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Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19

BACKGROUND: Fatigue, sleep disturbance, and neurological symptoms during and after COVID-19 are common and might be associated with inflammation-induced changes in tryptophan (Trp) and phenylalanine (Phe) metabolism. AIM: This pilot study investigated interferon gamma inducible biochemical pathways...

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Autores principales: Gietl, Mario, Burkert, Francesco, Seiwald, Stefanie, Böhm, Anna, Hofer, Stefanie, Gostner, Johanna M, Piater, Talia, Geisler, Simon, Weiss, Guenter, Loeffler-Ragg, Judith, Sonnweber, Thomas, Tancevski, Ivan, Pizzini, Alex, Sahanic, Sabina, Fuchs, Dietmar, Bellmann-Weiler, Rosa, Kurz, Katharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076985/
https://www.ncbi.nlm.nih.gov/pubmed/37038445
http://dx.doi.org/10.1177/11786469231154244
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author Gietl, Mario
Burkert, Francesco
Seiwald, Stefanie
Böhm, Anna
Hofer, Stefanie
Gostner, Johanna M
Piater, Talia
Geisler, Simon
Weiss, Guenter
Loeffler-Ragg, Judith
Sonnweber, Thomas
Tancevski, Ivan
Pizzini, Alex
Sahanic, Sabina
Fuchs, Dietmar
Bellmann-Weiler, Rosa
Kurz, Katharina
author_facet Gietl, Mario
Burkert, Francesco
Seiwald, Stefanie
Böhm, Anna
Hofer, Stefanie
Gostner, Johanna M
Piater, Talia
Geisler, Simon
Weiss, Guenter
Loeffler-Ragg, Judith
Sonnweber, Thomas
Tancevski, Ivan
Pizzini, Alex
Sahanic, Sabina
Fuchs, Dietmar
Bellmann-Weiler, Rosa
Kurz, Katharina
author_sort Gietl, Mario
collection PubMed
description BACKGROUND: Fatigue, sleep disturbance, and neurological symptoms during and after COVID-19 are common and might be associated with inflammation-induced changes in tryptophan (Trp) and phenylalanine (Phe) metabolism. AIM: This pilot study investigated interferon gamma inducible biochemical pathways (namely Trp catabolism, neopterin, tyrosine [Tyr], and nitrite formation) during acute COVID-19 and reconvalescence. PATIENTS AND METHODS: Thirty one patients with moderate to severe COVID-19 admitted to the University Hospital of Innsbruck in early 2020 (March-May) were followed up. Neurotransmitter precursors Trp, Phe, Tyr as well as kynurenine (Kyn), neopterin, nitrite, and routine laboratory parameters were analyzed during acute infection and at a follow-up (FU) 60 days thereafter. Clinical symptoms of patients (neurological symptoms, fatigue, sleep disturbance) were recorded and associations with concentrations of laboratory parameters investigated. RESULTS AND CONCLUSION: Almost half of the patients suffered from neurological symptoms (48.4%), the majority of patients experienced sleep difficulties (56.7%) during acute COVID-19. Fatigue was present in nearly all patients. C-reactive protein (CRP), interleukin-6 (IL-6), neopterin, Kyn, Phe concentrations were significantly increased, and Trp levels depleted during acute COVID-19. Patients with sleep impairment and neurological symptoms during acute illness presented with increased CRP and IL-6 concentrations, Trp levels were lower in patients with sleep disturbance. In general, inflammatory markers declined during reconvalescence. A high percentage of patients suffered from persistent symptoms at FU (neurological symptoms: 17.2%, fatigue: 51.7%, sleeping disturbance: 34.5%) and had higher CRP concentrations. Nitrite and Phe levels were lower in patients with sleeping difficulties at FU and Kyn/Trp ratio, as indicator of IDO activity, was significantly lower in patients with neurological symptoms compared to patients without them at FU. In summary, inflammation induced alterations of amino acid metabolism might be related to acute and persisting symptoms of COVID-19.
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spelling pubmed-100769852023-04-06 Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19 Gietl, Mario Burkert, Francesco Seiwald, Stefanie Böhm, Anna Hofer, Stefanie Gostner, Johanna M Piater, Talia Geisler, Simon Weiss, Guenter Loeffler-Ragg, Judith Sonnweber, Thomas Tancevski, Ivan Pizzini, Alex Sahanic, Sabina Fuchs, Dietmar Bellmann-Weiler, Rosa Kurz, Katharina Int J Tryptophan Res Original Research BACKGROUND: Fatigue, sleep disturbance, and neurological symptoms during and after COVID-19 are common and might be associated with inflammation-induced changes in tryptophan (Trp) and phenylalanine (Phe) metabolism. AIM: This pilot study investigated interferon gamma inducible biochemical pathways (namely Trp catabolism, neopterin, tyrosine [Tyr], and nitrite formation) during acute COVID-19 and reconvalescence. PATIENTS AND METHODS: Thirty one patients with moderate to severe COVID-19 admitted to the University Hospital of Innsbruck in early 2020 (March-May) were followed up. Neurotransmitter precursors Trp, Phe, Tyr as well as kynurenine (Kyn), neopterin, nitrite, and routine laboratory parameters were analyzed during acute infection and at a follow-up (FU) 60 days thereafter. Clinical symptoms of patients (neurological symptoms, fatigue, sleep disturbance) were recorded and associations with concentrations of laboratory parameters investigated. RESULTS AND CONCLUSION: Almost half of the patients suffered from neurological symptoms (48.4%), the majority of patients experienced sleep difficulties (56.7%) during acute COVID-19. Fatigue was present in nearly all patients. C-reactive protein (CRP), interleukin-6 (IL-6), neopterin, Kyn, Phe concentrations were significantly increased, and Trp levels depleted during acute COVID-19. Patients with sleep impairment and neurological symptoms during acute illness presented with increased CRP and IL-6 concentrations, Trp levels were lower in patients with sleep disturbance. In general, inflammatory markers declined during reconvalescence. A high percentage of patients suffered from persistent symptoms at FU (neurological symptoms: 17.2%, fatigue: 51.7%, sleeping disturbance: 34.5%) and had higher CRP concentrations. Nitrite and Phe levels were lower in patients with sleeping difficulties at FU and Kyn/Trp ratio, as indicator of IDO activity, was significantly lower in patients with neurological symptoms compared to patients without them at FU. In summary, inflammation induced alterations of amino acid metabolism might be related to acute and persisting symptoms of COVID-19. SAGE Publications 2023-02-13 /pmc/articles/PMC10076985/ /pubmed/37038445 http://dx.doi.org/10.1177/11786469231154244 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Gietl, Mario
Burkert, Francesco
Seiwald, Stefanie
Böhm, Anna
Hofer, Stefanie
Gostner, Johanna M
Piater, Talia
Geisler, Simon
Weiss, Guenter
Loeffler-Ragg, Judith
Sonnweber, Thomas
Tancevski, Ivan
Pizzini, Alex
Sahanic, Sabina
Fuchs, Dietmar
Bellmann-Weiler, Rosa
Kurz, Katharina
Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19
title Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19
title_full Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19
title_fullStr Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19
title_full_unstemmed Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19
title_short Interferon-gamma Mediated Metabolic Pathways in Hospitalized Patients During Acute and Reconvalescent COVID-19
title_sort interferon-gamma mediated metabolic pathways in hospitalized patients during acute and reconvalescent covid-19
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076985/
https://www.ncbi.nlm.nih.gov/pubmed/37038445
http://dx.doi.org/10.1177/11786469231154244
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