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Circulating miRNA-195-5p and -451a in Patients with Acute Hemorrhagic Stroke in Emergency Department

(1) Background: In our previous study, acute ischemic stroke (AIS) patients showed increased levels of circulating miRNAs (-195-5p and -451a) involved in vascular endothelial growth factor A (VEGF-A) regulation. Here, we evaluated, for the first time, both circulating miRNAs in acute intracerebral h...

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Autores principales: Giordano, Mauro, Trotta, Maria Consiglia, Ciarambino, Tiziana, D’Amico, Michele, Schettini, Federico, Sisto, Angela Di, D’Auria, Valentina, Voza, Antonio, Malatino, Lorenzo Salvatore, Biolo, Gianni, Mearelli, Filippo, Franceschi, Francesco, Paolisso, Giuseppe, Adinolfi, Luigi Elio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146117/
https://www.ncbi.nlm.nih.gov/pubmed/35629429
http://dx.doi.org/10.3390/life12050763
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author Giordano, Mauro
Trotta, Maria Consiglia
Ciarambino, Tiziana
D’Amico, Michele
Schettini, Federico
Sisto, Angela Di
D’Auria, Valentina
Voza, Antonio
Malatino, Lorenzo Salvatore
Biolo, Gianni
Mearelli, Filippo
Franceschi, Francesco
Paolisso, Giuseppe
Adinolfi, Luigi Elio
author_facet Giordano, Mauro
Trotta, Maria Consiglia
Ciarambino, Tiziana
D’Amico, Michele
Schettini, Federico
Sisto, Angela Di
D’Auria, Valentina
Voza, Antonio
Malatino, Lorenzo Salvatore
Biolo, Gianni
Mearelli, Filippo
Franceschi, Francesco
Paolisso, Giuseppe
Adinolfi, Luigi Elio
author_sort Giordano, Mauro
collection PubMed
description (1) Background: In our previous study, acute ischemic stroke (AIS) patients showed increased levels of circulating miRNAs (-195-5p and -451a) involved in vascular endothelial growth factor A (VEGF-A) regulation. Here, we evaluated, for the first time, both circulating miRNAs in acute intracerebral hemorrhagic (ICH) patients. (2) Methods: Circulating miRNAs and serum VEGF-A were assessed by real-time PCR and ELISA in 20 acute ICH, 21 AIS patients, and 21 controls. These were evaluated at hospital admission (T0) and after 96 h (T96) from admission. (3) Results: At T0, circulating miRNAs were five-times up-regulated in AIS patients, tending to decrease at T96. By contrast, in the acute ICH group, circulating miRNAs were significantly increased at both T0 and T96. Moreover, a significant decrease was observed in serum VEGF-A levels at T0 in AIS patients, tending to increase at T96. Conversely, in acute ICH patients, the levels of VEGF-A were significantly decreased at both T0 and T96. (4) Conclusions: The absence of a reduction in circulating miRNAs (195-5p and -451a), reported in acute ICH subjects after 96 h from hospital admission, together with the absence of increment of serum VEGF-A, may represent useful biomarkers indicating the severe brain damage status that characterizes acute ICH patients.
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spelling pubmed-91461172022-05-29 Circulating miRNA-195-5p and -451a in Patients with Acute Hemorrhagic Stroke in Emergency Department Giordano, Mauro Trotta, Maria Consiglia Ciarambino, Tiziana D’Amico, Michele Schettini, Federico Sisto, Angela Di D’Auria, Valentina Voza, Antonio Malatino, Lorenzo Salvatore Biolo, Gianni Mearelli, Filippo Franceschi, Francesco Paolisso, Giuseppe Adinolfi, Luigi Elio Life (Basel) Article (1) Background: In our previous study, acute ischemic stroke (AIS) patients showed increased levels of circulating miRNAs (-195-5p and -451a) involved in vascular endothelial growth factor A (VEGF-A) regulation. Here, we evaluated, for the first time, both circulating miRNAs in acute intracerebral hemorrhagic (ICH) patients. (2) Methods: Circulating miRNAs and serum VEGF-A were assessed by real-time PCR and ELISA in 20 acute ICH, 21 AIS patients, and 21 controls. These were evaluated at hospital admission (T0) and after 96 h (T96) from admission. (3) Results: At T0, circulating miRNAs were five-times up-regulated in AIS patients, tending to decrease at T96. By contrast, in the acute ICH group, circulating miRNAs were significantly increased at both T0 and T96. Moreover, a significant decrease was observed in serum VEGF-A levels at T0 in AIS patients, tending to increase at T96. Conversely, in acute ICH patients, the levels of VEGF-A were significantly decreased at both T0 and T96. (4) Conclusions: The absence of a reduction in circulating miRNAs (195-5p and -451a), reported in acute ICH subjects after 96 h from hospital admission, together with the absence of increment of serum VEGF-A, may represent useful biomarkers indicating the severe brain damage status that characterizes acute ICH patients. MDPI 2022-05-21 /pmc/articles/PMC9146117/ /pubmed/35629429 http://dx.doi.org/10.3390/life12050763 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Giordano, Mauro
Trotta, Maria Consiglia
Ciarambino, Tiziana
D’Amico, Michele
Schettini, Federico
Sisto, Angela Di
D’Auria, Valentina
Voza, Antonio
Malatino, Lorenzo Salvatore
Biolo, Gianni
Mearelli, Filippo
Franceschi, Francesco
Paolisso, Giuseppe
Adinolfi, Luigi Elio
Circulating miRNA-195-5p and -451a in Patients with Acute Hemorrhagic Stroke in Emergency Department
title Circulating miRNA-195-5p and -451a in Patients with Acute Hemorrhagic Stroke in Emergency Department
title_full Circulating miRNA-195-5p and -451a in Patients with Acute Hemorrhagic Stroke in Emergency Department
title_fullStr Circulating miRNA-195-5p and -451a in Patients with Acute Hemorrhagic Stroke in Emergency Department
title_full_unstemmed Circulating miRNA-195-5p and -451a in Patients with Acute Hemorrhagic Stroke in Emergency Department
title_short Circulating miRNA-195-5p and -451a in Patients with Acute Hemorrhagic Stroke in Emergency Department
title_sort circulating mirna-195-5p and -451a in patients with acute hemorrhagic stroke in emergency department
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146117/
https://www.ncbi.nlm.nih.gov/pubmed/35629429
http://dx.doi.org/10.3390/life12050763
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