Hiding in Plain Sight: an Approach to Treating Patients with Severe COVID-19 Infection.
Identifieur interne : 001409 ( Ncbi/Checkpoint ); précédent : 001408; suivant : 001410Hiding in Plain Sight: an Approach to Treating Patients with Severe COVID-19 Infection.
Auteurs : David S. Fedson [Oman] ; Steven M. Opal [États-Unis] ; Ole Martin Rordam [Norvège]Source :
- mBio [ 2150-7511 ] ; 2020.
Descripteurs français
- KwdFr :
- Antagonistes du récepteur de type 2 de l'angiotensine-II (usage thérapeutique), Humains, Infections à coronavirus (), Infections à coronavirus (métabolisme), Infections à coronavirus (virologie), Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase (usage thérapeutique), Peptidyl-Dipeptidase A (métabolisme), Pneumopathie virale (), Pneumopathie virale (métabolisme), Pneumopathie virale (virologie), Récepteur de type 2 à l'angiotensine-II (biosynthèse), Récepteurs viraux (biosynthèse).
- MESH :
- biosynthèse : Récepteur de type 2 à l'angiotensine-II, Récepteurs viraux.
- métabolisme : Infections à coronavirus, Peptidyl-Dipeptidase A, Pneumopathie virale.
- usage thérapeutique : Antagonistes du récepteur de type 2 de l'angiotensine-II, Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase.
- virologie : Infections à coronavirus, Pneumopathie virale.
- Humains, Infections à coronavirus, Pneumopathie virale.
English descriptors
- KwdEn :
- Angiotensin II Type 2 Receptor Blockers (therapeutic use), Betacoronavirus, Coronavirus Infections (metabolism), Coronavirus Infections (therapy), Coronavirus Infections (virology), Humans, Hydroxymethylglutaryl-CoA Reductase Inhibitors (therapeutic use), Peptidyl-Dipeptidase A (metabolism), Pneumonia, Viral (metabolism), Pneumonia, Viral (therapy), Pneumonia, Viral (virology), Receptor, Angiotensin, Type 2 (biosynthesis), Receptors, Virus (biosynthesis).
- MESH :
- chemical , biosynthesis : Receptor, Angiotensin, Type 2, Receptors, Virus.
- chemical , metabolism : Peptidyl-Dipeptidase A.
- chemical , therapeutic use : Angiotensin II Type 2 Receptor Blockers, Hydroxymethylglutaryl-CoA Reductase Inhibitors.
- metabolism : Coronavirus Infections, Pneumonia, Viral.
- therapy : Coronavirus Infections, Pneumonia, Viral.
- virology : Coronavirus Infections, Pneumonia, Viral.
- Betacoronavirus, Humans.
Abstract
Patients with COVID-19 infection are at risk of acute respiratory disease syndrome (ARDS) and death. The tissue receptor for COVID-19 is ACE2, and higher levels of ACE2 can protect against ARDS. Angiotensin receptor blockers and statins upregulate ACE2. Clinical trials are needed to determine whether this drug combination might be used to treat patients with severe COVID-19 infection.
DOI: 10.1128/mBio.00398-20
PubMed: 32198163
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000195
- to stream PubMed, to step Curation: 000195
- to stream PubMed, to step Checkpoint: 000656
- to stream Ncbi, to step Merge: 001409
- to stream Ncbi, to step Curation: 001409
Links to Exploration step
pubmed:32198163Le document en format XML
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<term>Coronavirus Infections (therapy)</term>
<term>Coronavirus Infections (virology)</term>
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<term>Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase (usage thérapeutique)</term>
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<front><div type="abstract" xml:lang="en">Patients with COVID-19 infection are at risk of acute respiratory disease syndrome (ARDS) and death. The tissue receptor for COVID-19 is ACE2, and higher levels of ACE2 can protect against ARDS. Angiotensin receptor blockers and statins upregulate ACE2. Clinical trials are needed to determine whether this drug combination might be used to treat patients with severe COVID-19 infection.</div>
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<li>États-Unis</li>
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