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The potential impact of sleep-related movement disorders on stroke risk: a population-based longitudinal study

BACKGROUND: Sleep-related movement disorders (SRMD) have been shown to increase the risk of cardiovascular diseases. However, the relationship between SRMD and stroke remains unclear. AIM: To explore the relationship between SRMD and stroke in the general population. DESIGN: Two cohorts of patients...

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Autores principales: Chou, C-H, Yin, J-H, Chen, S-Y, Lin, C-C, Sung, Y-F, Chung, C-H, Chien, W-C, Tsai, C-K, Tsai, C-L, Lin, G-Y, Lin, Y-K, Lee, J-T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5914305/
https://www.ncbi.nlm.nih.gov/pubmed/28482057
http://dx.doi.org/10.1093/qjmed/hcx097
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author Chou, C-H
Yin, J-H
Chen, S-Y
Lin, C-C
Sung, Y-F
Chung, C-H
Chien, W-C
Tsai, C-K
Tsai, C-L
Lin, G-Y
Lin, Y-K
Lee, J-T
author_facet Chou, C-H
Yin, J-H
Chen, S-Y
Lin, C-C
Sung, Y-F
Chung, C-H
Chien, W-C
Tsai, C-K
Tsai, C-L
Lin, G-Y
Lin, Y-K
Lee, J-T
author_sort Chou, C-H
collection PubMed
description BACKGROUND: Sleep-related movement disorders (SRMD) have been shown to increase the risk of cardiovascular diseases. However, the relationship between SRMD and stroke remains unclear. AIM: To explore the relationship between SRMD and stroke in the general population. DESIGN: Two cohorts of patients with SRMD and without SRMD were followed up for the occurrence of hemorrhagic and ischemic stroke. METHODS: The study cohort enrolled 604 patients who were initially diagnosed as SRMD between 2000 and 2005. 2,416 age- and sex-matched patients without prior stroke were selected as the comparison cohort. A Cox-proportional hazard regression analysis was performed for multivariate adjustment. RESULTS: Patients with SRMD had a higher risk for developing all-cause stroke [adjusted hazard ratio (HR) = 2.29, 95% confidence interval (CI) = 1.42–3.80]. Patients of below 45 years old had the greatest stroke risk (HR = 4.03, 95% CI = 3.11–5.62), followed by patients aged ≥65 years (HR = 2.64, 95% CI = 1.12–3.44) and 45–64 years (HR = 1.07, 95% CI = 1.02–1.71). The age-stratified analysis suggested that the increased risk of hemorrhagic stroke was more significant than ischemic stroke among all age groups. Furthermore, males with SRMD were at greater risk to develop all-cause stroke (HR = 2.98, 95% CI = 1.74–4.50) than that of females (HR = 1.94, 95% CI = 1.01–3.77). CONCLUSIONS: Patients with SRMD were found to have an increased risk of all-cause stroke along with a higher possibility of hemorrhagic stroke over ischemic stroke.
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spelling pubmed-59143052018-05-04 The potential impact of sleep-related movement disorders on stroke risk: a population-based longitudinal study Chou, C-H Yin, J-H Chen, S-Y Lin, C-C Sung, Y-F Chung, C-H Chien, W-C Tsai, C-K Tsai, C-L Lin, G-Y Lin, Y-K Lee, J-T QJM Original Papers BACKGROUND: Sleep-related movement disorders (SRMD) have been shown to increase the risk of cardiovascular diseases. However, the relationship between SRMD and stroke remains unclear. AIM: To explore the relationship between SRMD and stroke in the general population. DESIGN: Two cohorts of patients with SRMD and without SRMD were followed up for the occurrence of hemorrhagic and ischemic stroke. METHODS: The study cohort enrolled 604 patients who were initially diagnosed as SRMD between 2000 and 2005. 2,416 age- and sex-matched patients without prior stroke were selected as the comparison cohort. A Cox-proportional hazard regression analysis was performed for multivariate adjustment. RESULTS: Patients with SRMD had a higher risk for developing all-cause stroke [adjusted hazard ratio (HR) = 2.29, 95% confidence interval (CI) = 1.42–3.80]. Patients of below 45 years old had the greatest stroke risk (HR = 4.03, 95% CI = 3.11–5.62), followed by patients aged ≥65 years (HR = 2.64, 95% CI = 1.12–3.44) and 45–64 years (HR = 1.07, 95% CI = 1.02–1.71). The age-stratified analysis suggested that the increased risk of hemorrhagic stroke was more significant than ischemic stroke among all age groups. Furthermore, males with SRMD were at greater risk to develop all-cause stroke (HR = 2.98, 95% CI = 1.74–4.50) than that of females (HR = 1.94, 95% CI = 1.01–3.77). CONCLUSIONS: Patients with SRMD were found to have an increased risk of all-cause stroke along with a higher possibility of hemorrhagic stroke over ischemic stroke. Oxford University Press 2017-10 2017-05-08 /pmc/articles/PMC5914305/ /pubmed/28482057 http://dx.doi.org/10.1093/qjmed/hcx097 Text en © The Author 2017. Published by Oxford University Press on behalf of the Association of Physicians. 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/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Papers
Chou, C-H
Yin, J-H
Chen, S-Y
Lin, C-C
Sung, Y-F
Chung, C-H
Chien, W-C
Tsai, C-K
Tsai, C-L
Lin, G-Y
Lin, Y-K
Lee, J-T
The potential impact of sleep-related movement disorders on stroke risk: a population-based longitudinal study
title The potential impact of sleep-related movement disorders on stroke risk: a population-based longitudinal study
title_full The potential impact of sleep-related movement disorders on stroke risk: a population-based longitudinal study
title_fullStr The potential impact of sleep-related movement disorders on stroke risk: a population-based longitudinal study
title_full_unstemmed The potential impact of sleep-related movement disorders on stroke risk: a population-based longitudinal study
title_short The potential impact of sleep-related movement disorders on stroke risk: a population-based longitudinal study
title_sort potential impact of sleep-related movement disorders on stroke risk: a population-based longitudinal study
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5914305/
https://www.ncbi.nlm.nih.gov/pubmed/28482057
http://dx.doi.org/10.1093/qjmed/hcx097
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