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Bone mineral density and muscle mass in adults with developmental skeletal discrepancies

BACKGROUND: It was aimed to investigate the musculoskeletal status in individuals diagnosed with skeletal discrepancies. METHODS: This case–control study was performed on 35 patients with developmental skeletal discrepancies listed for orthognathic surgery as a case group and 33 patients who were no...

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Autores principales: Sharifi, Reza, Kordi, Sheida, Noravesh, Farhad, Aghababaei, Yasaman, Ramezani, Majid, Maghbooli, Zhila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208105/
https://www.ncbi.nlm.nih.gov/pubmed/35725431
http://dx.doi.org/10.1186/s12891-022-05538-9
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author Sharifi, Reza
Kordi, Sheida
Noravesh, Farhad
Aghababaei, Yasaman
Ramezani, Majid
Maghbooli, Zhila
author_facet Sharifi, Reza
Kordi, Sheida
Noravesh, Farhad
Aghababaei, Yasaman
Ramezani, Majid
Maghbooli, Zhila
author_sort Sharifi, Reza
collection PubMed
description BACKGROUND: It was aimed to investigate the musculoskeletal status in individuals diagnosed with skeletal discrepancies. METHODS: This case–control study was performed on 35 patients with developmental skeletal discrepancies listed for orthognathic surgery as a case group and 33 patients who were nominated for wisdom tooth removal as a control group. All participants were aged 18–40 years and the research was carried out in the period between May 2018 and May 2019. Dual X-ray absorptiometry (DEXA) was used to assess bone mass density at three bone sites: total hip, femoral neck, and the spinal lumbar vertebrae (L1-L4). The appendicular muscle mass index (ASMI) was measured based on the four limbs from the DEXA scan. RESULTS: Our data showed that 45.7% (16) of the case group were osteopenic or osteoporotic while in the control group only 21.2% (7) were osteopenic in at least one region (total hip, femoral neck, or lumbar) (p-value = 0.03). Regarding muscle mass, there was significantly lower SMI in subjects with skeletal discrepancies (case group) compared with the control group (median (IQR) 5.9 (2.5) vs. 6.8 (2.9) (kg/m2), respectively, p = 0.04). CONCLUSIONS: There is an essential need for more studies to understand the exact interrelationship between musculoskeletal status and skeletal jaw discrepancies.
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spelling pubmed-92081052022-06-21 Bone mineral density and muscle mass in adults with developmental skeletal discrepancies Sharifi, Reza Kordi, Sheida Noravesh, Farhad Aghababaei, Yasaman Ramezani, Majid Maghbooli, Zhila BMC Musculoskelet Disord Research BACKGROUND: It was aimed to investigate the musculoskeletal status in individuals diagnosed with skeletal discrepancies. METHODS: This case–control study was performed on 35 patients with developmental skeletal discrepancies listed for orthognathic surgery as a case group and 33 patients who were nominated for wisdom tooth removal as a control group. All participants were aged 18–40 years and the research was carried out in the period between May 2018 and May 2019. Dual X-ray absorptiometry (DEXA) was used to assess bone mass density at three bone sites: total hip, femoral neck, and the spinal lumbar vertebrae (L1-L4). The appendicular muscle mass index (ASMI) was measured based on the four limbs from the DEXA scan. RESULTS: Our data showed that 45.7% (16) of the case group were osteopenic or osteoporotic while in the control group only 21.2% (7) were osteopenic in at least one region (total hip, femoral neck, or lumbar) (p-value = 0.03). Regarding muscle mass, there was significantly lower SMI in subjects with skeletal discrepancies (case group) compared with the control group (median (IQR) 5.9 (2.5) vs. 6.8 (2.9) (kg/m2), respectively, p = 0.04). CONCLUSIONS: There is an essential need for more studies to understand the exact interrelationship between musculoskeletal status and skeletal jaw discrepancies. BioMed Central 2022-06-20 /pmc/articles/PMC9208105/ /pubmed/35725431 http://dx.doi.org/10.1186/s12891-022-05538-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sharifi, Reza
Kordi, Sheida
Noravesh, Farhad
Aghababaei, Yasaman
Ramezani, Majid
Maghbooli, Zhila
Bone mineral density and muscle mass in adults with developmental skeletal discrepancies
title Bone mineral density and muscle mass in adults with developmental skeletal discrepancies
title_full Bone mineral density and muscle mass in adults with developmental skeletal discrepancies
title_fullStr Bone mineral density and muscle mass in adults with developmental skeletal discrepancies
title_full_unstemmed Bone mineral density and muscle mass in adults with developmental skeletal discrepancies
title_short Bone mineral density and muscle mass in adults with developmental skeletal discrepancies
title_sort bone mineral density and muscle mass in adults with developmental skeletal discrepancies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9208105/
https://www.ncbi.nlm.nih.gov/pubmed/35725431
http://dx.doi.org/10.1186/s12891-022-05538-9
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