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Visinin-like protein-1 level is associated with short-term functional outcome of acute ischemic stroke: A prospective cohort study

Stroke is a serious disease that can lead to disability and death in adults, and the prediction of functional outcome is important in the management of acute ischemic stroke (AIS). Blood biomarker is a promising technique, for the measurement is fast, cheap and convenient. Visinin-like protein-1 (VI...

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Autores principales: Liu, Dengjun, Dong, Xiaoli, Yang, Rui, Guo, Hao, Wang, Tao, Xu, Guodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478586/
https://www.ncbi.nlm.nih.gov/pubmed/32118731
http://dx.doi.org/10.1097/MD.0000000000019252
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author Liu, Dengjun
Dong, Xiaoli
Yang, Rui
Guo, Hao
Wang, Tao
Xu, Guodong
author_facet Liu, Dengjun
Dong, Xiaoli
Yang, Rui
Guo, Hao
Wang, Tao
Xu, Guodong
author_sort Liu, Dengjun
collection PubMed
description Stroke is a serious disease that can lead to disability and death in adults, and the prediction of functional outcome is important in the management of acute ischemic stroke (AIS). Blood biomarker is a promising technique, for the measurement is fast, cheap and convenient. Visinin-like protein-1 (VILIP-1) is a classic stroke biomarker, thus we tried to investigate the predictive value of VILIP-1 for early functional outcomes of AIS. A total of 70 AIS patients were enrolled in our study. Venous blood samples of all patients were taken at day 3 after admission to the stroke unit, and levels of serum VILIP-1 were analyzed by the use of the enzyme-linked immunosorbent assay. All subjects underwent diffusion weighted imaging (DWI) of the brain MRI scanning at 72 hours after stroke onset, and infarct volumes were calculated. Initial neurological status was evaluated by the National Institutes of Health Stroke Scale (NIHSS) on admission. The short-term functional outcome was graded by the modified Rankin Scale (mRS) at discharge from the hospital. Baseline data between the favorable outcome group and poor outcome group were compared, and univariate and multivariable logistic regression analysis were used to identify risk factors of early functional outcome of AIS. The multivariate logistic regression analysis showed age, initial NIHSS scores and levels of VILIP had a strong association with poor clinical outcomes. Levels of serum VILIP-1 are associated with short-term functional outcomes in patients with AIS.
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spelling pubmed-74785862020-09-24 Visinin-like protein-1 level is associated with short-term functional outcome of acute ischemic stroke: A prospective cohort study Liu, Dengjun Dong, Xiaoli Yang, Rui Guo, Hao Wang, Tao Xu, Guodong Medicine (Baltimore) 5300 Stroke is a serious disease that can lead to disability and death in adults, and the prediction of functional outcome is important in the management of acute ischemic stroke (AIS). Blood biomarker is a promising technique, for the measurement is fast, cheap and convenient. Visinin-like protein-1 (VILIP-1) is a classic stroke biomarker, thus we tried to investigate the predictive value of VILIP-1 for early functional outcomes of AIS. A total of 70 AIS patients were enrolled in our study. Venous blood samples of all patients were taken at day 3 after admission to the stroke unit, and levels of serum VILIP-1 were analyzed by the use of the enzyme-linked immunosorbent assay. All subjects underwent diffusion weighted imaging (DWI) of the brain MRI scanning at 72 hours after stroke onset, and infarct volumes were calculated. Initial neurological status was evaluated by the National Institutes of Health Stroke Scale (NIHSS) on admission. The short-term functional outcome was graded by the modified Rankin Scale (mRS) at discharge from the hospital. Baseline data between the favorable outcome group and poor outcome group were compared, and univariate and multivariable logistic regression analysis were used to identify risk factors of early functional outcome of AIS. The multivariate logistic regression analysis showed age, initial NIHSS scores and levels of VILIP had a strong association with poor clinical outcomes. Levels of serum VILIP-1 are associated with short-term functional outcomes in patients with AIS. Wolters Kluwer Health 2020-02-28 /pmc/articles/PMC7478586/ /pubmed/32118731 http://dx.doi.org/10.1097/MD.0000000000019252 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 5300
Liu, Dengjun
Dong, Xiaoli
Yang, Rui
Guo, Hao
Wang, Tao
Xu, Guodong
Visinin-like protein-1 level is associated with short-term functional outcome of acute ischemic stroke: A prospective cohort study
title Visinin-like protein-1 level is associated with short-term functional outcome of acute ischemic stroke: A prospective cohort study
title_full Visinin-like protein-1 level is associated with short-term functional outcome of acute ischemic stroke: A prospective cohort study
title_fullStr Visinin-like protein-1 level is associated with short-term functional outcome of acute ischemic stroke: A prospective cohort study
title_full_unstemmed Visinin-like protein-1 level is associated with short-term functional outcome of acute ischemic stroke: A prospective cohort study
title_short Visinin-like protein-1 level is associated with short-term functional outcome of acute ischemic stroke: A prospective cohort study
title_sort visinin-like protein-1 level is associated with short-term functional outcome of acute ischemic stroke: a prospective cohort study
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478586/
https://www.ncbi.nlm.nih.gov/pubmed/32118731
http://dx.doi.org/10.1097/MD.0000000000019252
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