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Clinical characteristics of geriatric patients with non-specific chronic low back pain
A comprehensive analysis of clinical information in patients with chronic low back pain (CLBP) was performed to clarify the clinical characteristics of geriatric LBP from the perspective of body composition, spinal alignment, and blood findings related to senescence. We enrolled 203 patients with an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789852/ https://www.ncbi.nlm.nih.gov/pubmed/35079089 http://dx.doi.org/10.1038/s41598-022-05352-2 |
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author | Sakai, Yoshihito Wakao, Norimitsu Matsui, Hiroki Watanabe, Tsuyoshi Iida, Hiroki Watanabe, Ken |
author_facet | Sakai, Yoshihito Wakao, Norimitsu Matsui, Hiroki Watanabe, Tsuyoshi Iida, Hiroki Watanabe, Ken |
author_sort | Sakai, Yoshihito |
collection | PubMed |
description | A comprehensive analysis of clinical information in patients with chronic low back pain (CLBP) was performed to clarify the clinical characteristics of geriatric LBP from the perspective of body composition, spinal alignment, and blood findings related to senescence. We enrolled 203 patients with an average age of 79.0 years (77 men and 126 women), with non-specific CLBP as a single-center prospective cohort study, the patients were compared with age- and sex-matched controls without CLBP using a propensity score-matching. We performed laboratory analysis, radiographic evaluations for global spinal parameter and lumbar degeneration, and body composition analysis using whole-body dual-energy X-ray absorptiometry. We observed a higher red blood cell distribution width (RDW) (p < 0.001), which is an index of aging, as well as a lower vitamin D level (p = 0.002), skeletal muscle mass index (p = 0.045) and a higher fat mass (p = 0.007) in patients with CLBP. Moreover, patients with geriatric CLBP had significantly lower lumbar lordosis (p = 0.024), and higher sagittal vertical axis (p = 0.006) was correlated with lower extremity and trunk muscle mass (p < 0.001), independent of lumbar degeneration. Geriatric patients with CLBP have sarcopenic fat accumulation and spinal sagittal malalignment with senescent status, such as elevated RDW and hypovitaminosis D. |
format | Online Article Text |
id | pubmed-8789852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87898522022-01-27 Clinical characteristics of geriatric patients with non-specific chronic low back pain Sakai, Yoshihito Wakao, Norimitsu Matsui, Hiroki Watanabe, Tsuyoshi Iida, Hiroki Watanabe, Ken Sci Rep Article A comprehensive analysis of clinical information in patients with chronic low back pain (CLBP) was performed to clarify the clinical characteristics of geriatric LBP from the perspective of body composition, spinal alignment, and blood findings related to senescence. We enrolled 203 patients with an average age of 79.0 years (77 men and 126 women), with non-specific CLBP as a single-center prospective cohort study, the patients were compared with age- and sex-matched controls without CLBP using a propensity score-matching. We performed laboratory analysis, radiographic evaluations for global spinal parameter and lumbar degeneration, and body composition analysis using whole-body dual-energy X-ray absorptiometry. We observed a higher red blood cell distribution width (RDW) (p < 0.001), which is an index of aging, as well as a lower vitamin D level (p = 0.002), skeletal muscle mass index (p = 0.045) and a higher fat mass (p = 0.007) in patients with CLBP. Moreover, patients with geriatric CLBP had significantly lower lumbar lordosis (p = 0.024), and higher sagittal vertical axis (p = 0.006) was correlated with lower extremity and trunk muscle mass (p < 0.001), independent of lumbar degeneration. Geriatric patients with CLBP have sarcopenic fat accumulation and spinal sagittal malalignment with senescent status, such as elevated RDW and hypovitaminosis D. Nature Publishing Group UK 2022-01-25 /pmc/articles/PMC8789852/ /pubmed/35079089 http://dx.doi.org/10.1038/s41598-022-05352-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article Sakai, Yoshihito Wakao, Norimitsu Matsui, Hiroki Watanabe, Tsuyoshi Iida, Hiroki Watanabe, Ken Clinical characteristics of geriatric patients with non-specific chronic low back pain |
title | Clinical characteristics of geriatric patients with non-specific chronic low back pain |
title_full | Clinical characteristics of geriatric patients with non-specific chronic low back pain |
title_fullStr | Clinical characteristics of geriatric patients with non-specific chronic low back pain |
title_full_unstemmed | Clinical characteristics of geriatric patients with non-specific chronic low back pain |
title_short | Clinical characteristics of geriatric patients with non-specific chronic low back pain |
title_sort | clinical characteristics of geriatric patients with non-specific chronic low back pain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789852/ https://www.ncbi.nlm.nih.gov/pubmed/35079089 http://dx.doi.org/10.1038/s41598-022-05352-2 |
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