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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9146117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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