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I-FABP is decreased in COVID-19 patients, independently of the prognosis
BACKGROUND: Severe acute respiratory syndrome caused by the novel coronavirus (SARS-CoV-2) is frequently associated with gastrointestinal manifestations. Herein we evaluated the interest in measuring the intestinal fatty acid-binding protein (I-FABP), a biomarker of intestinal injury, in COVID-19 pa...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049236/ https://www.ncbi.nlm.nih.gov/pubmed/33857216 http://dx.doi.org/10.1371/journal.pone.0249799 |
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author | Guedj, Kevin Uzzan, Mathieu Soudan, Damien Trichet, Catherine Nicoletti, Antonino Weiss, Emmanuel Manceau, Hana Nuzzo, Alexandre Corcos, Olivier Treton, Xavier Peoc’h, Katell |
author_facet | Guedj, Kevin Uzzan, Mathieu Soudan, Damien Trichet, Catherine Nicoletti, Antonino Weiss, Emmanuel Manceau, Hana Nuzzo, Alexandre Corcos, Olivier Treton, Xavier Peoc’h, Katell |
author_sort | Guedj, Kevin |
collection | PubMed |
description | BACKGROUND: Severe acute respiratory syndrome caused by the novel coronavirus (SARS-CoV-2) is frequently associated with gastrointestinal manifestations. Herein we evaluated the interest in measuring the intestinal fatty acid-binding protein (I-FABP), a biomarker of intestinal injury, in COVID-19 patients. METHODS: Serum I-FABP was analyzed in 28 consecutive patients hospitalized for a PCR-confirmed COVID-19, in 24 hospitalized patients with non-COVID-19 pulmonary diseases, and 79 patients admitted to the emergency room for abdominal pain. RESULTS: I-FABP serum concentrations were significantly lower in patients with COVID-19, as compared to patients with non-COVID-19 pulmonary diseases [70.3 pg/mL (47–167.9) vs. 161.1 pg/mL (88.98–305.2), respectively, p = 0.008]. I-FABP concentrations in these two populations were significantly lower than in patients with abdominal pain without COVID-19 [344.8 pg/mL (268.9–579.6)]. I-FABP was neither associated with severity nor the duration of symptoms. I-FABP was correlated with polymorphonuclear cell counts. CONCLUSIONS: In this pilot study, we observed a low I-FABP concentration in COVID-19 patients either with or without gastrointestinal symptoms, of which the pathophysiological mechanisms and clinical impact remain to be established. Further explorations on a larger cohort of patients will be needed to unravel the molecular mechanism of such observation, including the effects of malabsorption and/or abnormal lipid metabolism. |
format | Online Article Text |
id | pubmed-8049236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-80492362021-04-21 I-FABP is decreased in COVID-19 patients, independently of the prognosis Guedj, Kevin Uzzan, Mathieu Soudan, Damien Trichet, Catherine Nicoletti, Antonino Weiss, Emmanuel Manceau, Hana Nuzzo, Alexandre Corcos, Olivier Treton, Xavier Peoc’h, Katell PLoS One Research Article BACKGROUND: Severe acute respiratory syndrome caused by the novel coronavirus (SARS-CoV-2) is frequently associated with gastrointestinal manifestations. Herein we evaluated the interest in measuring the intestinal fatty acid-binding protein (I-FABP), a biomarker of intestinal injury, in COVID-19 patients. METHODS: Serum I-FABP was analyzed in 28 consecutive patients hospitalized for a PCR-confirmed COVID-19, in 24 hospitalized patients with non-COVID-19 pulmonary diseases, and 79 patients admitted to the emergency room for abdominal pain. RESULTS: I-FABP serum concentrations were significantly lower in patients with COVID-19, as compared to patients with non-COVID-19 pulmonary diseases [70.3 pg/mL (47–167.9) vs. 161.1 pg/mL (88.98–305.2), respectively, p = 0.008]. I-FABP concentrations in these two populations were significantly lower than in patients with abdominal pain without COVID-19 [344.8 pg/mL (268.9–579.6)]. I-FABP was neither associated with severity nor the duration of symptoms. I-FABP was correlated with polymorphonuclear cell counts. CONCLUSIONS: In this pilot study, we observed a low I-FABP concentration in COVID-19 patients either with or without gastrointestinal symptoms, of which the pathophysiological mechanisms and clinical impact remain to be established. Further explorations on a larger cohort of patients will be needed to unravel the molecular mechanism of such observation, including the effects of malabsorption and/or abnormal lipid metabolism. Public Library of Science 2021-04-15 /pmc/articles/PMC8049236/ /pubmed/33857216 http://dx.doi.org/10.1371/journal.pone.0249799 Text en © 2021 Guedj et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Guedj, Kevin Uzzan, Mathieu Soudan, Damien Trichet, Catherine Nicoletti, Antonino Weiss, Emmanuel Manceau, Hana Nuzzo, Alexandre Corcos, Olivier Treton, Xavier Peoc’h, Katell I-FABP is decreased in COVID-19 patients, independently of the prognosis |
title | I-FABP is decreased in COVID-19 patients, independently of the prognosis |
title_full | I-FABP is decreased in COVID-19 patients, independently of the prognosis |
title_fullStr | I-FABP is decreased in COVID-19 patients, independently of the prognosis |
title_full_unstemmed | I-FABP is decreased in COVID-19 patients, independently of the prognosis |
title_short | I-FABP is decreased in COVID-19 patients, independently of the prognosis |
title_sort | i-fabp is decreased in covid-19 patients, independently of the prognosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049236/ https://www.ncbi.nlm.nih.gov/pubmed/33857216 http://dx.doi.org/10.1371/journal.pone.0249799 |
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