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About:
COVID-19 infection results in alterations of the kynurenine pathway and fatty acid metabolism that correlate with IL-6 levels and renal status
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wasabi.inria.fr
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Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
COVID-19 infection results in alterations of the kynurenine pathway and fatty acid metabolism that correlate with IL-6 levels and renal status
Creator
Alessandro, Angelo
D'alessandro, Angelo
Francis, Richard
Hansen, Kirk
Hod, Eldad
Hudson, Krystalyn
Spitalnik, Steven
Thomas, Tiffany
Zimring, James
Bertolone, Lorenzo
Nemkov, Travis
Reisz, Julie
Stefanoni, Davide
source
MedRxiv; Medline
abstract
Previous studies suggest a role for systemic reprogramming of host metabolism during viral pathogenesis to fuel rapidly expanding viral proliferation, for example by providing free amino acids and fatty acids as building blocks. In addition, general alterations in metabolism can provide key understanding of pathogenesis. However, little is known about the specific metabolic effects of SARS-COV-2 infection. The present study evaluated the serum metabolism of COVID-19 patients (n=33), identified by a positive nucleic acid test of a nasopharyngeal swab, as compared to COVID-19-negative control patients (n=16). Targeted and untargeted metabolomics analyses specifically identified alterations in the metabolism of tryptophan into the kynurenine pathway, which is well-known to be involved in regulating inflammation and immunity. Indeed, the observed changes in tryptophan metabolism correlated with serum interleukin-6 (IL-6) levels. Metabolomics analysis also confirmed widespread dysregulation of nitrogen metabolism in infected patients, with decreased circulating levels of most amino acids, except for tryptophan metabolites in the kynurenine pathway, and increased markers of oxidant stress (e.g., methionine sulfoxide, cystine), proteolysis, and kidney dysfunction (e.g., creatine, creatinine, polyamines). Increased circulating levels of glucose and free fatty acids were also observed, consistent with altered carbon homeostasis in COVID-19 patients. Metabolite levels in these pathways correlated with clinical laboratory markers of inflammation and disease severity (i.e., IL-6 and C-reactive protein) and renal function (i.e., blood urea nitrogen). In conclusion, this initial observational study of the metabolic consequences of COVID-19 infection in a clinical cohort identified amino acid metabolism (especially kynurenine and cysteine/taurine) and fatty acid metabolism as correlates of COVID-19, providing mechanistic insights, potential markers of clinical severity, and potential therapeutic targets.
has issue date
2020-05-16
(
xsd:dateTime
)
bibo:doi
10.1101/2020.05.14.20102491
bibo:pmid
32511571
has license
medrxiv
sha1sum (hex)
3b3c11a8d7b5b401e9fba6411a356eb22f9ba565
schema:url
https://doi.org/10.1101/2020.05.14.20102491
resource representing a document's title
COVID-19 infection results in alterations of the kynurenine pathway and fatty acid metabolism that correlate with IL-6 levels and renal status
has PubMed identifier
32511571
schema:publication
medRxiv : the preprint server for health sciences
resource representing a document's body
covid:3b3c11a8d7b5b401e9fba6411a356eb22f9ba565#body_text
is
schema:about
of
named entity 'metabolomics'
named entity 'host'
named entity 'tryptophan metabolism'
named entity 'negative control'
named entity 'provide'
named entity 'proliferation'
named entity 'circulating'
named entity 'observed'
named entity 'serum'
named entity 'proteolysis'
named entity 'authors'
named entity 'CONSISTENT WITH'
named entity 'PATIENTS'
named entity 'PROTEOLYSIS'
named entity 'HOST'
named entity 'POSITIVE'
named entity 'PROVIDE'
named entity 'NITROGEN METABOLISM'
named entity 'SUGGEST'
named entity 'CYSTINE'
named entity 'CREATININE'
named entity 'METABOLOMICS'
named entity 'VIRAL PROLIFERATION'
named entity 'GENERAL'
named entity 'PROVIDING'
named entity 'POLYAMINES'
named entity 'ALTERATIONS'
named entity 'NASOPHARYNGEAL SWAB'
named entity 'SYSTEMIC'
covid:arg/3b3c11a8d7b5b401e9fba6411a356eb22f9ba565
named entity 'dysfunction'
named entity 'involved'
named entity 'metabolism'
named entity 'metabolism'
named entity 'critically ill patients'
named entity 'serum'
named entity 'sulfur metabolism'
named entity 'CLIA'
named entity 'metabolome'
named entity 'viral load'
named entity 'pentose'
named entity 'Declaration of Helsinki'
named entity 'Wuhan'
named entity 'sera'
named entity 'nicotinic acid'
named entity 'long-chain'
named entity 'serological testing'
named entity 'fatty acid desaturase'
named entity 'levels'
named entity 'study'
named entity 'IL-6'
named entity 'metabolomics'
named entity 'metabolic effects'
named entity 'amino acids'
named entity 'nucleic acid test'
named entity 'metabolism of tryptophan'
named entity 'infection'
named entity 'tryptophan'
named entity 'viral pathogenesis'
named entity 'kidney dysfunction'
named entity 'nitrogen metabolism'
named entity 'proteolysis'
named entity 'fatty acid metabolism'
named entity 'preprint'
named entity 'hypercoagulability'
named entity 'upper respiratory tract'
named entity 'COVID'
named entity 'platelet'
named entity 'serum'
named entity 'antimalarial drugs'
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