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Metabolic Syndrome is a Predisposing Factor for Diffuse Idiopathic Skeletal Hyperostosis
OBJECTIVE: Diffuse idiopathic skeletal hyperostosis (DISH) causes spinal ankylosis, which can result in patients suffering specific spinal fractures that lead to a reduction in the activities of daily life in older patients. Currently, DISH is associated with diabetes mellitus and cardiovascular dis...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Spinal Neurosurgery Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021843/ https://www.ncbi.nlm.nih.gov/pubmed/33211945 http://dx.doi.org/10.14245/ns.2040350.175 |
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author | Okada, Eijiro Ishihara, Shinichi Azuma, Koichiro Michikawa, Takehiro Suzuki, Satoshi Tsuji, Osahiko Nori, Satoshi Nagoshi, Narihito Yagi, Mitsuru Takayama, Michiyo Tsuji, Takashi Fujita, Nobuyuki Nakamura, Masaya Matsumoto, Morio Watanabe, Kota |
author_facet | Okada, Eijiro Ishihara, Shinichi Azuma, Koichiro Michikawa, Takehiro Suzuki, Satoshi Tsuji, Osahiko Nori, Satoshi Nagoshi, Narihito Yagi, Mitsuru Takayama, Michiyo Tsuji, Takashi Fujita, Nobuyuki Nakamura, Masaya Matsumoto, Morio Watanabe, Kota |
author_sort | Okada, Eijiro |
collection | PubMed |
description | OBJECTIVE: Diffuse idiopathic skeletal hyperostosis (DISH) causes spinal ankylosis, which can result in patients suffering specific spinal fractures that lead to a reduction in the activities of daily life in older patients. Currently, DISH is associated with diabetes mellitus and cardiovascular disease; however, the association between DISH and metabolic syndrome has not been established. The purpose of this study was to investigate a potential association between DISH and metabolic syndrome. METHODS: We retrospectively reviewed clinical data from consecutive subjects undergoing the musculoskeletal health medical checkups, and enrolled 327 subjects (174 men and 153 women; mean, 63.4 ± 13.7-years). Subjects who had spinal ankylosis at least 4 contiguous vertebral bodies were classified as the DISH group (n = 39) while the others were part of the non-DISH group (n = 288). The definition of the metabolic syndrome comes from diagnostic criteria used by the Japanese Society for Internal Medicine. Age, sex, body max index (BMI), hematological evaluation, blood pressure, presence of metabolic syndrome, the visceral fat area on abdominal computed tomography, and spinal epidural lipomatosis (SEL) on magnetic resonance imaging were evaluated. RESULTS: Compared to the non-DISH group, in the DISH group, mean age (DISH group, 74.3 years; non-DISH group, 1.9 years; p < 0.001), male prevalence were higher (DISH group, 82.1%; non-DISH group, 49.3%; p < 0.001), and BMI was greater (DISH group, 24.8; non-DISH group, 23.0; p = 0.006). the metabolic syndrome was more frequently observed in DISH group (28.9%) than in the non-DISH group (16.0%) (p = 0.045). The visceral fat area was significantly larger in the DISH group than in the non-DISH group (DISH group, 130.7 ± 58.2 cm(2); Non-DISH group, 89.0 ± 48.1 cm(2); p < 0.001). The prevalence of SEL was similar between the 2 groups (10.3% in the DISH group vs. 8.7% in the nonDISH group; p = 0.464). Poisson regression analysis revealed that the metabolic syndrome was significantly associated with DISH with odds ratio of 2.0 (95% confidence interval, 1.0–3.7; p = 0.004). CONCLUSION: Metabolic syndrome was significantly associated with DISH. Our data showed metabolic syndrome is potentially related to DISH. |
format | Online Article Text |
