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Association between metabolic syndrome and multiple lesions of intracranial atherothrombotic stroke: a hospital-based study

BACKGROUND: With the increasing trend of metabolic syndrome (MetS) and atherothrombotic stroke (which can manifest as stroke lesion multiplicity), studies on the association between MetS and the clinical aspects of atherothrombotic stroke are of great interest. The present study aimed to investigate...

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Autores principales: Kotani, Kazuhiko, Satoh-Asahara, Noriko, Nakakuki, Takuya, Yamakage, Hajime, Shimatsu, Akira, Tsukahara, Tetsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535534/
https://www.ncbi.nlm.nih.gov/pubmed/26269150
http://dx.doi.org/10.1186/s12933-015-0272-6
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author Kotani, Kazuhiko
Satoh-Asahara, Noriko
Nakakuki, Takuya
Yamakage, Hajime
Shimatsu, Akira
Tsukahara, Tetsuya
author_facet Kotani, Kazuhiko
Satoh-Asahara, Noriko
Nakakuki, Takuya
Yamakage, Hajime
Shimatsu, Akira
Tsukahara, Tetsuya
author_sort Kotani, Kazuhiko
collection PubMed
description BACKGROUND: With the increasing trend of metabolic syndrome (MetS) and atherothrombotic stroke (which can manifest as stroke lesion multiplicity), studies on the association between MetS and the clinical aspects of atherothrombotic stroke are of great interest. The present study aimed to investigate the association between MetS and multiple atherothrombotic strokes in patients with intracranial atherothrombotic stroke. METHODS: A retrospective study based on medical charts was conducted among patients (n = 202: 137 men/65 women) who were symptomatically admitted to the hospital with the first-ever atherothrombotic stroke. For the occurrence of multiple lesions of stroke, odds ratio [OR: 95 % confidence interval (CI)] of MetS or its respective components was calculated using logistic regression models. RESULTS: Fifty-one percent of the men and 38 % of women with stroke presented multiple regions. MetS was a significant factor that was associated with an increased risk of multiple regions in women [OR 4.3 (95 % CI 1.4–13.5)], but not in men. According to the components of MetS, dyslipidemia was a significant factor that was positively associated with multiple regions in both men [OR 2.0 (95 % CI 1.1–3.7)] and women [OR 3.2 (95 % CI 1.1–9.1)]. CONCLUSION: MetS may be pathophysiologically associated with intracranial atherothrombotic stroke multiplicity in women in particular. Future studies are warranted to confirm the findings.
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spelling pubmed-45355342015-08-14 Association between metabolic syndrome and multiple lesions of intracranial atherothrombotic stroke: a hospital-based study Kotani, Kazuhiko Satoh-Asahara, Noriko Nakakuki, Takuya Yamakage, Hajime Shimatsu, Akira Tsukahara, Tetsuya Cardiovasc Diabetol Original Investigation BACKGROUND: With the increasing trend of metabolic syndrome (MetS) and atherothrombotic stroke (which can manifest as stroke lesion multiplicity), studies on the association between MetS and the clinical aspects of atherothrombotic stroke are of great interest. The present study aimed to investigate the association between MetS and multiple atherothrombotic strokes in patients with intracranial atherothrombotic stroke. METHODS: A retrospective study based on medical charts was conducted among patients (n = 202: 137 men/65 women) who were symptomatically admitted to the hospital with the first-ever atherothrombotic stroke. For the occurrence of multiple lesions of stroke, odds ratio [OR: 95 % confidence interval (CI)] of MetS or its respective components was calculated using logistic regression models. RESULTS: Fifty-one percent of the men and 38 % of women with stroke presented multiple regions. MetS was a significant factor that was associated with an increased risk of multiple regions in women [OR 4.3 (95 % CI 1.4–13.5)], but not in men. According to the components of MetS, dyslipidemia was a significant factor that was positively associated with multiple regions in both men [OR 2.0 (95 % CI 1.1–3.7)] and women [OR 3.2 (95 % CI 1.1–9.1)]. CONCLUSION: MetS may be pathophysiologically associated with intracranial atherothrombotic stroke multiplicity in women in particular. Future studies are warranted to confirm the findings. BioMed Central 2015-08-14 /pmc/articles/PMC4535534/ /pubmed/26269150 http://dx.doi.org/10.1186/s12933-015-0272-6 Text en © Kotani et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Investigation
Kotani, Kazuhiko
Satoh-Asahara, Noriko
Nakakuki, Takuya
Yamakage, Hajime
Shimatsu, Akira
Tsukahara, Tetsuya
Association between metabolic syndrome and multiple lesions of intracranial atherothrombotic stroke: a hospital-based study
title Association between metabolic syndrome and multiple lesions of intracranial atherothrombotic stroke: a hospital-based study
title_full Association between metabolic syndrome and multiple lesions of intracranial atherothrombotic stroke: a hospital-based study
title_fullStr Association between metabolic syndrome and multiple lesions of intracranial atherothrombotic stroke: a hospital-based study
title_full_unstemmed Association between metabolic syndrome and multiple lesions of intracranial atherothrombotic stroke: a hospital-based study
title_short Association between metabolic syndrome and multiple lesions of intracranial atherothrombotic stroke: a hospital-based study
title_sort association between metabolic syndrome and multiple lesions of intracranial atherothrombotic stroke: a hospital-based study
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535534/
https://www.ncbi.nlm.nih.gov/pubmed/26269150
http://dx.doi.org/10.1186/s12933-015-0272-6
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