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Is Vitamin D Deficiency associated with Non Specific Musculoskeletal Pain?
BACKGROUNDS: Vitamin D deficiency is common worldwide, including Iran. It has been suggested that vitamin D deficiency is associated with non-specific musculoskeletal pain. The aim of this study is evaluation of the association of musculoskeletal pain with vitamin D deficiency and the response of th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Canadian Center of Science and Education
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776981/ https://www.ncbi.nlm.nih.gov/pubmed/23283042 http://dx.doi.org/10.5539/gjhs.v5n1p107 |
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author | Abbasi, Mahnaz Hashemipour, Sima Hajmanuchehri, Fatemeh Kazemifar, Amir Mohammad |
author_facet | Abbasi, Mahnaz Hashemipour, Sima Hajmanuchehri, Fatemeh Kazemifar, Amir Mohammad |
author_sort | Abbasi, Mahnaz |
collection | PubMed |
description | BACKGROUNDS: Vitamin D deficiency is common worldwide, including Iran. It has been suggested that vitamin D deficiency is associated with non-specific musculoskeletal pain. The aim of this study is evaluation of the association of musculoskeletal pain with vitamin D deficiency and the response of the patients to vitamin D supplementation. MATERIALS AND METHODS: sixty two adult patients with chief complaint of musculoskeletal pain were enrolled in the study. Serum concentrations of 25(OH)D, Calcium, Phosphate, Alkaline Phosphatase and PTH were determined. If there was vitamin D deficiency, oral vitamin D supplementation was given. Assessment of pain and its response to therapy was carried out using Visual Assessment Score (VAS). SPSS software version 15.0 was used for statistical analyses. FINDINGS: Most of the patients (95.4%) had vitamin D deficiency. Pain in 53 patients (85.5%) with responded to the proposed treatment. In responder group post treatment vitamin D concentration was significantly higher than non responder group (60.6±27.6and 39.2±9.6 nmol/l respectively, p<0.01) pretreatment vitamin D and minerals concentrations and pain characteristics did not have significant differences in responder and non responder group. CONCLUSION: Treatment with vitamin D can relieve the pain in majority of the patients with vitamin D deficiency. Lack of response can be due to insufficient increase in serum vitamin D concentration. Physiologic differences of gastrointestinal vitamin D absorption, differences of body mass indexes, and noncompliance could be potential causes for this issue. Reassessment of serum 25(OH)D concentration is recommended in nonresponsive patients. |
format | Online Article Text |
id | pubmed-4776981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Canadian Center of Science and Education |
record_format | MEDLINE/PubMed |
spelling | pubmed-47769812016-04-21 Is Vitamin D Deficiency associated with Non Specific Musculoskeletal Pain? Abbasi, Mahnaz Hashemipour, Sima Hajmanuchehri, Fatemeh Kazemifar, Amir Mohammad Glob J Health Sci Articles BACKGROUNDS: Vitamin D deficiency is common worldwide, including Iran. It has been suggested that vitamin D deficiency is associated with non-specific musculoskeletal pain. The aim of this study is evaluation of the association of musculoskeletal pain with vitamin D deficiency and the response of the patients to vitamin D supplementation. MATERIALS AND METHODS: sixty two adult patients with chief complaint of musculoskeletal pain were enrolled in the study. Serum concentrations of 25(OH)D, Calcium, Phosphate, Alkaline Phosphatase and PTH were determined. If there was vitamin D deficiency, oral vitamin D supplementation was given. Assessment of pain and its response to therapy was carried out using Visual Assessment Score (VAS). SPSS software version 15.0 was used for statistical analyses. FINDINGS: Most of the patients (95.4%) had vitamin D deficiency. Pain in 53 patients (85.5%) with responded to the proposed treatment. In responder group post treatment vitamin D concentration was significantly higher than non responder group (60.6±27.6and 39.2±9.6 nmol/l respectively, p<0.01) pretreatment vitamin D and minerals concentrations and pain characteristics did not have significant differences in responder and non responder group. CONCLUSION: Treatment with vitamin D can relieve the pain in majority of the patients with vitamin D deficiency. Lack of response can be due to insufficient increase in serum vitamin D concentration. Physiologic differences of gastrointestinal vitamin D absorption, differences of body mass indexes, and noncompliance could be potential causes for this issue. Reassessment of serum 25(OH)D concentration is recommended in nonresponsive patients. Canadian Center of Science and Education 2013-01 2012-11-11 /pmc/articles/PMC4776981/ /pubmed/23283042 http://dx.doi.org/10.5539/gjhs.v5n1p107 Text en Copyright: © Canadian Center of Science and Education http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Abbasi, Mahnaz Hashemipour, Sima Hajmanuchehri, Fatemeh Kazemifar, Amir Mohammad Is Vitamin D Deficiency associated with Non Specific Musculoskeletal Pain? |
title | Is Vitamin D Deficiency associated with Non Specific Musculoskeletal Pain? |
title_full | Is Vitamin D Deficiency associated with Non Specific Musculoskeletal Pain? |
title_fullStr | Is Vitamin D Deficiency associated with Non Specific Musculoskeletal Pain? |
title_full_unstemmed | Is Vitamin D Deficiency associated with Non Specific Musculoskeletal Pain? |
title_short | Is Vitamin D Deficiency associated with Non Specific Musculoskeletal Pain? |
title_sort | is vitamin d deficiency associated with non specific musculoskeletal pain? |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776981/ https://www.ncbi.nlm.nih.gov/pubmed/23283042 http://dx.doi.org/10.5539/gjhs.v5n1p107 |
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