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Eosinopenia is a predictive factor for the severity of acute ischemic stroke

Previous data have revealed an association between eosinopenia and mortality of acute ischemic stroke. However, the relationship of eosinopenia with infarct volume, infection rate, and poor outcome of acute ischemic stroke is still unknown. The retrospective study included 421 patients (273 males, 6...

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Autores principales: Zhao, Hui-Min, Qin, Wen-Qian, Wang, Pei-Ji, Wen, Zhong-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585555/
https://www.ncbi.nlm.nih.gov/pubmed/31169195
http://dx.doi.org/10.4103/1673-5374.258411
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author Zhao, Hui-Min
Qin, Wen-Qian
Wang, Pei-Ji
Wen, Zhong-Min
author_facet Zhao, Hui-Min
Qin, Wen-Qian
Wang, Pei-Ji
Wen, Zhong-Min
author_sort Zhao, Hui-Min
collection PubMed
description Previous data have revealed an association between eosinopenia and mortality of acute ischemic stroke. However, the relationship of eosinopenia with infarct volume, infection rate, and poor outcome of acute ischemic stroke is still unknown. The retrospective study included 421 patients (273 males, 65%; mean age, 68.0 ± 13.0 years) with first acute ischemic stroke who were hospitalized in the Second Affiliated Hospital of Soochow University, China, from January 2017 to February 2018. Laboratory data, neuroimaging results, and modified Rankin Scale scores were collected. Patients were divided into four groups according to their eosinophil percentage level (< 0.4%, 0.4–1.1%, 1.1–2.3%, ≥ 2.3%). Spearman’s correlation analysis showed that the percentage of eosinophils was negatively correlated with infarct volume (r(s) = −0.514, P < 0.001). Receiver operating characteristic analysis demonstrated that eosinopenia predicted a large infarct volume more accurately than neutrophilia; the area under curve was 0.906 and 0.876, respectively; a large infarct was considered as that with a diameter larger than 3 cm and involving more than two major arterial blood supply areas. Logistic regression analysis revealed that eosinophil percentage was an independent risk factor for acute ischemic stroke (P = 0.002). Moreover, eosinophil percentage was significantly associated with large infarct volume, high infection rate (pulmonary and urinary tract infections), and poor outcome (modified Rankin Scale score > 3) after adjusting for potential confounding factors (P-trend < 0.001). These findings suggest that eosinopenia has the potential to predict the severity of acute ischemic stroke. This study was approved by the Ethics Committee of the Second Affiliated Hospital of Soochow University, China (approval number: K10) on November 10, 2015.
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spelling pubmed-65855552019-10-01 Eosinopenia is a predictive factor for the severity of acute ischemic stroke Zhao, Hui-Min Qin, Wen-Qian Wang, Pei-Ji Wen, Zhong-Min Neural Regen Res Research Article Previous data have revealed an association between eosinopenia and mortality of acute ischemic stroke. However, the relationship of eosinopenia with infarct volume, infection rate, and poor outcome of acute ischemic stroke is still unknown. The retrospective study included 421 patients (273 males, 65%; mean age, 68.0 ± 13.0 years) with first acute ischemic stroke who were hospitalized in the Second Affiliated Hospital of Soochow University, China, from January 2017 to February 2018. Laboratory data, neuroimaging results, and modified Rankin Scale scores were collected. Patients were divided into four groups according to their eosinophil percentage level (< 0.4%, 0.4–1.1%, 1.1–2.3%, ≥ 2.3%). Spearman’s correlation analysis showed that the percentage of eosinophils was negatively correlated with infarct volume (r(s) = −0.514, P < 0.001). Receiver operating characteristic analysis demonstrated that eosinopenia predicted a large infarct volume more accurately than neutrophilia; the area under curve was 0.906 and 0.876, respectively; a large infarct was considered as that with a diameter larger than 3 cm and involving more than two major arterial blood supply areas. Logistic regression analysis revealed that eosinophil percentage was an independent risk factor for acute ischemic stroke (P = 0.002). Moreover, eosinophil percentage was significantly associated with large infarct volume, high infection rate (pulmonary and urinary tract infections), and poor outcome (modified Rankin Scale score > 3) after adjusting for potential confounding factors (P-trend < 0.001). These findings suggest that eosinopenia has the potential to predict the severity of acute ischemic stroke. This study was approved by the Ethics Committee of the Second Affiliated Hospital of Soochow University, China (approval number: K10) on November 10, 2015. Wolters Kluwer - Medknow 2019-10 /pmc/articles/PMC6585555/ /pubmed/31169195 http://dx.doi.org/10.4103/1673-5374.258411 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Zhao, Hui-Min
Qin, Wen-Qian
Wang, Pei-Ji
Wen, Zhong-Min
Eosinopenia is a predictive factor for the severity of acute ischemic stroke
title Eosinopenia is a predictive factor for the severity of acute ischemic stroke
title_full Eosinopenia is a predictive factor for the severity of acute ischemic stroke
title_fullStr Eosinopenia is a predictive factor for the severity of acute ischemic stroke
title_full_unstemmed Eosinopenia is a predictive factor for the severity of acute ischemic stroke
title_short Eosinopenia is a predictive factor for the severity of acute ischemic stroke
title_sort eosinopenia is a predictive factor for the severity of acute ischemic stroke
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585555/
https://www.ncbi.nlm.nih.gov/pubmed/31169195
http://dx.doi.org/10.4103/1673-5374.258411
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