Evidence map›Paper›PMID 35739983›Full record

ReviewAntioxidants (Basel, Switzerland)2022

Inherited Retinal Dystrophies: Role of Oxidative Stress and Inflammation in Their Physiopathology and Therapeutic Implications.

Isabel Pinilla, Victoria Maneu, Laura Campello, Laura Fernández-Sánchez, Natalia Martínez-Gil, Oksana Kutsyr, Xavier Sánchez-Sáez, Carla Sánchez-Castillo, Pedro Lax, Nicolás Cuenca

Open access · goldAbstract readReview
In one paragraph

Review in Antioxidants (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. A Structurally CharacterizedAntioxidants (Basel, Switzerland) · 2026
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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

10 authors at 2 institutions in 1 country.

Isabel PinillaAragón Health Research Institute (IIS Aragón), 50009 Zaragoza, Spain.ORCID 0000-0003-0349-9997
Victoria ManeuDepartment of Optics, Pharmacology and Anatomy, University of Alicante, 03690 Alicante, Spain.ORCID 0000-0002-5265-1361
Laura CampelloDepartment of Physiology, Genetics and Microbiology, University of Alicante, 03690 Alicante, Spain.ORCID 0000-0002-0869-1315
Laura Fernández-SánchezDepartment of Optics, Pharmacology and Anatomy, University of Alicante, 03690 Alicante, Spain.ORCID 0000-0002-3629-0156
Natalia Martínez-GilDepartment of Physiology, Genetics and Microbiology, University of Alicante, 03690 Alicante, Spain.ORCID 0000-0001-8882-5602
Oksana KutsyrDepartment of Physiology, Genetics and Microbiology, University of Alicante, 03690 Alicante, Spain.ORCID 0000-0002-1173-6916
Xavier Sánchez-SáezDepartment of Physiology, Genetics and Microbiology, University of Alicante, 03690 Alicante, Spain.
Carla Sánchez-CastilloDepartment of Physiology, Genetics and Microbiology, University of Alicante, 03690 Alicante, Spain.
Pedro LaxAlicante Institute for Health and Biomedical Research (ISABIAL), 03010 Alicante, Spain.ORCID 0000-0001-6931-1008
Nicolás CuencaAlicante Institute for Health and Biomedical Research (ISABIAL), 03010 Alicante, Spain.ORCID 0000-0002-6767-5710
University of Alicante · ESUniversidad de Zaragoza · ES

Funding

DGA and Fondo Europeo de Desarrollo Regional (FEDER) funds: "Una manera de hacer Europa". B08_17RGeneralitat Valenciana PROME- TEO/2021/024, IDIFEDER/2017/064Instituto de Salud Carlos III RETICS-FEDER-RD16/ 0008/0016Ministry of Science and Innovation cofinanced by European Regional Development Fund MICINN-FEDER PID2019-106230RB-I00
6 · The paper itself

Abstract

Inherited retinal dystrophies (IRDs) are a large group of genetically and clinically heterogeneous diseases characterized by the progressive degeneration of the retina, ultimately leading to loss of visual function. Oxidative stress and inflammation play fundamental roles in the physiopathology of these diseases. Photoreceptor cell death induces an inflammatory state in the retina. The activation of several molecular pathways triggers different cellular responses to injury, including the activation of microglia to eliminate debris and recruit inflammatory cells from circulation. Therapeutical options for IRDs are currently limited, although a small number of patients have been successfully treated by gene therapy. Many other therapeutic strategies are being pursued to mitigate the deleterious effects of IRDs associated with oxidative metabolism and/or inflammation, including inhibiting reactive oxygen species' accumulation and inflammatory responses, and blocking autophagy. Several compounds are being tested in clinical trials, generating great expectations for their implementation. The present review discusses the main death mechanisms that occur in IRDs and the latest therapies that are under investigation.

Indexed as

clinical trialinflammationinherited retinal dystrophiesoxidative stressreactive oxygen species

Identifiers

PMID35739983
PMCPMC9219848
OpenAlexW4281686363

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.