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The risk of dementia in multiple sclerosis and neuromyelitis optica spectrum disorder
INTRODUCTION: Cognitive impairment is a common feature of multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). However, there is a lack of population-based study of dementia risk in these disorders. In the present study, the risk of dementia in MS and NMOSD patients in Republi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309000/ https://www.ncbi.nlm.nih.gov/pubmed/37397465 http://dx.doi.org/10.3389/fnins.2023.1214652 |
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author | Cho, Eun Bin Jung, Se Young Jung, Jin-Hyung Yeo, Yohwan Kim, Hee Jin Han, Kyungdo Shin, Dong Wook Min, Ju-Hong |
author_facet | Cho, Eun Bin Jung, Se Young Jung, Jin-Hyung Yeo, Yohwan Kim, Hee Jin Han, Kyungdo Shin, Dong Wook Min, Ju-Hong |
author_sort | Cho, Eun Bin |
collection | PubMed |
description | INTRODUCTION: Cognitive impairment is a common feature of multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). However, there is a lack of population-based study of dementia risk in these disorders. In the present study, the risk of dementia in MS and NMOSD patients in Republic of Korea was estimated. METHODS: Data analyzed in this study were obtained from the Korean National Health Insurance Service (KNHIS) database between January 2010 and December 2017. The study included 1,347 MS patients and 1,460 NMOSD patients ≥40 years of age who had not been diagnosed with dementia within 1 year prior to the index date. Matched controls were selected based on age, sex, and the presence of hypertension, diabetes mellitus, or dyslipidemia. RESULTS: In MS and NMOSD patients, the risk of developing any dementia [adjusted hazard ratio (aHR) = 2.34; 95% confidence interval (CI) = 1.84–2.96 and aHR = 2.19; 95% CI = 1.61–3.00, respectively], Alzheimer’s disease [AD; aHR = 2.23; 95% confidence interval (CI) = 1.70–2.91 and aHR = 1.99; 95% CI = 1.38–2.88, respectively], and vascular dementia (aHR = 3.75; 95% CI = 1.91–7.35 and aHR = 3.21; 95% CI = 1.47–7.02, respectively) was higher compared with the matched controls. NMOSD patients had a lower risk of any dementia and AD compared with MS patients after adjusting for age, sex, income, hypertension, diabetes, and dyslipidemia (aHR = 0.67 and 0.62). CONCLUSION: The risk of dementia increased in MS and NMOSD patients and dementia risk was higher in MS than in NMOSD. |
format | Online Article Text |
id | pubmed-10309000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103090002023-06-30 The risk of dementia in multiple sclerosis and neuromyelitis optica spectrum disorder Cho, Eun Bin Jung, Se Young Jung, Jin-Hyung Yeo, Yohwan Kim, Hee Jin Han, Kyungdo Shin, Dong Wook Min, Ju-Hong Front Neurosci Neuroscience INTRODUCTION: Cognitive impairment is a common feature of multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). However, there is a lack of population-based study of dementia risk in these disorders. In the present study, the risk of dementia in MS and NMOSD patients in Republic of Korea was estimated. METHODS: Data analyzed in this study were obtained from the Korean National Health Insurance Service (KNHIS) database between January 2010 and December 2017. The study included 1,347 MS patients and 1,460 NMOSD patients ≥40 years of age who had not been diagnosed with dementia within 1 year prior to the index date. Matched controls were selected based on age, sex, and the presence of hypertension, diabetes mellitus, or dyslipidemia. RESULTS: In MS and NMOSD patients, the risk of developing any dementia [adjusted hazard ratio (aHR) = 2.34; 95% confidence interval (CI) = 1.84–2.96 and aHR = 2.19; 95% CI = 1.61–3.00, respectively], Alzheimer’s disease [AD; aHR = 2.23; 95% confidence interval (CI) = 1.70–2.91 and aHR = 1.99; 95% CI = 1.38–2.88, respectively], and vascular dementia (aHR = 3.75; 95% CI = 1.91–7.35 and aHR = 3.21; 95% CI = 1.47–7.02, respectively) was higher compared with the matched controls. NMOSD patients had a lower risk of any dementia and AD compared with MS patients after adjusting for age, sex, income, hypertension, diabetes, and dyslipidemia (aHR = 0.67 and 0.62). CONCLUSION: The risk of dementia increased in MS and NMOSD patients and dementia risk was higher in MS than in NMOSD. Frontiers Media S.A. 2023-06-15 /pmc/articles/PMC10309000/ /pubmed/37397465 http://dx.doi.org/10.3389/fnins.2023.1214652 Text en Copyright © 2023 Cho, Jung, Jung, Yeo, Kim, Han, Shin and Min. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Cho, Eun Bin Jung, Se Young Jung, Jin-Hyung Yeo, Yohwan Kim, Hee Jin Han, Kyungdo Shin, Dong Wook Min, Ju-Hong The risk of dementia in multiple sclerosis and neuromyelitis optica spectrum disorder |
title | The risk of dementia in multiple sclerosis and neuromyelitis optica spectrum disorder |
title_full | The risk of dementia in multiple sclerosis and neuromyelitis optica spectrum disorder |
title_fullStr | The risk of dementia in multiple sclerosis and neuromyelitis optica spectrum disorder |
title_full_unstemmed | The risk of dementia in multiple sclerosis and neuromyelitis optica spectrum disorder |
title_short | The risk of dementia in multiple sclerosis and neuromyelitis optica spectrum disorder |
title_sort | risk of dementia in multiple sclerosis and neuromyelitis optica spectrum disorder |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309000/ https://www.ncbi.nlm.nih.gov/pubmed/37397465 http://dx.doi.org/10.3389/fnins.2023.1214652 |
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