Evidence map›Paper›PMID 40489651›Full record

ReviewRevista medica del Instituto Mexicano del Seguro Social2025

[Benefits of ω-3 fatty acids in Duchenne muscular dystrophy].

José Emilio Galeazzi-Aguilar, Maricela Rodríguez-Cruz

Abstract readReviewEnglish Abstract
In one paragraph

Review in Revista medica del Instituto Mexicano del Seguro Social, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

José Emilio Galeazzi-AguilarUniversidad Nacional Autónoma de México, Facultad de Medicina, Posgrado en Ciencias Biomédicas. Ciudad de México, México.ORCID 0009-0002-6664-4178
Maricela Rodríguez-CruzInstituto Mexicano del Seguro Social, Centro Médico Nacional Siglo XXI, Hospital de Pediatría "Dr. Silvester Frenk Freund", Unidad de Investigación Médica en Nutrición. Ciudad de México, México.ORCID 0000-0001-8496-4023

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duchenne Muscular Dystrophy (DMD), caused by mutations in the dystrophin gene, is the most common congenital muscular dystrophy and is characterized by a chronic inflammatory response mediated by immune cells and cytokines. Obesity, a common feature of DMD, exacerbates this inflammation. Although corticosteroids are the conventional treatment, their adverse effects are substantial. The use of omega-3 polyunsaturated fatty acids (PUFAω-3) as adjuvant therapy is under investigation. A comprehensive review of studies from 2011 to May 2024 reveals that supplementation with PUFAω-3 has beneficial effects in mdx mice, a model of DMD. These include reduction of the inflammatory process in both muscle and circulation, in addition to decreased myonecrosis, resulting in improved muscle strength and endurance. Supplementation also had a positive impact on cardiac tissue, reducing fibrosis and inflammation present in this tissue. These results were corroborated in patients with DMD. A significant decrease in inflammatory markers such as NF-kB, IL-1β and IL-6 was observed with PUFAω-3, and an increase in the anti-inflammatory cytokine IL-10, suggesting a potential anti-inflammatory effect. These findings support the use of PUFAω-3 as adjuvant therapy in DMD, although further research is needed to fully understand its mechanisms and clinical benefits.

Indexed as

Dietary SupplementsFatty Acids, Omega-3Muscular Dystrophy, DuchenneAnimalsHumansMiceMice, Inbred mdxFatty Acids, Omega-3Body CompositionFatty Acids, Omega-3InflammationInsulin ResistanceMuscular Dystrophy, Duchenne

Identifiers

PMID40489651
PMCPMC12162134

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.