Evidence map›Paper›PMID 32632359›Full record

ArticleToxicology reports2020

Reactive oxygen species as an initiator of toxic innate immune responses in retort to SARS-CoV-2 in an ageing population, consider N-acetylcysteine as early therapeutic intervention.

Aikaterini Nasi, Stephanie McArdle, Gustav Gaudernack, Gabriel Westman, Cornelis Melief, Johan Rockberg, Ramon Arens, Demetrios Kouretas, Jan Sjölin, Sara Mangsbo

Open access · goldAbstract read
In one paragraph

Article in Toxicology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
2.2field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

62 citing papers in PubMed, 98 citations in OpenAlex.

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2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 5 countries.

Aikaterini NasiUltimovacs AB, Uppsala Sweden.
Stephanie McArdleStephanie McArdle, Nottingham Trenton University, The John van Geest Cancer Research Centre, Nottingham, UK.
Gustav GaudernackUltimovacs ASA, Oslo, Norway.
Gabriel WestmanDept Medical Sciences, Section of Infectious Diseases, Uppsala University, Uppsala, Sweden.
Cornelis MeliefLeiden University Medical Center, Leiden, the Netherlands.
Johan RockbergKungliga Tekniska Högskolan (KTH), Stockholm Sweden.
Ramon ArensLeiden University Medical Center, Leiden, the Netherlands.
Demetrios KouretasDept Biochemistry-Biotechnology, University of Thessaly, Larissa, Greece.
Jan SjölinDept Medical Sciences, Section of Infectious Diseases, Uppsala University, Uppsala, Sweden.
Sara MangsboUltimovacs AB, Uppsala Sweden.
Uppsala University · SELeiden University Medical Center · NLKTH Royal Institute of Technology · SENottingham Trent University · GBUltimovacs (Norway) · NOUniversity of Thessaly · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the current COVID-19 pandemic, a need for evaluation of already available drugs for treatment of the disease is crucial. Hereby, based on literature review from the current pandemic and previous outbreaks with corona viruses we analyze the impact of the virus infection on cell stress responses and redox balance. High levels of mortality are noticed in elderly individuals infected with SARS-CoV2 and during the previous SARS-CoV1 outbreak. Elderly individuals maintain a chronic low level of inflammation which is associated with oxidative stress and inflammatory cytokine production, a condition that increases the severity of viral infections in this population. Coronavirus infections can lead to alterations of redox balance in infected cells through modulation of NAD + biosynthesis, PARP function along with altering proteasome and mitochondrial function in the cell thereby leading to enhanced cell stress responses which further exacerbate inflammation. ROS production can increase IL-6 production and lipid peroxidation resulting in cell damage. Therefore, early treatment with anti-oxidants such as NAC during COVID-19 can be a way to bypass the excessive inflammation and cell damage that lead to severe infection, thus early NAC as intervention should be evaluated in a clinical trial setting.

Indexed as

AntioxidantsCOVID-19N-acetylcysteineOxidative stressSARS-CoV2

Identifiers

PMID32632359
PMCPMC7301821
OpenAlexW3036899921

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.