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Systemic endotoxinemia as a probable factor in reducing the treatment effectiveness of endogenous psychosis

INTRODUCTION: Inflammation is an important factor in the pathogenesis of endogenous psychosis. An inducer of inflammatory reactions can be endotoxin aggression of intestinal origin. OBJECTIVES: To determine the level of inflammation markers and indicators of systemic endotoxinemia in blood of patien...

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Autores principales: Zozulya, S., Otman, I., Oleichik, I., Anikhovskaya, I., Yakovlev, M., Klyushnik, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9475931/
http://dx.doi.org/10.1192/j.eurpsy.2021.1260
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author Zozulya, S.
Otman, I.
Oleichik, I.
Anikhovskaya, I.
Yakovlev, M.
Klyushnik, T.
author_facet Zozulya, S.
Otman, I.
Oleichik, I.
Anikhovskaya, I.
Yakovlev, M.
Klyushnik, T.
author_sort Zozulya, S.
collection PubMed
description INTRODUCTION: Inflammation is an important factor in the pathogenesis of endogenous psychosis. An inducer of inflammatory reactions can be endotoxin aggression of intestinal origin. OBJECTIVES: To determine the level of inflammation markers and indicators of systemic endotoxinemia in blood of patients with endogenous psychosis in relation to assessment of the treatment effectiveness. METHODS: 25 patients with endogenous psychosis (F20, F25) were examined before and after treatment. The control group consisted of 25 healthy people. The activity of inflammatory markers - leukocyte elastase, α1-antitrypsin, antibodies to S-100B, and indicators of systemic endotoxinemia – endotoxin concentration and antiendotoxin immunity activity were measured in blood serum. The treatment effectiveness was assessed by the dynamics of inflammatory markers. RESULTS: Based on the results of determining the studied parameters before treatment, all patients were divided into two groups. In the 1st group (6 patients, 24%), an increase of inflammatory markers activity and high concentration of endotoxin in the blood serum were revealed (p<0,001, p<0,05, respectively). In the 2nd group (19 patients, 76%), only activation of inflammatory reactions (p<0,001) was detected. After therapy in the 1st group of patients, there was no positive dynamics of all studied markers, which indicated an active course of the pathological process. In the 2nd group, the normalization of inflammatory markers was shown (p<0,05), which corresponded to the formation of remission. CONCLUSIONS: The results indicate that endotoxic aggression contributes to reduction of the effectiveness of endogenous psychosis therapy and can be considered as an additional therapeutic target.
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spelling pubmed-94759312022-09-29 Systemic endotoxinemia as a probable factor in reducing the treatment effectiveness of endogenous psychosis Zozulya, S. Otman, I. Oleichik, I. Anikhovskaya, I. Yakovlev, M. Klyushnik, T. Eur Psychiatry Abstract INTRODUCTION: Inflammation is an important factor in the pathogenesis of endogenous psychosis. An inducer of inflammatory reactions can be endotoxin aggression of intestinal origin. OBJECTIVES: To determine the level of inflammation markers and indicators of systemic endotoxinemia in blood of patients with endogenous psychosis in relation to assessment of the treatment effectiveness. METHODS: 25 patients with endogenous psychosis (F20, F25) were examined before and after treatment. The control group consisted of 25 healthy people. The activity of inflammatory markers - leukocyte elastase, α1-antitrypsin, antibodies to S-100B, and indicators of systemic endotoxinemia – endotoxin concentration and antiendotoxin immunity activity were measured in blood serum. The treatment effectiveness was assessed by the dynamics of inflammatory markers. RESULTS: Based on the results of determining the studied parameters before treatment, all patients were divided into two groups. In the 1st group (6 patients, 24%), an increase of inflammatory markers activity and high concentration of endotoxin in the blood serum were revealed (p<0,001, p<0,05, respectively). In the 2nd group (19 patients, 76%), only activation of inflammatory reactions (p<0,001) was detected. After therapy in the 1st group of patients, there was no positive dynamics of all studied markers, which indicated an active course of the pathological process. In the 2nd group, the normalization of inflammatory markers was shown (p<0,05), which corresponded to the formation of remission. CONCLUSIONS: The results indicate that endotoxic aggression contributes to reduction of the effectiveness of endogenous psychosis therapy and can be considered as an additional therapeutic target. Cambridge University Press 2021-08-13 /pmc/articles/PMC9475931/ http://dx.doi.org/10.1192/j.eurpsy.2021.1260 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Zozulya, S.
Otman, I.
Oleichik, I.
Anikhovskaya, I.
Yakovlev, M.
Klyushnik, T.
Systemic endotoxinemia as a probable factor in reducing the treatment effectiveness of endogenous psychosis
title Systemic endotoxinemia as a probable factor in reducing the treatment effectiveness of endogenous psychosis
title_full Systemic endotoxinemia as a probable factor in reducing the treatment effectiveness of endogenous psychosis
title_fullStr Systemic endotoxinemia as a probable factor in reducing the treatment effectiveness of endogenous psychosis
title_full_unstemmed Systemic endotoxinemia as a probable factor in reducing the treatment effectiveness of endogenous psychosis
title_short Systemic endotoxinemia as a probable factor in reducing the treatment effectiveness of endogenous psychosis
title_sort systemic endotoxinemia as a probable factor in reducing the treatment effectiveness of endogenous psychosis
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9475931/
http://dx.doi.org/10.1192/j.eurpsy.2021.1260
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