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Inflammatory and oxidative stress markers in intracerebral hemorrhage: Relevance as prognostic markers for quantification of the edema volume

We aimed to analyze the inflammatory and oxidative stress (OS) markers after intracerebral hemorrhage (ICH) and their temporal changes, interaction effects, and prognostic values as biomarkers for the prediction of the edema volume. Our prospective, longitudinal study included a cohort group of 73 c...

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Autores principales: Rendevski, Vladimir, Aleksovski, Boris, Mihajlovska Rendevska, Ana, Hadzi‐Petrushev, Nikola, Manusheva, Nensi, Shuntov, Blagoj, Gjorgoski, Icko
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/PMC10041164/
https://www.ncbi.nlm.nih.gov/pubmed/35762501
http://dx.doi.org/10.1111/bpa.13106
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author Rendevski, Vladimir
Aleksovski, Boris
Mihajlovska Rendevska, Ana
Hadzi‐Petrushev, Nikola
Manusheva, Nensi
Shuntov, Blagoj
Gjorgoski, Icko
author_facet Rendevski, Vladimir
Aleksovski, Boris
Mihajlovska Rendevska, Ana
Hadzi‐Petrushev, Nikola
Manusheva, Nensi
Shuntov, Blagoj
Gjorgoski, Icko
author_sort Rendevski, Vladimir
collection PubMed
description We aimed to analyze the inflammatory and oxidative stress (OS) markers after intracerebral hemorrhage (ICH) and their temporal changes, interaction effects, and prognostic values as biomarkers for the prediction of the edema volume. Our prospective, longitudinal study included a cohort group of 73 conservatively treated patients with ICH, without hematoma expansion or intraventricular bleeding, which were initialized with the same treatment and provided with the same in‐hospital care during the disease course. Study procedures included multilevel comprehensive analyses of clinical and neuroimaging data, aligned with the exploration of 19 inflammatory and five OS markers. White blood cells (WBC), C‐reactive protein (CRP), erythrocyte sedimentation rate (ESR), neutrophilia, and lymphopenia peaked 3 days post‐ICH, and they showed much stronger correlations with clinical and neuroimaging variables, when compared to the admission values. An intricate interplay among inflammatory (WBC, CRP, neutrophils, neutrophil‐to‐lymphocyte ratio [NLR], interleukin (IL)‐6, and IL‐10) and OS mechanisms (catalase activity and advanced oxidation protein products [AOPP]) was detected operating 3‐days post‐ICH, being assessed as relevant for prediction of the edema. The overall results suggested complex pathology of formation of post‐ICH edema, via: (A) Not additive, but statistically significant synergistic interactions between CRP‐ESR, neutrophils‐CRP, and neutrophils‐IL‐6 as drivers for the edema formation; (B) Significant antagonistic effect of high protein oxidation on the CRP‐edema dependence, suggesting a mechanism of potential OS‐CRP negative feedback loop and redox inactivation of CRP. The final multiple regression model separated the third‐day variables NLR, CRP × AOPP, and WBC, as significant prognostic biomarkers for the prediction of the edema volume, with NLR being associated with the highest effect size. Our developed mathematical equation with 3D modeling for prediction and quantification of the edema volume might be beneficial for taking timely adequate strategies for prevention of delayed neurological deteriorations.
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spelling pubmed-100411642023-03-28 Inflammatory and oxidative stress markers in intracerebral hemorrhage: Relevance as prognostic markers for quantification of the edema volume Rendevski, Vladimir Aleksovski, Boris Mihajlovska Rendevska, Ana Hadzi‐Petrushev, Nikola Manusheva, Nensi Shuntov, Blagoj Gjorgoski, Icko Brain Pathol Research Articles We aimed to analyze the inflammatory and oxidative stress (OS) markers after intracerebral hemorrhage (ICH) and their temporal changes, interaction effects, and prognostic values as biomarkers for the prediction of the edema volume. Our prospective, longitudinal study included a cohort group of 73 conservatively treated patients with ICH, without hematoma expansion or intraventricular bleeding, which were initialized with the same treatment and provided with the same in‐hospital care during the disease course. Study procedures included multilevel comprehensive analyses of clinical and neuroimaging data, aligned with the exploration of 19 inflammatory and five OS markers. White blood cells (WBC), C‐reactive protein (CRP), erythrocyte sedimentation rate (ESR), neutrophilia, and lymphopenia peaked 3 days post‐ICH, and they showed much stronger correlations with clinical and neuroimaging variables, when compared to the admission values. An intricate interplay among inflammatory (WBC, CRP, neutrophils, neutrophil‐to‐lymphocyte ratio [NLR], interleukin (IL)‐6, and IL‐10) and OS mechanisms (catalase activity and advanced oxidation protein products [AOPP]) was detected operating 3‐days post‐ICH, being assessed as relevant for prediction of the edema. The overall results suggested complex pathology of formation of post‐ICH edema, via: (A) Not additive, but statistically significant synergistic interactions between CRP‐ESR, neutrophils‐CRP, and neutrophils‐IL‐6 as drivers for the edema formation; (B) Significant antagonistic effect of high protein oxidation on the CRP‐edema dependence, suggesting a mechanism of potential OS‐CRP negative feedback loop and redox inactivation of CRP. The final multiple regression model separated the third‐day variables NLR, CRP × AOPP, and WBC, as significant prognostic biomarkers for the prediction of the edema volume, with NLR being associated with the highest effect size. Our developed mathematical equation with 3D modeling for prediction and quantification of the edema volume might be beneficial for taking timely adequate strategies for prevention of delayed neurological deteriorations. John Wiley and Sons Inc. 2022-06-28 /pmc/articles/PMC10041164/ /pubmed/35762501 http://dx.doi.org/10.1111/bpa.13106 Text en © 2022 The Authors. Brain Pathology published by John Wiley & Sons Ltd on behalf of International Society of Neuropathology. 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 Research Articles
Rendevski, Vladimir
Aleksovski, Boris
Mihajlovska Rendevska, Ana
Hadzi‐Petrushev, Nikola
Manusheva, Nensi
Shuntov, Blagoj
Gjorgoski, Icko
Inflammatory and oxidative stress markers in intracerebral hemorrhage: Relevance as prognostic markers for quantification of the edema volume
title Inflammatory and oxidative stress markers in intracerebral hemorrhage: Relevance as prognostic markers for quantification of the edema volume
title_full Inflammatory and oxidative stress markers in intracerebral hemorrhage: Relevance as prognostic markers for quantification of the edema volume
title_fullStr Inflammatory and oxidative stress markers in intracerebral hemorrhage: Relevance as prognostic markers for quantification of the edema volume
title_full_unstemmed Inflammatory and oxidative stress markers in intracerebral hemorrhage: Relevance as prognostic markers for quantification of the edema volume
title_short Inflammatory and oxidative stress markers in intracerebral hemorrhage: Relevance as prognostic markers for quantification of the edema volume
title_sort inflammatory and oxidative stress markers in intracerebral hemorrhage: relevance as prognostic markers for quantification of the edema volume
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041164/
https://www.ncbi.nlm.nih.gov/pubmed/35762501
http://dx.doi.org/10.1111/bpa.13106
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