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Histidine-rich glycoprotein as a prognostic biomarker for sepsis
Various biomarkers have been proposed for sepsis; however, only a few become the standard. We previously reported that plasma histidine-rich glycoprotein (HRG) levels decreased in septic mice, and supplemental infusion of HRG improved survival in mice model of sepsis. Moreover, our previous clinical...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119687/ https://www.ncbi.nlm.nih.gov/pubmed/33986340 http://dx.doi.org/10.1038/s41598-021-89555-z |
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author | Kuroda, Kosuke Ishii, Kenzo Mihara, Yuko Kawanoue, Naoya Wake, Hidenori Mori, Shuji Yoshida, Michihiro Nishibori, Masahiro Morimatsu, Hiroshi |
author_facet | Kuroda, Kosuke Ishii, Kenzo Mihara, Yuko Kawanoue, Naoya Wake, Hidenori Mori, Shuji Yoshida, Michihiro Nishibori, Masahiro Morimatsu, Hiroshi |
author_sort | Kuroda, Kosuke |
collection | PubMed |
description | Various biomarkers have been proposed for sepsis; however, only a few become the standard. We previously reported that plasma histidine-rich glycoprotein (HRG) levels decreased in septic mice, and supplemental infusion of HRG improved survival in mice model of sepsis. Moreover, our previous clinical study demonstrated that HRG levels in septic patients were lower than those in noninfective systemic inflammatory response syndrome patients, and it could be a biomarker for sepsis. In this study, we focused on septic patients and assessed the differences in HRG levels between the non-survivors and survivors. We studied ICU patients newly diagnosed with sepsis. Blood samples were collected within 24 h of ICU admission, and HRG levels were determined using an enzyme-linked immunosorbent assay. Ninety-nine septic patients from 11 institutes in Japan were included. HRG levels were significantly lower in non-survivors (n = 16) than in survivors (n = 83) (median, 15.1 [interquartile ranges, 12.7–16.6] vs. 30.6 [22.1–39.6] µg/ml; p < 0.01). Survival analysis revealed that HRG levels were associated with mortality (hazard ratio 0.79, p < 0.01), and the Harrell C-index (predictive power) for HRG was 0.90. These results suggested that HRG could be a novel prognostic biomarker for sepsis. |
format | Online Article Text |
id | pubmed-8119687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81196872021-05-17 Histidine-rich glycoprotein as a prognostic biomarker for sepsis Kuroda, Kosuke Ishii, Kenzo Mihara, Yuko Kawanoue, Naoya Wake, Hidenori Mori, Shuji Yoshida, Michihiro Nishibori, Masahiro Morimatsu, Hiroshi Sci Rep Article Various biomarkers have been proposed for sepsis; however, only a few become the standard. We previously reported that plasma histidine-rich glycoprotein (HRG) levels decreased in septic mice, and supplemental infusion of HRG improved survival in mice model of sepsis. Moreover, our previous clinical study demonstrated that HRG levels in septic patients were lower than those in noninfective systemic inflammatory response syndrome patients, and it could be a biomarker for sepsis. In this study, we focused on septic patients and assessed the differences in HRG levels between the non-survivors and survivors. We studied ICU patients newly diagnosed with sepsis. Blood samples were collected within 24 h of ICU admission, and HRG levels were determined using an enzyme-linked immunosorbent assay. Ninety-nine septic patients from 11 institutes in Japan were included. HRG levels were significantly lower in non-survivors (n = 16) than in survivors (n = 83) (median, 15.1 [interquartile ranges, 12.7–16.6] vs. 30.6 [22.1–39.6] µg/ml; p < 0.01). Survival analysis revealed that HRG levels were associated with mortality (hazard ratio 0.79, p < 0.01), and the Harrell C-index (predictive power) for HRG was 0.90. These results suggested that HRG could be a novel prognostic biomarker for sepsis. Nature Publishing Group UK 2021-05-13 /pmc/articles/PMC8119687/ /pubmed/33986340 http://dx.doi.org/10.1038/s41598-021-89555-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kuroda, Kosuke Ishii, Kenzo Mihara, Yuko Kawanoue, Naoya Wake, Hidenori Mori, Shuji Yoshida, Michihiro Nishibori, Masahiro Morimatsu, Hiroshi Histidine-rich glycoprotein as a prognostic biomarker for sepsis |
title | Histidine-rich glycoprotein as a prognostic biomarker for sepsis |
title_full | Histidine-rich glycoprotein as a prognostic biomarker for sepsis |
title_fullStr | Histidine-rich glycoprotein as a prognostic biomarker for sepsis |
title_full_unstemmed | Histidine-rich glycoprotein as a prognostic biomarker for sepsis |
title_short | Histidine-rich glycoprotein as a prognostic biomarker for sepsis |
title_sort | histidine-rich glycoprotein as a prognostic biomarker for sepsis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119687/ https://www.ncbi.nlm.nih.gov/pubmed/33986340 http://dx.doi.org/10.1038/s41598-021-89555-z |
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