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We are analyzing https://link.springer.com/article/10.1007/s002230010085.

Title:
Hypovitaminosis D Myopathy Without Biochemical Signs of Osteomalacic Bone Involvement | Calcified Tissue International
Description:
The aims of this study were to investigate myopathy in relation to vitamin D status, and to study the muscular effects of vitamin D treatment on vitamin D-deficient individuals. Further, hypovitaminosis D myopathy was investigated in relation to alkaline phosphatase (ALP), the most commonly used marker for hypovitaminosis D osteopathy. Eight patients with osteomalacia had an isokinetic dynamometer test of all major muscle groups before and after 3 months of vitamin D treatment. The most pronounced improvements in muscle power were seen in the weight-bearing antigravity muscles of the lower limbs. A cross-sectional study was performed among 55 vitamin D-deficient veiled Arab women living in Denmark and 22 Danish controls. An isometric dynamometer model was used for determination of quadriceps muscle power. Both maximal voluntary contraction (MVC) and electrically stimulated values (single twitch, maximal production rate (MPR), and maximal relaxation rate (MRR)) were determined. The women underwent high-dose vitamin D treatment and were retested after 3 and 6 months. Prior to vitamin D treatment all parameters of muscle function in the group of vitamin D-deficient Arab women were significantly reduced compared with Danish controls. MVC: 259.4 Β± 11.0 N (Newton) versus 392.6 Β± 11.4 N (P < 10βˆ’6), single twitch: 47.0 Β± 1.8 N versus 74.6 Β± 2.2 N (P < 10βˆ’5), MPR 8.9 Β± 0.3 N/10 ms versus 14.3 Β± 0.4 N/10 ms (P < 10βˆ’6), MRR 4.5 Β± 0.2 N/10 ms versus 6.2 Β± 0.2 N/10 ms (P < 10βˆ’6). Muscle function was affected to a similar degree in women with and without bone involvement (as indicated by elevated ALP). After 3 months of vitamin D treatment all muscle-related parameters improved significantly. After 6 months only MVC was reduced compared with Danish controls (320.7 Β± 14.3 N (P < 0.02)), whereas all other measurements were normalized. Hypovitaminosis D myopathy is a prominent symptom of vitamin D deficiency, and severely impaired muscle function may be present even before biochemical signs of bone disease develop. Full normalization of hypovitaminosis D myopathy demands high-dose vitamin D treatment for 6 months or more. Our findings indicate that serum levels of ALP cannot be used in the screening for hypovitaminosis D myopathy. Assessment of s-25OHD is the only reliable test.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Health & Fitness
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Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

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


Based on our best estimate, this website will receive around 7,642,828 visitors per month in the current month.

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Keywords {πŸ”}

vitamin, article, myopathy, hypovitaminosis, muscle, denmark, treatment, aarhus, privacy, cookies, function, content, bone, months, women, information, publish, search, study, versus, access, data, log, journal, research, tissue, biochemical, signs, osteomalacic, involvement, glerup, mikkelsen, poulsen, ddeficient, alp, patients, danish, controls, maximal, mvc, deficiency, disease, discover, springer, optional, personal, parties, policy, find, track,

Topics {βœ’οΈ}

bone disease develop vitamin d-deficient individuals month download article/chapter weight-bearing antigravity muscles osteomalacic bone involvement related subjects privacy choices/manage cookies full article pdf metabolism cross-sectional study bone involvement major muscle groups european economic area scope submit manuscript isometric dynamometer model maximal voluntary contraction electrically stimulated values maximal production rate maximal relaxation rate significantly reduced compared receptor gene polymorphism conditions privacy policy quadriceps muscle power isokinetic dynamometer test accepting optional cookies journal finder publish article log single twitch information alkaline phosphatase article cite article glerup privacy policy personal data muscle power books a muscle function optional cookies manage preferences women reduced compared check access instant access subscription content similar content osteomalacic myopathy data protection essential cookies cookies skip full normalization

