Evidence map›Paper›PMID 30289974›Full record

ArticleJournal of neurochemistry2019

Reduced expression of the ferroptosis inhibitor glutathione peroxidase-4 in multiple sclerosis and experimental autoimmune encephalomyelitis.

Che-Lin Hu, Mara Nydes, Kara L Shanley, Itzy E Morales Pantoja, Tamara A Howard, Oscar A Bizzozero

Open access · greenAbstract read
In one paragraph

Article in Journal of neurochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

105 citing papers in PubMed, 205 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Cell death in multiple sclerosis.Cell death and differentiation · 2026
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Neuroferroptosis in health and diseases.Nature reviews. Neuroscience · 2025
    Review
  19. Article
  20. Review

45 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

6 authors at 1 institution in 1 country.

Che-Lin HuDepartment of Cell Biology and Physiology, University of New Mexico - Health Sciences Center, Albuquerque, New Mexico, USA.
Mara NydesDepartment of Cell Biology and Physiology, University of New Mexico - Health Sciences Center, Albuquerque, New Mexico, USA.
Kara L ShanleyDepartment of Cell Biology and Physiology, University of New Mexico - Health Sciences Center, Albuquerque, New Mexico, USA.
Itzy E Morales PantojaDepartment of Cell Biology and Physiology, University of New Mexico - Health Sciences Center, Albuquerque, New Mexico, USA.
Tamara A HowardDepartment of Cell Biology and Physiology, University of New Mexico - Health Sciences Center, Albuquerque, New Mexico, USA.
Oscar A BizzozeroDepartment of Cell Biology and Physiology, University of New Mexico - Health Sciences Center, Albuquerque, New Mexico, USA.ORCID 0000-0001-7597-3630
University of New Mexico · US

Funding

UNM Initiative to Maximize Student Diversity (IMSD)R25GM060201 · NIGMS · UNIVERSITY OF NEW MEXICO · PI WERNER-WASHBURNE, MARGRET C. · 2000 to 2017
$9.9M
The pathogenic role of protein aggregation in inflammatory demyelinationR21NS084042 · NINDS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BIZZOZERO, OSCAR A · 2013 to 2014
$413k
NIGMS NIH HHS R25 GM060201NINDS NIH HHS R21 NS084042
6 · The paper itself

Abstract

Glutathione peroxidase 4 (GPx4) is the only enzyme capable of reducing toxic lipid hydroperoxides in biological membranes to the corresponding alcohols using glutathione as the electron donor. GPx4 is the major inhibitor of ferroptosis, a non-apoptotic and iron-dependent programmed cell death pathway, which has been shown to occur in various neurological disorders with severe oxidative stress. In this study, we investigate whether GPx4 expression is altered in multiple sclerosis and its animal model experimental autoimmune encephalomyelitis (EAE). The results clearly show that mRNA expression for all three GPx4 isoforms (cytoplasmic, mitochondrial and nuclear) decline in multiple sclerosis gray matter and in the spinal cord of MOG

Indexed as

AdultAgedAged, 80 and overAnimalsBrainCell DeathEncephalomyelitis, Autoimmune, ExperimentalFemaleGlutathione PeroxidaseHumansIsoenzymesMaleMiceMice, Inbred C57BLMiddle AgedMitochondriaGlutathione PeroxidaseIsoenzymesPhospholipid Hydroperoxide Glutathione Peroxidaseexperimental autoimmune encephalomyelitisferroptosisglutathione peroxidase 4lipid peroxidationmitochondrial damagemultiple sclerosis

Identifiers

PMID30289974
PMCPMC6347488
OpenAlexW2894772721

What OpenQuestion holds

Textmetadata
LicenceTDM
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.