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Poor expression of miR‐195‐5p can assist the diagnosis of cerebral vasospasm after subarachnoid hemorrhage and predict adverse outcomes

OBJECTIVE: Patients with spontaneous subarachnoid hemorrhage (SAH) may develop refractory arterial cerebral vasospasm (CVS), which is the leading cause of death in SAH patients. This study explored the clinical diagnostic value of serum miR‐195‐5p levels in CVS after SAH (SAH + CVS) and its relation...

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Autores principales: Li, Yong, Yang, Senyuan, Zhou, Xiaobin, Lai, Runlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9759123/
https://www.ncbi.nlm.nih.gov/pubmed/36350075
http://dx.doi.org/10.1002/brb3.2766
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author Li, Yong
Yang, Senyuan
Zhou, Xiaobin
Lai, Runlong
author_facet Li, Yong
Yang, Senyuan
Zhou, Xiaobin
Lai, Runlong
author_sort Li, Yong
collection PubMed
description OBJECTIVE: Patients with spontaneous subarachnoid hemorrhage (SAH) may develop refractory arterial cerebral vasospasm (CVS), which is the leading cause of death in SAH patients. This study explored the clinical diagnostic value of serum miR‐195‐5p levels in CVS after SAH (SAH + CVS) and its relationship with the prognosis of SAH + CVS. METHODS: A total of 110 patients with spontaneous SAH were divided into the SAH group (N = 62) and SAH + CVS group (N = 58), with 60 healthy subjects as controls. The clinical data of blood glucose, blood sodium fluctuation, and serum lactic acid were recorded. miR‐195‐5p serum level was detected by RT‐qPCR and its diagnostic value on SAH + CVS was analyzed by receiver operating characteristic curve. Serum levels of PDGF/IL‐6/ET‐1 and their correlation with miR‐195‐5p were analyzed using RT‐qPCR, enzyme‐linked immunosorbent assay, and Pearson's method. The patient prognosis was evaluated by Glasgow Outcome Scale. The effect of miR‐195‐5p levels on adverse prognosis was analyzed by Kaplan‐Meier method and Cox regression analysis. RESULTS: miR‐195‐5p was lowly expressed in the serum of SAH patients and lower in SAH + CVS patients. Serum miR‐195‐5p level assisted the diagnosis of SAH and SAH + CVS and was negatively correlated with PDGF/IL‐6/ET‐1 levels and was an independent risk factor together with ET‐1 and blood glucose for SAH + CVS. miR‐195‐5p low expression predicted a higher cumulative incidence of adverse outcomes and was an independent predictor of adverse outcomes. CONCLUSION: Poor expression of miR‐195‐5p can assist the diagnosis of SAH + CVS and predict higher adverse outcomes.
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spelling pubmed-97591232022-12-20 Poor expression of miR‐195‐5p can assist the diagnosis of cerebral vasospasm after subarachnoid hemorrhage and predict adverse outcomes Li, Yong Yang, Senyuan Zhou, Xiaobin Lai, Runlong Brain Behav Original Articles OBJECTIVE: Patients with spontaneous subarachnoid hemorrhage (SAH) may develop refractory arterial cerebral vasospasm (CVS), which is the leading cause of death in SAH patients. This study explored the clinical diagnostic value of serum miR‐195‐5p levels in CVS after SAH (SAH + CVS) and its relationship with the prognosis of SAH + CVS. METHODS: A total of 110 patients with spontaneous SAH were divided into the SAH group (N = 62) and SAH + CVS group (N = 58), with 60 healthy subjects as controls. The clinical data of blood glucose, blood sodium fluctuation, and serum lactic acid were recorded. miR‐195‐5p serum level was detected by RT‐qPCR and its diagnostic value on SAH + CVS was analyzed by receiver operating characteristic curve. Serum levels of PDGF/IL‐6/ET‐1 and their correlation with miR‐195‐5p were analyzed using RT‐qPCR, enzyme‐linked immunosorbent assay, and Pearson's method. The patient prognosis was evaluated by Glasgow Outcome Scale. The effect of miR‐195‐5p levels on adverse prognosis was analyzed by Kaplan‐Meier method and Cox regression analysis. RESULTS: miR‐195‐5p was lowly expressed in the serum of SAH patients and lower in SAH + CVS patients. Serum miR‐195‐5p level assisted the diagnosis of SAH and SAH + CVS and was negatively correlated with PDGF/IL‐6/ET‐1 levels and was an independent risk factor together with ET‐1 and blood glucose for SAH + CVS. miR‐195‐5p low expression predicted a higher cumulative incidence of adverse outcomes and was an independent predictor of adverse outcomes. CONCLUSION: Poor expression of miR‐195‐5p can assist the diagnosis of SAH + CVS and predict higher adverse outcomes. John Wiley and Sons Inc. 2022-11-09 /pmc/articles/PMC9759123/ /pubmed/36350075 http://dx.doi.org/10.1002/brb3.2766 Text en © 2022 The Authors. Brain and Behavior published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Li, Yong
Yang, Senyuan
Zhou, Xiaobin
Lai, Runlong
Poor expression of miR‐195‐5p can assist the diagnosis of cerebral vasospasm after subarachnoid hemorrhage and predict adverse outcomes
title Poor expression of miR‐195‐5p can assist the diagnosis of cerebral vasospasm after subarachnoid hemorrhage and predict adverse outcomes
title_full Poor expression of miR‐195‐5p can assist the diagnosis of cerebral vasospasm after subarachnoid hemorrhage and predict adverse outcomes
title_fullStr Poor expression of miR‐195‐5p can assist the diagnosis of cerebral vasospasm after subarachnoid hemorrhage and predict adverse outcomes
title_full_unstemmed Poor expression of miR‐195‐5p can assist the diagnosis of cerebral vasospasm after subarachnoid hemorrhage and predict adverse outcomes
title_short Poor expression of miR‐195‐5p can assist the diagnosis of cerebral vasospasm after subarachnoid hemorrhage and predict adverse outcomes
title_sort poor expression of mir‐195‐5p can assist the diagnosis of cerebral vasospasm after subarachnoid hemorrhage and predict adverse outcomes
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9759123/
https://www.ncbi.nlm.nih.gov/pubmed/36350075
http://dx.doi.org/10.1002/brb3.2766
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