, Norway
         type:PostalAddress
      name:Oslo University Hospital
      address:
         name:Hormone Laboratory, Department of Endocrinology, Oslo University Hospital, Oslo, Norway
         type:PostalAddress
      name:Haukeland University Hospital
      address:
         name:Hormone Laboratory, Haukeland University Hospital, Bergen, Norway
         type:PostalAddress
      name:University of Tromsø
      address:
         name:Tromsø Endocrine Research Group, Department of Clinical Medicine, University of Tromsø, Tromsø, Norway
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      name:G. Grimnes
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            name:University of Tromsø
            address:
               name:Tromsø Endocrine Research Group, Department of Clinical Medicine, University of Tromsø, Tromsø, Norway
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            name:University of Tromsø
            address:
               name:Department of Medical Biology, University of Tromsø, Tromsø, Norway
               type:PostalAddress
            type:Organization
            name:University Hospital of North Norway
            address:
               name:Department of Medical Biochemistry, University Hospital of North Norway, Tromsø, Norway
               type:PostalAddress
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      name:P. A. Torjesen
      affiliation:
            name:Oslo University Hospital
            address:
               name:Hormone Laboratory, Department of Endocrinology, Oslo University Hospital, Oslo, Norway
               type:PostalAddress
            type:Organization
      name:B. AlmĂĽs
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            address:
               name:Hormone Laboratory, Haukeland University Hospital, Bergen, Norway
               type:PostalAddress
            type:Organization
      name:R. Jorde
      affiliation:
            name:University of Tromsø
            address:
               name:Tromsø Endocrine Research Group, Department of Clinical Medicine, University of Tromsø, Tromsø, Norway
               type:PostalAddress
            type:Organization
            name:University Hospital of North Norway
            address:
               name:Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Tromsø Endocrine Research Group, Department of Clinical Medicine, University of Tromsø, Tromsø, Norway
      name:Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway
      name:Tromsø Endocrine Research Group, Department of Clinical Medicine, University of Tromsø, Tromsø, Norway
      name:Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway
      name:Department of Medical Biology, University of Tromsø, Tromsø, Norway
      name:Department of Medical Biochemistry, University Hospital of North Norway, Tromsø, Norway
      name:Hormone Laboratory, Department of Endocrinology, Oslo University Hospital, Oslo, Norway
      name:Hormone Laboratory, Haukeland University Hospital, Bergen, Norway
      name:Tromsø Endocrine Research Group, Department of Clinical Medicine, University of Tromsø, Tromsø, Norway
      name:Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway
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