Evidence map›Paper›PMID 40305278›Full record

ReviewBiomolecules2025

Oxidative Stress in Huntington's Disease.

Félix Javier Jiménez-Jiménez, Hortensia Alonso-Navarro, Elena García-Martín, Alba Cárcamo-Fonfría, María Del Mar Caballero-Muñoz, José A G Agúndez

Abstract readReview
In one paragraph

Review in Biomolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Fidelity of DNA ligase I is sensitive to physiological MgThe Journal of biological chemistry · 2026
    Article
  4. Huntington's disease LIG1 modifier variant increases ligase fidelity and suppresses somatic CAG repeat expansion.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Review
  6. Review
  7. Review
  8. 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

6 authors.

Félix Javier Jiménez-JiménezSection of Neurology, Hospital Universitario del Sureste, Arganda del Rey, 28500 Madrid, Spain.ORCID 0000-0002-7558-7323
Hortensia Alonso-NavarroSection of Neurology, Hospital Universitario del Sureste, Arganda del Rey, 28500 Madrid, Spain.ORCID 0000-0001-8644-2210
Elena García-MartínUniversity Institute of Molecular Pathology Biomarkers, Universidad de Extremadura, 10071 Cáceres, Spain.ORCID 0000-0002-8094-046X
Alba Cárcamo-FonfríaSection of Neurology, Hospital Universitario del Sureste, Arganda del Rey, 28500 Madrid, Spain.ORCID 0000-0002-9928-6293
María Del Mar Caballero-MuñozSection of Neurology, Hospital Universitario del Sureste, Arganda del Rey, 28500 Madrid, Spain.
José A G AgúndezUniversity Institute of Molecular Pathology Biomarkers, Universidad de Extremadura, 10071 Cáceres, Spain.ORCID 0000-0001-6895-9160

Funding

Fondo de Investigación Sanitaria, Instituto de Salud Carlos III, Madrid, Spain PI21/01683Fondo de Investigación Sanitaria, Instituto de Salud Carlos III, Madrid, Spain PI24/01358
6 · The paper itself

Abstract

Although the pathogenesis of the neurodegenerative phenomena of Huntington's disease (HD) is not well known, in the last 30 years, numerous data have been published that suggest a possible role of oxidative stress. The majority of studies regarding this issue were performed in different experimental models of this disease (neurotoxic models such as intraperitoneal injection of 3-nitropropionic acid or intrastriatal injection of quinolinic acid, transgenic animal models for HD, and cell cultures) and, less frequently, in samples of brain tissue, plasma/serum, blood cells, and other tissues from patients with a genetic-molecular diagnosis of presymptomatic and symptomatic HD compared to healthy controls. In this narrative review, we have summarized the data from the main studies in which oxidative stress parameters have been measured both in patients with HD and in experimental models of the same disease, as well as the few studies on gene variants involved in oxidative stress in patients with HD. Most studies addressing this issue in experimental models of HD have shown an increase in markers or oxidative stress, a decrease in antioxidant substances, or both. However, the results of studies on patients with HD have not been conclusive as few studies have been published on the matter. However, a meta-analysis of blood studies on HD patients (including a pool of serum and blood cell studies) has shown an increase in lipid peroxidation markers, OH8dG concentrations, and GPx activity and a decrease in GSH levels. Future prospective and multicenter studies with a long-term follow-up period involving a large number of HD patients and healthy controls are needed to address this topic.

Indexed as

Huntington DiseaseOxidative StressAnimalsBiomarkersDisease Models, AnimalHumansBiomarkersanimal modelsbiological markersHuntington’s diseaseoxidative stresspathogenesis

Identifiers

PMID40305278
PMCPMC12025275

What OpenQuestion 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 OpenQuestion graph.