Evidence map›Paper›PMID 36743658›Full record

ArticleWorld journal of virology2023

COVID-19-related liver injury: Focus on genetic and drug-induced perspectives.

Deepak Parchwani, Amit D Sonagra, Sagar Dholariya, Anita Motiani, Ragini Singh

Open access · diamondAbstract read
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Article in World journal of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Deepak ParchwaniDepartment of Biochemistry, All India Institute of Medical Sciences, Rajkot 360001, India.
Amit D SonagraDepartment of Biochemistry, All India Institute of Medical Sciences, Rajkot 360001, India.
Sagar DholariyaDepartment of Biochemistry, All India Institute of Medical Sciences, Rajkot 360001, India. drsagar.dholariya@gmail.com.
Anita MotianiDepartment of Biochemistry, All India Institute of Medical Sciences, Rajkot 360001, India.
Ragini SinghDepartment of Biochemistry, All India Institute of Medical Sciences, Rajkot 360001, India.
All India Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEmpirical use of potentially hepatotoxic drugs in the management of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is considered as one of the major etiopathogenetic factors for liver injury. Recent evidence has shown that an underlying genetic factor may also occur. Hence, it is important to understand the host genetics and iatrogenic-based mechanisms for liver dysfunction to make timely remedial measures.

aimTo investigate drug-induced and genetic perspectives for the development of coronavirus disease 2019 (COVID-19)-related liver injury.

methodsReference Citation Analysis, PubMed, Google Scholar and China National Knowledge Infrastructure were searched by employing the relevant MeSH keywords and pertaining data of the duration, site and type of study, sample size with any subgroups and drug-induced liver injury outcome. Genetic aspects were extracted from the most current pertinent publications.

resultsIn all studies, the hepatic specific aminotransferase and other biochemical indices were more than their prescribed upper normal limit in COVID-19 patients and were found to be significantly related with the gravity of disease, hospital stay, number of COVID-19 treatment drugs and worse clinical outcomes. In addition, membrane bound O-acyltransferase domain containing 7 rs641738, rs11385942 G>GA at chromosome 3 gene cluster and rs657152 C>A at ABO blood locus was significantly associated with severity of livery injury in admitted SARS-CoV-2 patients.

conclusionHepatic dysfunction in SARS-CoV-2 infection could be the result of individual drugs or due to drug-drug interactions and may be in a subset of patients with a genetic propensity. Thus, serial estimation of hepatic indices in hospitalized SARS-CoV-2 patients should be done to make timely corrective actions for iatrogenic causes to avoid clinical deterioration. Additional molecular and translational research is warranted in this regard.

Indexed as

COVID-19Drug-induced liver injuryGenetic prospectiveLiver injuryPrognosisSARS-CoV-2

Identifiers

PMID36743658
PMCPMC9896591
OpenAlexW4317040273

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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.