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Identification of vitamin D and other bone metabolism parameters as risk factors for primary bone marrow oedema syndrome

BACKGROUND: The aetiology and pathogenesis of primary bone marrow oedema syndrome (BMES) remain unclear. This retrospective cross-sectional study in a large cohort of patients with BMES was performed to characterise the overall skeletal status and turnover in patients with BMES, with the aim of iden...

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Autores principales: Oehler, Nicola, Mussawy, Haider, Schmidt, Tobias, Rolvien, Tim, Barvencik, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303903/
https://www.ncbi.nlm.nih.gov/pubmed/30579337
http://dx.doi.org/10.1186/s12891-018-2379-x
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author Oehler, Nicola
Mussawy, Haider
Schmidt, Tobias
Rolvien, Tim
Barvencik, Florian
author_facet Oehler, Nicola
Mussawy, Haider
Schmidt, Tobias
Rolvien, Tim
Barvencik, Florian
author_sort Oehler, Nicola
collection PubMed
description BACKGROUND: The aetiology and pathogenesis of primary bone marrow oedema syndrome (BMES) remain unclear. This retrospective cross-sectional study in a large cohort of patients with BMES was performed to characterise the overall skeletal status and turnover in patients with BMES, with the aim of identifying risk factors for this disease. METHODS: Patients who were diagnosed with BMES on the basis of clinical and radiological (magnetic resonance imaging) findings in our outpatient clinic were identified retrospectively. Patient history, co-existing metabolic disorders, bone metabolism parameters (serum calcium, phosphate, 25-OH-D(3), bone-specific alkaline phosphatase, parathyroid hormone, and osteocalcin, and urinary deoxypyridinoline) and bone mineral density (as measured by dual-energy X-ray absorptiometry) were extracted from the medical records. Patients with secondary causes for BMES were excluded from the study. RESULTS: Of the 171 patients, 65 were identified without secondary cause for BMES. Of the 65 patients, 61.5% were female. The mean age was 49.5 ± 16.7 years, and age-related BMES prevalence showed two peaks, one in adolescence (11–20 years) and one at an older age (51–70 years). BMES predominantly affected the weight-bearing joints, namely, the ankle/foot (55.1%), knee (22.4%) and proximal femur (16.3%). Thyroid disorders and secondary hyperparathyroidism were highly prevalent (21.5 and 21.4%, respectively). On average, the cohort had elevated deoxypyridinoline levels and low 25-OH-D(3) levels (19.0 ± 7.5 μg/l in patients without vitamin D supplementation). Osteopenia and osteoporosis were diagnosed in 47.4 and 17.5% of patients, respectively. CONCLUSIONS: BMES is associated with high bone turnover. Patients who are diagnosed with BMES should be screened carefully for bone metabolism disorders and their potential risk factors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12891-018-2379-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-63039032018-12-31 Identification of vitamin D and other bone metabolism parameters as risk factors for primary bone marrow oedema syndrome Oehler, Nicola Mussawy, Haider Schmidt, Tobias Rolvien, Tim Barvencik, Florian BMC Musculoskelet Disord Research Article BACKGROUND: The aetiology and pathogenesis of primary bone marrow oedema syndrome (BMES) remain unclear. This retrospective cross-sectional study in a large cohort of patients with BMES was performed to characterise the overall skeletal status and turnover in patients with BMES, with the aim of identifying risk factors for this disease. METHODS: Patients who were diagnosed with BMES on the basis of clinical and radiological (magnetic resonance imaging) findings in our outpatient clinic were identified retrospectively. Patient history, co-existing metabolic disorders, bone metabolism parameters (serum calcium, phosphate, 25-OH-D(3), bone-specific alkaline phosphatase, parathyroid hormone, and osteocalcin, and urinary deoxypyridinoline) and bone mineral density (as measured by dual-energy X-ray absorptiometry) were extracted from the medical records. Patients with secondary causes for BMES were excluded from the study. RESULTS: Of the 171 patients, 65 were identified without secondary cause for BMES. Of the 65 patients, 61.5% were female. The mean age was 49.5 ± 16.7 years, and age-related BMES prevalence showed two peaks, one in adolescence (11–20 years) and one at an older age (51–70 years). BMES predominantly affected the weight-bearing joints, namely, the ankle/foot (55.1%), knee (22.4%) and proximal femur (16.3%). Thyroid disorders and secondary hyperparathyroidism were highly prevalent (21.5 and 21.4%, respectively). On average, the cohort had elevated deoxypyridinoline levels and low 25-OH-D(3) levels (19.0 ± 7.5 μg/l in patients without vitamin D supplementation). Osteopenia and osteoporosis were diagnosed in 47.4 and 17.5% of patients, respectively. CONCLUSIONS: BMES is associated with high bone turnover. Patients who are diagnosed with BMES should be screened carefully for bone metabolism disorders and their potential risk factors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12891-018-2379-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-22 /pmc/articles/PMC6303903/ /pubmed/30579337 http://dx.doi.org/10.1186/s12891-018-2379-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Oehler, Nicola
Mussawy, Haider
Schmidt, Tobias
Rolvien, Tim
Barvencik, Florian
Identification of vitamin D and other bone metabolism parameters as risk factors for primary bone marrow oedema syndrome
title Identification of vitamin D and other bone metabolism parameters as risk factors for primary bone marrow oedema syndrome
title_full Identification of vitamin D and other bone metabolism parameters as risk factors for primary bone marrow oedema syndrome
title_fullStr Identification of vitamin D and other bone metabolism parameters as risk factors for primary bone marrow oedema syndrome
title_full_unstemmed Identification of vitamin D and other bone metabolism parameters as risk factors for primary bone marrow oedema syndrome
title_short Identification of vitamin D and other bone metabolism parameters as risk factors for primary bone marrow oedema syndrome
title_sort identification of vitamin d and other bone metabolism parameters as risk factors for primary bone marrow oedema syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303903/
https://www.ncbi.nlm.nih.gov/pubmed/30579337
http://dx.doi.org/10.1186/s12891-018-2379-x
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