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Plasmatic Oxidative and Metabonomic Profile of Patients with Different Degrees of Biliary Acute Pancreatitis Severity
Acute pancreatitis (AP) is an inflammatory process of the pancreas with variable involvement of the pancreatic and peripancreatic tissues and remote organ systems. The main goal of this study was to evaluate the inflammatory biomarkers, oxidative stress (OS), and plasma metabolome of patients with d...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234183/ https://www.ncbi.nlm.nih.gov/pubmed/34205667 http://dx.doi.org/10.3390/antiox10060988 |
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author | Silva-Vaz, Pedro Jarak, Ivana Rato, Luís Oliveira, Pedro F. Morgado-Nunes, Sara Paulino, Aida Castelo-Branco, Miguel Botelho, Maria Filomena Tralhão, José Guilherme Alves, Marco G. Abrantes, Ana Margarida |
author_facet | Silva-Vaz, Pedro Jarak, Ivana Rato, Luís Oliveira, Pedro F. Morgado-Nunes, Sara Paulino, Aida Castelo-Branco, Miguel Botelho, Maria Filomena Tralhão, José Guilherme Alves, Marco G. Abrantes, Ana Margarida |
author_sort | Silva-Vaz, Pedro |
collection | PubMed |
description | Acute pancreatitis (AP) is an inflammatory process of the pancreas with variable involvement of the pancreatic and peripancreatic tissues and remote organ systems. The main goal of this study was to evaluate the inflammatory biomarkers, oxidative stress (OS), and plasma metabolome of patients with different degrees of biliary AP severity to improve its prognosis. Twenty-nine patients with biliary AP and 11 healthy controls were enrolled in this study. We analyzed several inflammatory biomarkers, multifactorial scores, reactive oxygen species (ROS), antioxidants defenses, and the plasma metabolome of biliary AP and healthy controls. Hepcidin (1.00), CRP (0.94), and SIRI (0.87) were the most accurate serological biomarkers of AP severity. OS played a pivotal role in the initial phase of AP, with significant changes in ROS and antioxidant defenses relating to AP severity. Phenylalanine (p < 0.05), threonine (p < 0.05), and lipids (p < 0.01) showed significant changes in AP severity. The role of hepcidin and SIRI were confirmed as new prognostic biomarkers of biliary AP. OS appears to have a role in the onset and progression of the AP process. Overall, this study identified several metabolites that may predict the onset and progression of biliary AP severity, constituting the first metabonomic study in the field of biliary AP. |
format | Online Article Text |
id | pubmed-8234183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82341832021-06-27 Plasmatic Oxidative and Metabonomic Profile of Patients with Different Degrees of Biliary Acute Pancreatitis Severity Silva-Vaz, Pedro Jarak, Ivana Rato, Luís Oliveira, Pedro F. Morgado-Nunes, Sara Paulino, Aida Castelo-Branco, Miguel Botelho, Maria Filomena Tralhão, José Guilherme Alves, Marco G. Abrantes, Ana Margarida Antioxidants (Basel) Article Acute pancreatitis (AP) is an inflammatory process of the pancreas with variable involvement of the pancreatic and peripancreatic tissues and remote organ systems. The main goal of this study was to evaluate the inflammatory biomarkers, oxidative stress (OS), and plasma metabolome of patients with different degrees of biliary AP severity to improve its prognosis. Twenty-nine patients with biliary AP and 11 healthy controls were enrolled in this study. We analyzed several inflammatory biomarkers, multifactorial scores, reactive oxygen species (ROS), antioxidants defenses, and the plasma metabolome of biliary AP and healthy controls. Hepcidin (1.00), CRP (0.94), and SIRI (0.87) were the most accurate serological biomarkers of AP severity. OS played a pivotal role in the initial phase of AP, with significant changes in ROS and antioxidant defenses relating to AP severity. Phenylalanine (p < 0.05), threonine (p < 0.05), and lipids (p < 0.01) showed significant changes in AP severity. The role of hepcidin and SIRI were confirmed as new prognostic biomarkers of biliary AP. OS appears to have a role in the onset and progression of the AP process. Overall, this study identified several metabolites that may predict the onset and progression of biliary AP severity, constituting the first metabonomic study in the field of biliary AP. MDPI 2021-06-21 /pmc/articles/PMC8234183/ /pubmed/34205667 http://dx.doi.org/10.3390/antiox10060988 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Silva-Vaz, Pedro Jarak, Ivana Rato, Luís Oliveira, Pedro F. Morgado-Nunes, Sara Paulino, Aida Castelo-Branco, Miguel Botelho, Maria Filomena Tralhão, José Guilherme Alves, Marco G. Abrantes, Ana Margarida Plasmatic Oxidative and Metabonomic Profile of Patients with Different Degrees of Biliary Acute Pancreatitis Severity |
title | Plasmatic Oxidative and Metabonomic Profile of Patients with Different Degrees of Biliary Acute Pancreatitis Severity |
title_full | Plasmatic Oxidative and Metabonomic Profile of Patients with Different Degrees of Biliary Acute Pancreatitis Severity |
title_fullStr | Plasmatic Oxidative and Metabonomic Profile of Patients with Different Degrees of Biliary Acute Pancreatitis Severity |
title_full_unstemmed | Plasmatic Oxidative and Metabonomic Profile of Patients with Different Degrees of Biliary Acute Pancreatitis Severity |
title_short | Plasmatic Oxidative and Metabonomic Profile of Patients with Different Degrees of Biliary Acute Pancreatitis Severity |
title_sort | plasmatic oxidative and metabonomic profile of patients with different degrees of biliary acute pancreatitis severity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234183/ https://www.ncbi.nlm.nih.gov/pubmed/34205667 http://dx.doi.org/10.3390/antiox10060988 |
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