Evidence map›Paper›PMID 36790443›Full record

ReviewPsychopharmacology2023

Pathophysiological basis and promise of experimental therapies for Gulf War Illness, a chronic neuropsychiatric syndrome in veterans.

Maheedhar Kodali, Tanvi Jankay, Ashok K Shetty, Doodipala Samba Reddy

Abstract readReview
PubMed Publisher
In one paragraph

Review in Psychopharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. FDA-approved cannabidiol [EpidiolexMilitary Medical Research · 2024
    Article
  6. Review
  7. Article
  8. Review
  9. Nicotinamide Riboside, a Promising Vitamin BMolecules (Basel, Switzerland) · 2023
    Review
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

4 authors at 3 institutions in 1 country.

Maheedhar KodaliInstitute for Regenerative Medicine, Department of Molecular and Cellular Medicine, Texas A&M University School of Medicine, College Station, TX, USA.
Tanvi JankayDepartment of Neuroscience and Experimental Therapeutics, Texas A&M University School of Medicine, Bryan, TX, USA.
Ashok K ShettyInstitute for Regenerative Medicine, Department of Molecular and Cellular Medicine, Texas A&M University School of Medicine, College Station, TX, USA.
Doodipala Samba ReddyDepartment of Neuroscience and Experimental Therapeutics, Texas A&M University School of Medicine, Bryan, TX, USA. sambareddy@tamu.edu.ORCID http://orcid.org/0000-0003-2735-9550
Texas A&M Health Science Center · USTexas A&M Health Science Center · USTexas A&M University · US

Funding

DOD Peer Reviewed Cancer Research Program W81XWH-19-1-0702DOD Peer Reviewed Cancer Research Program W81XWH-21-1-0305DOD Peer Reviewed Cancer Research Program W81XWH-21-1-0311DOD Peer Reviewed Cancer Research Program W81XWH-21-1-0314
6 · The paper itself

Abstract

This article describes the pathophysiology and potential treatments for Gulf War Illness (GWI), which is a chronic neuropsychiatric illness linked to a combination of chemical exposures experienced by service personnel during the first Gulf War in 1991. However, there is currently no effective treatment for veterans with GWI. The article focuses on the current status and efficacy of existing therapeutic interventions in preclinical models of GWI, as well as potential perspectives of promising therapies. GWI stems from changes in brain and peripheral systems in veterans, leading to neurocognitive deficits, as well as physiological and psychological effects resulting from multifaceted changes such as neuroinflammation, oxidative stress, and neuronal damage. Aging not only renders veterans more susceptible to GWI symptoms, but also attenuates their immune capabilities and response to therapies. A variety of experimental models are being used to investigate the pathophysiology and develop therapies that have the ability to alleviate devastating symptoms. Over two dozen therapeutic interventions targeting neuroinflammation, mitochondrial dysfunction, neuronal injury, and neurogenesis are being tested, including agents such as curcumin, curcumin nanoparticles, monosodium luminol, melatonin, resveratrol, fluoxetine, rolipram, oleoylethanolamide, ketamine, levetiracetam, nicotinamide riboside, minocycline, pyridazine derivatives, and neurosteroids. Preclinical outcomes show that some agents have promise, including curcumin, resveratrol, and ketamine, which are being tested in clinical trials in GWI veterans. Neuroprotectants and other compounds such as monosodium luminol, melatonin, levetiracetam, oleoylethanolamide, and nicotinamide riboside appear promising for future clinical trials. Neurosteroids have been shown to have neuroprotective and disease-modifying properties, which makes them a promising medicine for GWI. Therefore, accelerated clinical studies are urgently needed to evaluate and launch an effective therapy for veterans displaying GWI.

Indexed as

CurcuminKetamineMelatoninNeurosteroidsPersian Gulf SyndromeVeteransGulf WarHumansLevetiracetamLuminolNeuroinflammatory DiseasesResveratrolTherapies, InvestigationalCurcuminKetamineLevetiracetamLuminolMelatoninNeurosteroidsResveratrolBiomarkersChemical exposureGulf War IllnessOrganophosphatesSymptomsVeterans

Identifiers

PMID36790443
OpenAlexW4320857351

What OpenQuestion holds

Textmetadata
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.