id | pubmed-8021843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Korean Spinal Neurosurgery Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80218432021-04-13 Metabolic Syndrome is a Predisposing Factor for Diffuse Idiopathic Skeletal Hyperostosis Okada, Eijiro Ishihara, Shinichi Azuma, Koichiro Michikawa, Takehiro Suzuki, Satoshi Tsuji, Osahiko Nori, Satoshi Nagoshi, Narihito Yagi, Mitsuru Takayama, Michiyo Tsuji, Takashi Fujita, Nobuyuki Nakamura, Masaya Matsumoto, Morio Watanabe, Kota Neurospine Original Article OBJECTIVE: Diffuse idiopathic skeletal hyperostosis (DISH) causes spinal ankylosis, which can result in patients suffering specific spinal fractures that lead to a reduction in the activities of daily life in older patients. Currently, DISH is associated with diabetes mellitus and cardiovascular disease; however, the association between DISH and metabolic syndrome has not been established. The purpose of this study was to investigate a potential association between DISH and metabolic syndrome. METHODS: We retrospectively reviewed clinical data from consecutive subjects undergoing the musculoskeletal health medical checkups, and enrolled 327 subjects (174 men and 153 women; mean, 63.4 ± 13.7-years). Subjects who had spinal ankylosis at least 4 contiguous vertebral bodies were classified as the DISH group (n = 39) while the others were part of the non-DISH group (n = 288). The definition of the metabolic syndrome comes from diagnostic criteria used by the Japanese Society for Internal Medicine. Age, sex, body max index (BMI), hematological evaluation, blood pressure, presence of metabolic syndrome, the visceral fat area on abdominal computed tomography, and spinal epidural lipomatosis (SEL) on magnetic resonance imaging were evaluated. RESULTS: Compared to the non-DISH group, in the DISH group, mean age (DISH group, 74.3 years; non-DISH group, 1.9 years; p < 0.001), male prevalence were higher (DISH group, 82.1%; non-DISH group, 49.3%; p < 0.001), and BMI was greater (DISH group, 24.8; non-DISH group, 23.0; p = 0.006). the metabolic syndrome was more frequently observed in DISH group (28.9%) than in the non-DISH group (16.0%) (p = 0.045). The visceral fat area was significantly larger in the DISH group than in the non-DISH group (DISH group, 130.7 ± 58.2 cm(2); Non-DISH group, 89.0 ± 48.1 cm(2); p < 0.001). The prevalence of SEL was similar between the 2 groups (10.3% in the DISH group vs. 8.7% in the nonDISH group; p = 0.464). Poisson regression analysis revealed that the metabolic syndrome was significantly associated with DISH with odds ratio of 2.0 (95% confidence interval, 1.0–3.7; p = 0.004). CONCLUSION: Metabolic syndrome was significantly associated with DISH. Our data showed metabolic syndrome is potentially related to DISH. Korean Spinal Neurosurgery Society 2021-03 2020-11-17 /pmc/articles/PMC8021843/ /pubmed/33211945 http://dx.doi.org/10.14245/ns.2040350.175 Text en Copyright © 2021 by the Korean Spinal Neurosurgery Society https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Okada, Eijiro Ishihara, Shinichi Azuma, Koichiro Michikawa, Takehiro Suzuki, Satoshi Tsuji, Osahiko Nori, Satoshi Nagoshi, Narihito Yagi, Mitsuru Takayama, Michiyo Tsuji, Takashi Fujita, Nobuyuki Nakamura, Masaya Matsumoto, Morio Watanabe, Kota Metabolic Syndrome is a Predisposing Factor for Diffuse Idiopathic Skeletal Hyperostosis |
title | Metabolic Syndrome is a Predisposing Factor for Diffuse Idiopathic Skeletal Hyperostosis |
title_full | Metabolic Syndrome is a Predisposing Factor for Diffuse Idiopathic Skeletal Hyperostosis |
title_fullStr | Metabolic Syndrome is a Predisposing Factor for Diffuse Idiopathic Skeletal Hyperostosis |
title_full_unstemmed | Metabolic Syndrome is a Predisposing Factor for Diffuse Idiopathic Skeletal Hyperostosis |
title_short | Metabolic Syndrome is a Predisposing Factor for Diffuse Idiopathic Skeletal Hyperostosis |
title_sort | metabolic syndrome is a predisposing factor for diffuse idiopathic skeletal hyperostosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021843/ https://www.ncbi.nlm.nih.gov/pubmed/33211945 http://dx.doi.org/10.14245/ns.2040350.175 |
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