Cargando…

Different Biomarker Kinetics in Critically Ill Patients with High Lactate Levels

We evaluated the association of the kinetics of interleukin-6 (IL-6), neutrophil gelatinase-associated lipocalin (NGAL), and high-mobility group box 1 (HMGB1) with intensive care unit (ICU) mortality in critically ill patients with hyperlactatemia. This proof-of-concept study was conducted with pros...

Descripción completa

Detalles Bibliográficos
Autores principales: Matsuura, Ryo, Komaru, Yohei, Miyamoto, Yoshihisa, Yoshida, Teruhiko, Yoshimoto, Kohei, Hamasaki, Yoshifumi, Nangaku, Masaomi, Doi, Kent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400035/
https://www.ncbi.nlm.nih.gov/pubmed/32635454
http://dx.doi.org/10.3390/diagnostics10070454
_version_ 1783566270687346688
author Matsuura, Ryo
Komaru, Yohei
Miyamoto, Yoshihisa
Yoshida, Teruhiko
Yoshimoto, Kohei
Hamasaki, Yoshifumi
Nangaku, Masaomi
Doi, Kent
author_facet Matsuura, Ryo
Komaru, Yohei
Miyamoto, Yoshihisa
Yoshida, Teruhiko
Yoshimoto, Kohei
Hamasaki, Yoshifumi
Nangaku, Masaomi
Doi, Kent
author_sort Matsuura, Ryo
collection PubMed
description We evaluated the association of the kinetics of interleukin-6 (IL-6), neutrophil gelatinase-associated lipocalin (NGAL), and high-mobility group box 1 (HMGB1) with intensive care unit (ICU) mortality in critically ill patients with hyperlactatemia. This proof-of-concept study was conducted with prospectively enrolled patients admitted to a medical/surgical ICU with hyperlactatemia (lactate levels >4 mmol/L). Blood lactate, IL-6, NGAL, and HMGB1 were measured every 2 h until 6 h post ICU admission. The primary outcome was ICU mortality. Of thirty patients in this study, 14 patients (47%) had sepsis, and the ICU mortality was 47%. IL-6 and NGAL levels were significantly higher in septic patients than in non-septic patients. On kinetic analysis, the lactate levels were significantly decreased in survivors, and the NGAL levels were significantly increased in non-survivors. Among septic patients, a decline in IL-6 levels were observed in survivors. The HMGB1 levels were unchanged in survivors and non-survivors regardless of sepsis complication. Non-septic patients with higher reduction rate of lactate and HMGB1 had the lowest mortality than the others. ICU patients exhibited different kinetic patterns in lactate, NGAL, and IL-6, but HMGB1 did not seem to change over the 6-h duration. Further studies are necessary to evaluate the efficacy of the combination of the inflammatory biomarkers with lactate.
format Online
Article
Text
id pubmed-7400035
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-74000352020-08-23 Different Biomarker Kinetics in Critically Ill Patients with High Lactate Levels Matsuura, Ryo Komaru, Yohei Miyamoto, Yoshihisa Yoshida, Teruhiko Yoshimoto, Kohei Hamasaki, Yoshifumi Nangaku, Masaomi Doi, Kent Diagnostics (Basel) Article We evaluated the association of the kinetics of interleukin-6 (IL-6), neutrophil gelatinase-associated lipocalin (NGAL), and high-mobility group box 1 (HMGB1) with intensive care unit (ICU) mortality in critically ill patients with hyperlactatemia. This proof-of-concept study was conducted with prospectively enrolled patients admitted to a medical/surgical ICU with hyperlactatemia (lactate levels >4 mmol/L). Blood lactate, IL-6, NGAL, and HMGB1 were measured every 2 h until 6 h post ICU admission. The primary outcome was ICU mortality. Of thirty patients in this study, 14 patients (47%) had sepsis, and the ICU mortality was 47%. IL-6 and NGAL levels were significantly higher in septic patients than in non-septic patients. On kinetic analysis, the lactate levels were significantly decreased in survivors, and the NGAL levels were significantly increased in non-survivors. Among septic patients, a decline in IL-6 levels were observed in survivors. The HMGB1 levels were unchanged in survivors and non-survivors regardless of sepsis complication. Non-septic patients with higher reduction rate of lactate and HMGB1 had the lowest mortality than the others. ICU patients exhibited different kinetic patterns in lactate, NGAL, and IL-6, but HMGB1 did not seem to change over the 6-h duration. Further studies are necessary to evaluate the efficacy of the combination of the inflammatory biomarkers with lactate. MDPI 2020-07-04 /pmc/articles/PMC7400035/ /pubmed/32635454 http://dx.doi.org/10.3390/diagnostics10070454 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Matsuura, Ryo
Komaru, Yohei
Miyamoto, Yoshihisa
Yoshida, Teruhiko
Yoshimoto, Kohei
Hamasaki, Yoshifumi
Nangaku, Masaomi
Doi, Kent
Different Biomarker Kinetics in Critically Ill Patients with High Lactate Levels
title Different Biomarker Kinetics in Critically Ill Patients with High Lactate Levels
title_full Different Biomarker Kinetics in Critically Ill Patients with High Lactate Levels
title_fullStr Different Biomarker Kinetics in Critically Ill Patients with High Lactate Levels
title_full_unstemmed Different Biomarker Kinetics in Critically Ill Patients with High Lactate Levels
title_short Different Biomarker Kinetics in Critically Ill Patients with High Lactate Levels
title_sort different biomarker kinetics in critically ill patients with high lactate levels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400035/
https://www.ncbi.nlm.nih.gov/pubmed/32635454
http://dx.doi.org/10.3390/diagnostics10070454
work_keys_str_mv AT matsuuraryo differentbiomarkerkineticsincriticallyillpatientswithhighlactatelevels
AT komaruyohei differentbiomarkerkineticsincriticallyillpatientswithhighlactatelevels
AT miyamotoyoshihisa differentbiomarkerkineticsincriticallyillpatientswithhighlactatelevels
AT yoshidateruhiko differentbiomarkerkineticsincriticallyillpatientswithhighlactatelevels
AT yoshimotokohei differentbiomarkerkineticsincriticallyillpatientswithhighlactatelevels
AT hamasakiyoshifumi differentbiomarkerkineticsincriticallyillpatientswithhighlactatelevels
AT nangakumasaomi differentbiomarkerkineticsincriticallyillpatientswithhighlactatelevels
AT doikent differentbiomarkerkineticsincriticallyillpatientswithhighlactatelevels