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Perioperative time course of matrix metalloproteinase-9 (MMP-9), its tissue inhibitor TIMP-1 & S100B protein in carotid surgery

BACKGROUND & OBJECTIVES: Ischaemic stroke is a life burdening disease for which carotid endarterectomy (CEA) is considered a gold standard intervention. Pro-inflammatory markers like matrix metalloproteinases (MMPs) and their inhibitors (TIMPs) and S-100 Beta (S100B) may have a role in the early...

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Autores principales: Nagy, Bálint, Woth, Gábor, Mérei, Ákos, Nagy, Lilla, Lantos, János, Menyhei, Gábor, Bogár, Lajos, Mühl, Diána
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859131/
https://www.ncbi.nlm.nih.gov/pubmed/27121520
http://dx.doi.org/10.4103/0971-5916.180212
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author Nagy, Bálint
Woth, Gábor
Mérei, Ákos
Nagy, Lilla
Lantos, János
Menyhei, Gábor
Bogár, Lajos
Mühl, Diána
author_facet Nagy, Bálint
Woth, Gábor
Mérei, Ákos
Nagy, Lilla
Lantos, János
Menyhei, Gábor
Bogár, Lajos
Mühl, Diána
author_sort Nagy, Bálint
collection PubMed
description BACKGROUND & OBJECTIVES: Ischaemic stroke is a life burdening disease for which carotid endarterectomy (CEA) is considered a gold standard intervention. Pro-inflammatory markers like matrix metalloproteinases (MMPs) and their inhibitors (TIMPs) and S-100 Beta (S100B) may have a role in the early inflammation and cognitive decline following CEA. This study was aimed to describe the perioperative time courses and correlations between of MMP-9, TIMP-1 and S100B following CEA. METHODS: Fifty four patients scheduled for CEA were enrolled. Blood samples were collected at four time points, T(1): preoperative, T(2): 60 min after cross-clamp release, T(3): first postoperative morning, T(4): third postoperative morning. Twenty atherosclerotic patients were included as controls. Plasma MMP-9, TIMP-1 and S100B levels were estimated by ELISA. RESULTS: TIMP-1 was decreased significantly in the CEA group (P<0.01). Plasma MMP-9 was elevated and remained elevated from T(1-4) in the CEA group (P<0.05) with a marked elevation in T(3) compared to T(1) (P<0.05). MMP-9/TIMP-1 was elevated in the CEA group and increased further by T(2) and T(3) (P<0.05). S100B was elevated on T(2) and decreased on T(3-4) compared to T(1). INTERPRETATION & CONCLUSIONS: Our study provides information on the dynamic changes of MMP-9-TIMP-1 system and S100B in the perioperative period. Preoperative reduction of TIMP-1 might be predictive for shunt requirement but future studies are required for verification.
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spelling pubmed-48591312016-05-16 Perioperative time course of matrix metalloproteinase-9 (MMP-9), its tissue inhibitor TIMP-1 & S100B protein in carotid surgery Nagy, Bálint Woth, Gábor Mérei, Ákos Nagy, Lilla Lantos, János Menyhei, Gábor Bogár, Lajos Mühl, Diána Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Ischaemic stroke is a life burdening disease for which carotid endarterectomy (CEA) is considered a gold standard intervention. Pro-inflammatory markers like matrix metalloproteinases (MMPs) and their inhibitors (TIMPs) and S-100 Beta (S100B) may have a role in the early inflammation and cognitive decline following CEA. This study was aimed to describe the perioperative time courses and correlations between of MMP-9, TIMP-1 and S100B following CEA. METHODS: Fifty four patients scheduled for CEA were enrolled. Blood samples were collected at four time points, T(1): preoperative, T(2): 60 min after cross-clamp release, T(3): first postoperative morning, T(4): third postoperative morning. Twenty atherosclerotic patients were included as controls. Plasma MMP-9, TIMP-1 and S100B levels were estimated by ELISA. RESULTS: TIMP-1 was decreased significantly in the CEA group (P<0.01). Plasma MMP-9 was elevated and remained elevated from T(1-4) in the CEA group (P<0.05) with a marked elevation in T(3) compared to T(1) (P<0.05). MMP-9/TIMP-1 was elevated in the CEA group and increased further by T(2) and T(3) (P<0.05). S100B was elevated on T(2) and decreased on T(3-4) compared to T(1). INTERPRETATION & CONCLUSIONS: Our study provides information on the dynamic changes of MMP-9-TIMP-1 system and S100B in the perioperative period. Preoperative reduction of TIMP-1 might be predictive for shunt requirement but future studies are required for verification. Medknow Publications & Media Pvt Ltd 2016-02 /pmc/articles/PMC4859131/ /pubmed/27121520 http://dx.doi.org/10.4103/0971-5916.180212 Text en Copyright: © Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Nagy, Bálint
Woth, Gábor
Mérei, Ákos
Nagy, Lilla
Lantos, János
Menyhei, Gábor
Bogár, Lajos
Mühl, Diána
Perioperative time course of matrix metalloproteinase-9 (MMP-9), its tissue inhibitor TIMP-1 & S100B protein in carotid surgery
title Perioperative time course of matrix metalloproteinase-9 (MMP-9), its tissue inhibitor TIMP-1 & S100B protein in carotid surgery
title_full Perioperative time course of matrix metalloproteinase-9 (MMP-9), its tissue inhibitor TIMP-1 & S100B protein in carotid surgery
title_fullStr Perioperative time course of matrix metalloproteinase-9 (MMP-9), its tissue inhibitor TIMP-1 & S100B protein in carotid surgery
title_full_unstemmed Perioperative time course of matrix metalloproteinase-9 (MMP-9), its tissue inhibitor TIMP-1 & S100B protein in carotid surgery
title_short Perioperative time course of matrix metalloproteinase-9 (MMP-9), its tissue inhibitor TIMP-1 & S100B protein in carotid surgery
title_sort perioperative time course of matrix metalloproteinase-9 (mmp-9), its tissue inhibitor timp-1 & s100b protein in carotid surgery
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859131/
https://www.ncbi.nlm.nih.gov/pubmed/27121520
http://dx.doi.org/10.4103/0971-5916.180212
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