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Characteristics of cryptogenic stroke in cancer patients

OBJECTIVE: To clarify the characteristics of cryptogenic stroke in patients with active cancer. METHODS: Patients with or without cancer diagnosed with acute ischemic stroke between January 2006 and February 2015 were extracted from a prospectively collected stroke database of Osaka University Hospi...

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Autores principales: Gon, Yasufumi, Okazaki, Shuhei, Terasaki, Yasukazu, Sasaki, Tsutomu, Yoshimine, Toshiki, Sakaguchi, Manabu, Mochizuki, Hideki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818743/
https://www.ncbi.nlm.nih.gov/pubmed/27081658
http://dx.doi.org/10.1002/acn3.291
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author Gon, Yasufumi
Okazaki, Shuhei
Terasaki, Yasukazu
Sasaki, Tsutomu
Yoshimine, Toshiki
Sakaguchi, Manabu
Mochizuki, Hideki
author_facet Gon, Yasufumi
Okazaki, Shuhei
Terasaki, Yasukazu
Sasaki, Tsutomu
Yoshimine, Toshiki
Sakaguchi, Manabu
Mochizuki, Hideki
author_sort Gon, Yasufumi
collection PubMed
description OBJECTIVE: To clarify the characteristics of cryptogenic stroke in patients with active cancer. METHODS: Patients with or without cancer diagnosed with acute ischemic stroke between January 2006 and February 2015 were extracted from a prospectively collected stroke database of Osaka University Hospital. Patients were categorized according to the presence of active cancer and known stroke mechanisms. RESULTS: Among 1191 patients with acute ischemic stroke, 145 (12%) had active cancer. Patients with active cancer were diagnosed more often with cryptogenic stroke than were patients without cancer (47% vs. 12%, P < 0.001). Compared with cryptogenic stroke patients without cancer, cryptogenic stroke patients with active cancer had fewer atherosclerotic risk factors, lower nutrition status, higher plasma D‐dimer levels, and multiple vascular lesions. In a multivariate logistic analysis, plasma D‐dimer level (odds ratio [OR] per 1 standard deviation increase: 6.30; 95% confidence interval [CI]: 2.94–15.69; P < 0.001), and the presence of multiple vascular lesions (OR: 6.40; 95% CI: 2.35–18.35; P < 0.001) were independent predictors of active cancer. When comparing active cancer patients who had known stroke mechanisms with those who had cryptogenic stroke, high plasma D‐dimer levels, multiple vascular lesions, and receiving chemotherapy and/or radiation therapy were associated with cryptogenic stroke etiology. INTERPRETATION: In cryptogenic stroke, patients with active cancer has a unique pathology characterized by high plasma D‐dimer levels and multiple vascular lesions. The hypercoagulable state and malnutrition due to cancer and its treatments potentially influence the development of cryptogenic stroke in cancer patients.
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spelling pubmed-48187432016-04-14 Characteristics of cryptogenic stroke in cancer patients Gon, Yasufumi Okazaki, Shuhei Terasaki, Yasukazu Sasaki, Tsutomu Yoshimine, Toshiki Sakaguchi, Manabu Mochizuki, Hideki Ann Clin Transl Neurol Research Paper OBJECTIVE: To clarify the characteristics of cryptogenic stroke in patients with active cancer. METHODS: Patients with or without cancer diagnosed with acute ischemic stroke between January 2006 and February 2015 were extracted from a prospectively collected stroke database of Osaka University Hospital. Patients were categorized according to the presence of active cancer and known stroke mechanisms. RESULTS: Among 1191 patients with acute ischemic stroke, 145 (12%) had active cancer. Patients with active cancer were diagnosed more often with cryptogenic stroke than were patients without cancer (47% vs. 12%, P < 0.001). Compared with cryptogenic stroke patients without cancer, cryptogenic stroke patients with active cancer had fewer atherosclerotic risk factors, lower nutrition status, higher plasma D‐dimer levels, and multiple vascular lesions. In a multivariate logistic analysis, plasma D‐dimer level (odds ratio [OR] per 1 standard deviation increase: 6.30; 95% confidence interval [CI]: 2.94–15.69; P < 0.001), and the presence of multiple vascular lesions (OR: 6.40; 95% CI: 2.35–18.35; P < 0.001) were independent predictors of active cancer. When comparing active cancer patients who had known stroke mechanisms with those who had cryptogenic stroke, high plasma D‐dimer levels, multiple vascular lesions, and receiving chemotherapy and/or radiation therapy were associated with cryptogenic stroke etiology. INTERPRETATION: In cryptogenic stroke, patients with active cancer has a unique pathology characterized by high plasma D‐dimer levels and multiple vascular lesions. The hypercoagulable state and malnutrition due to cancer and its treatments potentially influence the development of cryptogenic stroke in cancer patients. John Wiley and Sons Inc. 2016-02-11 /pmc/articles/PMC4818743/ /pubmed/27081658 http://dx.doi.org/10.1002/acn3.291 Text en © 2016 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Paper
Gon, Yasufumi
Okazaki, Shuhei
Terasaki, Yasukazu
Sasaki, Tsutomu
Yoshimine, Toshiki
Sakaguchi, Manabu
Mochizuki, Hideki
Characteristics of cryptogenic stroke in cancer patients
title Characteristics of cryptogenic stroke in cancer patients
title_full Characteristics of cryptogenic stroke in cancer patients
title_fullStr Characteristics of cryptogenic stroke in cancer patients
title_full_unstemmed Characteristics of cryptogenic stroke in cancer patients
title_short Characteristics of cryptogenic stroke in cancer patients
title_sort characteristics of cryptogenic stroke in cancer patients
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818743/
https://www.ncbi.nlm.nih.gov/pubmed/27081658
http://dx.doi.org/10.1002/acn3.291
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