Schema {πŸ—ΊοΈ}

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         headline:Hypovitaminosis D Myopathy Without Biochemical Signs of Osteomalacic Bone Involvement
         description: The aims of this study were to investigate myopathy in relation to vitamin D status, and to study the muscular effects of vitamin D treatment on vitamin D-deficient individuals. Further, hypovitaminosis D myopathy was investigated in relation to alkaline phosphatase (ALP), the most commonly used marker for hypovitaminosis D osteopathy. Eight patients with osteomalacia had an isokinetic dynamometer test of all major muscle groups before and after 3 months of vitamin D treatment. The most pronounced improvements in muscle power were seen in the weight-bearing antigravity muscles of the lower limbs. A cross-sectional study was performed among 55 vitamin D-deficient veiled Arab women living in Denmark and 22 Danish controls. An isometric dynamometer model was used for determination of quadriceps muscle power. Both maximal voluntary contraction (MVC) and electrically stimulated values (single twitch, maximal production rate (MPR), and maximal relaxation rate (MRR)) were determined. The women underwent high-dose vitamin D treatment and were retested after 3 and 6 months. Prior to vitamin D treatment all parameters of muscle function in the group of vitamin D-deficient Arab women were significantly reduced compared with Danish controls. MVC: 259.4 Β± 11.0 N (Newton) versus 392.6 Β± 11.4 N (P < 10βˆ’6), single twitch: 47.0 Β± 1.8 N versus 74.6 Β± 2.2 N (P < 10βˆ’5), MPR 8.9 Β± 0.3 N/10 ms versus 14.3 Β± 0.4 N/10 ms (P < 10βˆ’6), MRR 4.5 Β± 0.2 N/10 ms versus 6.2 Β± 0.2 N/10 ms (P < 10βˆ’6). Muscle function was affected to a similar degree in women with and without bone involvement (as indicated by elevated ALP). After 3 months of vitamin D treatment all muscle-related parameters improved significantly. After 6 months only MVC was reduced compared with Danish controls (320.7 Β± 14.3 N (P < 0.02)), whereas all other measurements were normalized. Hypovitaminosis D myopathy is a prominent symptom of vitamin D deficiency, and severely impaired muscle function may be present even before biochemical signs of bone disease develop. Full normalization of hypovitaminosis D myopathy demands high-dose vitamin D treatment for 6 months or more. Our findings indicate that serum levels of ALP cannot be used in the screening for hypovitaminosis D myopathy. Assessment of s-25OHD is the only reliable test.
         datePublished:2014-03-22T00:00:00Z
         dateModified:2014-03-22T00:00:00Z
         pageStart:419
         pageEnd:424
         sameAs:https://doi.org/10.1007/s002230010085
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            Key words: Myopathy β€” Vitamin D β€” Osteomalaci β€” Alkaline phosphatase β€” Hypovitaminosis D myopathy.
            Biochemistry
            general
            Endocrinology
            Orthopedics
            Cell Biology
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      headline:Hypovitaminosis D Myopathy Without Biochemical Signs of Osteomalacic Bone Involvement
      description: The aims of this study were to investigate myopathy in relation to vitamin D status, and to study the muscular effects of vitamin D treatment on vitamin D-deficient individuals. Further, hypovitaminosis D myopathy was investigated in relation to alkaline phosphatase (ALP), the most commonly used marker for hypovitaminosis D osteopathy. Eight patients with osteomalacia had an isokinetic dynamometer test of all major muscle groups before and after 3 months of vitamin D treatment. The most pronounced improvements in muscle power were seen in the weight-bearing antigravity muscles of the lower limbs. A cross-sectional study was performed among 55 vitamin D-deficient veiled Arab women living in Denmark and 22 Danish controls. An isometric dynamometer model was used for determination of quadriceps muscle power. Both maximal voluntary contraction (MVC) and electrically stimulated values (single twitch, maximal production rate (MPR), and maximal relaxation rate (MRR)) were determined. The women underwent high-dose vitamin D treatment and were retested after 3 and 6 months. Prior to vitamin D treatment all parameters of muscle function in the group of vitamin D-deficient Arab women were significantly reduced compared with Danish controls. MVC: 259.4 Β± 11.0 N (Newton) versus 392.6 Β± 11.4 N (P < 10βˆ’6), single twitch: 47.0 Β± 1.8 N versus 74.6 Β± 2.2 N (P < 10βˆ’5), MPR 8.9 Β± 0.3 N/10 ms versus 14.3 Β± 0.4 N/10 ms (P < 10βˆ’6), MRR 4.5 Β± 0.2 N/10 ms versus 6.2 Β± 0.2 N/10 ms (P < 10βˆ’6). Muscle function was affected to a similar degree in women with and without bone involvement (as indicated by elevated ALP). After 3 months of vitamin D treatment all muscle-related parameters improved significantly. After 6 months only MVC was reduced compared with Danish controls (320.7 Β± 14.3 N (P < 0.02)), whereas all other measurements were normalized. Hypovitaminosis D myopathy is a prominent symptom of vitamin D deficiency, and severely impaired muscle function may be present even before biochemical signs of bone disease develop. Full normalization of hypovitaminosis D myopathy demands high-dose vitamin D treatment for 6 months or more. Our findings indicate that serum levels of ALP cannot be used in the screening for hypovitaminosis D myopathy. Assessment of s-25OHD is the only reliable test.
      datePublished:2014-03-22T00:00:00Z
      dateModified:2014-03-22T00:00:00Z
      pageStart:419
      pageEnd:424
      sameAs:https://doi.org/10.1007/s002230010085
      keywords:
         Key words: Myopathy β€” Vitamin D β€” Osteomalaci β€” Alkaline phosphatase β€” Hypovitaminosis D myopathy.
         Biochemistry
         general
         Endocrinology
         Orthopedics
         Cell Biology
      image:
      isPartOf:
         name:Calcified Tissue International
         issn:
            1432-0827
            0171-967X
