Evidence map›Paper›PMID 39093886›Full record

ArticlePloS one2024

Valproic acid use is associated with diminished risk of contracting COVID-19, and diminished disease severity: Epidemiologic and in vitro analysis reveal mechanistic insights.

Amanda Watson, Pankil Shah, Doug Lee, Sitai Liang, Geeta Joshi, Ediri Metitiri, Wasim H Chowdhury, Dean Bacich, Peter Dube, Yan Xiang and 3 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Article
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

13 authors.

Amanda WatsonGlenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.ORCID 0000-0001-6893-1926
Pankil ShahDepartment of Urology, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.
Doug LeeDepartment of Urology, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.
Sitai LiangDepartment of Urology, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.
Geeta JoshiDepartment of Urology, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.ORCID 0000-0002-1396-0153
Ediri MetitiriDepartment of Urology, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.ORCID 0000-0001-7724-7288
Wasim H ChowdhuryDepartment of Urology, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.ORCID 0000-0002-6731-646X
Dean BacichDepartment of Urology, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.
Peter DubeBoehringer Ingelheim in Ames, Ames, Iowa, United States of America.
Yan XiangDepartment of Microbiology, Immunology and Molecular Genetics, University of Texas Health Science Center San Antonio San Antonio, Texas, United States of America.
Daniel HanleyDepartment of Neurology & Neurosurgery, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.
Luis Martinez-SobridoTexas Biomedical Research Institute, San Antonio, Texas, United States of America.
Ronald RodriguezDepartment of Medical Education, and Department of Urology, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.ORCID 0000-0001-7592-1435

Funding

Johns Hopkins-Tufts Trial Innovation Center HEAL Pain ERN SupplementU24TR001609 · NCATS · JOHNS HOPKINS UNIVERSITY · PI HANLEY, DANIEL F · 2016 to 2022
$36.3M
Johns Hopkins University Trial Innovation CenterU24TR004440 · NCATS · JOHNS HOPKINS UNIVERSITY · PI DANIEL F HANLEY · 2023 to 2026
$19.6M
CTSA K12 Program at The University of Texas Health Science Center at San AntonioK12TR004529 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ALISON G CAHILL, JOEL TSEVAT · 2023 to 2026
$4.1M
NCATS NIH HHS K12 TR004529NCATS NIH HHS U24 TR001609NCATS NIH HHS U24 TR004440
6 · The paper itself

Abstract

The SARS-CoV-2 pandemic has caused unprecedented worldwide infections from persistent mutant variants with various degrees of infectivity and virulence. The elusiveness of a highly penetrant, worldwide vaccination strategy suggests that the complete eradication of SARS-CoV-2 is unlikely. Even with the advent of new antiviral agents, the disease burden worldwide continues to exceed current preventative and therapeutic strategies. Greater interest has been placed towards the development of affordable,broadly effective antiviral therapeutics. Here, we report that the small branched-chain fatty acid Valproic acid (VPA), approved for maintenance of seizure and bipolar disorder, has a novel anti- coronavirus activity that can be augmented with the addition of a long-chain, polyunsaturated omega-3 fatty acid, Docosahexaenoic acid (DHA). An EMR-based epidemiological study of patients tested for COVID-19 demonstrated a correlation exists between a reduced infection rate in patients treated withVPA of up to 25%, as well as a decreased risk of emergency room visits, hospitalization, ICU admission,and use of mechanical ventilation. In vitro studies have demonstrated that VPA modifies gene expression in MRC5 cells. Interestingly, VPA correlates with the inhibition of several SARS-CoV2 interacting genes and the greater inhibition of alpha-coronavirus HCoV-229E (a "common cold" virus) and SARS-CoV2. The VPA-DHA combination activates pre-existing intracellular antiviral mechanisms normally repressed by coronaviruses. Gene expression profiles demonstrate subtle differences in overall gene expression between VPA-treated and VPA-DHA-treated cells. HCoV-229E infection caused an intensely different response with a marked induction of multiple intracellular inflammatory genes. Changes in gene expression took at least 24 hours to manifest and most likely why prior drug screens failed to identify any antiviral VPA activity despite in silico predictions. This report demonstrates an interaction between HDAC inhibition and the potent activation of cellular antiviral responses. A foundation now exists for a low-cost, highly effective antiviral strategy when supplemented with DHA.

Indexed as

Antiviral AgentsCOVID-19SARS-CoV-2Valproic AcidCOVID-19 Drug TreatmentDocosahexaenoic AcidsFemaleHumansMaleMiddle AgedSeverity of Illness IndexAntiviral AgentsDocosahexaenoic AcidsValproic Acid

Identifiers

PMID39093886
PMCPMC11296636

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.