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Association between plasma complement factor H concentration and clinical outcomes in patients with sepsis

AIM: The complement system is important for defending against pathogens, however, excessive complement activation is associated with a poor prognosis and organ dysfunction in sepsis. Complement factor H (CFH) acts to prevent excessive complement activation and damage to the self through the regulati...

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Autores principales: Shimizu, Junji, Fujino, Kazunori, Sawai, Toshihiro, Tsujita, Yasuyuki, Tabata, Takahisa, Eguchi, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814988/
https://www.ncbi.nlm.nih.gov/pubmed/33510899
http://dx.doi.org/10.1002/ams2.625
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author Shimizu, Junji
Fujino, Kazunori
Sawai, Toshihiro
Tsujita, Yasuyuki
Tabata, Takahisa
Eguchi, Yutaka
author_facet Shimizu, Junji
Fujino, Kazunori
Sawai, Toshihiro
Tsujita, Yasuyuki
Tabata, Takahisa
Eguchi, Yutaka
author_sort Shimizu, Junji
collection PubMed
description AIM: The complement system is important for defending against pathogens, however, excessive complement activation is associated with a poor prognosis and organ dysfunction in sepsis. Complement factor H (CFH) acts to prevent excessive complement activation and damage to the self through the regulation of the complement alternative pathway. We investigated the association between plasma CFH levels on admission to the intensive care unit (ICU) and 90‐day mortality, severity scores, and organ dysfunction in patients with sepsis. METHODS: We assessed the relationship between the plasma CFH on admission to the ICU and 90‐day mortality, severity scores such as the Acute Physiology and Chronic Health Evaluation II score, Sequential Organ Failure Assessment score, and Simplified Acute Physiology Score 2, and organ dysfunction. RESULTS: This analysis included 62 patients. The plasma CFH levels were significantly lower in 90‐day non‐survivors than in survivors (70.0 μg/mL [interquartile range, 51.2–97.6] versus 104.8 μg/mL [interquartile range, 66.8–124.2]; P = 0.006) . The plasma CFH levels were associated with 90‐day mortality (odds ratio 0.977; 95% confidence interval, 0.957–0.994; P = 0.01). The plasma CFH levels were negatively correlated with severity scores. The Sequential Organ Failure Assessment scores for the coagulation and neurological components were negatively correlated with the CFH concentration. CONCLUSION: Lower plasma levels of CFH were associated with increased severity and mortality in patients with sepsis on admission to the ICU and were correlated with central nervous system dysfunction and coagulopathy.
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spelling pubmed-78149882021-01-27 Association between plasma complement factor H concentration and clinical outcomes in patients with sepsis Shimizu, Junji Fujino, Kazunori Sawai, Toshihiro Tsujita, Yasuyuki Tabata, Takahisa Eguchi, Yutaka Acute Med Surg Original Articles AIM: The complement system is important for defending against pathogens, however, excessive complement activation is associated with a poor prognosis and organ dysfunction in sepsis. Complement factor H (CFH) acts to prevent excessive complement activation and damage to the self through the regulation of the complement alternative pathway. We investigated the association between plasma CFH levels on admission to the intensive care unit (ICU) and 90‐day mortality, severity scores, and organ dysfunction in patients with sepsis. METHODS: We assessed the relationship between the plasma CFH on admission to the ICU and 90‐day mortality, severity scores such as the Acute Physiology and Chronic Health Evaluation II score, Sequential Organ Failure Assessment score, and Simplified Acute Physiology Score 2, and organ dysfunction. RESULTS: This analysis included 62 patients. The plasma CFH levels were significantly lower in 90‐day non‐survivors than in survivors (70.0 μg/mL [interquartile range, 51.2–97.6] versus 104.8 μg/mL [interquartile range, 66.8–124.2]; P = 0.006) . The plasma CFH levels were associated with 90‐day mortality (odds ratio 0.977; 95% confidence interval, 0.957–0.994; P = 0.01). The plasma CFH levels were negatively correlated with severity scores. The Sequential Organ Failure Assessment scores for the coagulation and neurological components were negatively correlated with the CFH concentration. CONCLUSION: Lower plasma levels of CFH were associated with increased severity and mortality in patients with sepsis on admission to the ICU and were correlated with central nervous system dysfunction and coagulopathy. John Wiley and Sons Inc. 2021-01-19 /pmc/articles/PMC7814988/ /pubmed/33510899 http://dx.doi.org/10.1002/ams2.625 Text en © 2021 The Authors. Acute Medicine & Surgery published by John Wiley & Sons Australia, Ltd on behalf of Japanese Association for Acute Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Shimizu, Junji
Fujino, Kazunori
Sawai, Toshihiro
Tsujita, Yasuyuki
Tabata, Takahisa
Eguchi, Yutaka
Association between plasma complement factor H concentration and clinical outcomes in patients with sepsis
title Association between plasma complement factor H concentration and clinical outcomes in patients with sepsis
title_full Association between plasma complement factor H concentration and clinical outcomes in patients with sepsis
title_fullStr Association between plasma complement factor H concentration and clinical outcomes in patients with sepsis
title_full_unstemmed Association between plasma complement factor H concentration and clinical outcomes in patients with sepsis
title_short Association between plasma complement factor H concentration and clinical outcomes in patients with sepsis
title_sort association between plasma complement factor h concentration and clinical outcomes in patients with sepsis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814988/
https://www.ncbi.nlm.nih.gov/pubmed/33510899
http://dx.doi.org/10.1002/ams2.625
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