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            Periodical
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      publisher:
         name:Springer-Verlag
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            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
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            name:H. Glerup
            affiliation:
                  name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark
                  address:
                     name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark, Denmark
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            name:K. Mikkelsen
            affiliation:
                  name:Primary Health Care Centre, City Vest, Aarhus, Denmark
                  address:
                     name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
                     type:PostalAddress
                  type:Organization
            type:Person
            name:L. Poulsen
            affiliation:
                  name:Primary Health Care Centre, City Vest, Aarhus, Denmark
                  address:
                     name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
                     type:PostalAddress
                  type:Organization
            type:Person
            name:E. Hass
            affiliation:
                  name:Primary Health Care Centre, City Vest, Aarhus, Denmark
                  address:
                     name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
                     type:PostalAddress
                  type:Organization
            type:Person
            name:S. Overbeck
            affiliation:
                  name:Primary Health Care Centre, City Vest, Aarhus, Denmark
                  address:
                     name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
                     type:PostalAddress
                  type:Organization
            type:Person
            name:H. Andersen
            affiliation:
                  name:Department of Neurology, Aarhus Kommunehospital, University Hospital of Aarhus, Denmark
                  address:
                     name:Department of Neurology, Aarhus Kommunehospital, University Hospital of Aarhus, Denmark, Denmark
                     type:PostalAddress
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            name:P. Charles
            affiliation:
                  name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark
                  address:
                     name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark, Denmark
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      address:
         name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
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      name:Department of Neurology, Aarhus Kommunehospital, University Hospital of Aarhus, Denmark
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         name:Department of Neurology, Aarhus Kommunehospital, University Hospital of Aarhus, Denmark, Denmark
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               name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark, Denmark
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      name:K. Mikkelsen
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            name:Primary Health Care Centre, City Vest, Aarhus, Denmark
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               name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
               type:PostalAddress
            type:Organization
      name:L. Poulsen
      affiliation:
            name:Primary Health Care Centre, City Vest, Aarhus, Denmark
            address:
               name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
               type:PostalAddress
            type:Organization
      name:E. Hass
      affiliation:
            name:Primary Health Care Centre, City Vest, Aarhus, Denmark
            address:
               name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
               type:PostalAddress
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            name:Primary Health Care Centre, City Vest, Aarhus, Denmark
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               name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
               type:PostalAddress
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            name:Department of Neurology, Aarhus Kommunehospital, University Hospital of Aarhus, Denmark
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               name:Department of Neurology, Aarhus Kommunehospital, University Hospital of Aarhus, Denmark, Denmark
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      name:P. Charles
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            name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark
            address:
               name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark, Denmark
               type:PostalAddress
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               name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark, Denmark
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      name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark, Denmark
      name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
      name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
      name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
      name:Primary Health Care Centre, City Vest, Aarhus, Denmark, Denmark
      name:Department of Neurology, Aarhus Kommunehospital, University Hospital of Aarhus, Denmark, Denmark
      name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark, Denmark
      name:Department of Endocrinology and Metabolism C, Aarhus Amtssygehus, University Hospital of Aarhus, Tage Hansensgade 2, DK-8000 Aarhus C, Denmark, Denmark
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