Evidence map›Paper›PMID 42548612›Full record

ReviewFrontiers in medicine2026

When barriers fail: the role of endothelial dysfunction in rare pediatric neuromuscular diseases.

Aleksandra Agafonova, Alessia Cosentino, Chiara Prinzi, Claudia Parano, Angela Trovato Salinaro, Maria Concetta Scuto, Giordana Riccioli, Gabriella Lupo, Carmelina Daniela Anfuso

Abstract readReview
In one paragraph

Review in Frontiers in medicine, 2026. 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

9 authors.

Aleksandra Agafonova *Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
Alessia Cosentino *Department of Biomedical and Biotechnological Sciences, University of Catania, Catania, Italy.
Chiara PrinziDepartment of Biomedical and Biotechnological Sciences, University of Catania, Catania, Italy.
Claudia ParanoDepartment of General Surgery and Medical-Surgical Specialties, University of Palermo, Palermo, Italy.
Angela Trovato SalinaroDepartment of Biomedical and Biotechnological Sciences, University of Catania, Catania, Italy.
Maria Concetta ScutoDepartment of Medicine and Surgery, Kore University of Enna, Enna, Italy.
Giordana RiccioliDepartment of General Surgery, University Hospital Policlinico G.Rodolico-San Marco, Catania, Italy.
Gabriella LupoDepartment of Biomedical and Biotechnological Sciences, University of Catania, Catania, Italy.
Carmelina Daniela AnfusoDepartment of Biomedical and Biotechnological Sciences, University of Catania, Catania, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rare pediatric neuromuscular diseases represent a heterogeneous group of disorders in which endothelial dysfunction and blood-tissue barrier alterations can contribute to disease onset and progression. The vascular endothelium, which lines blood vessels, plays a central role in regulating blood flow, immune cell trafficking, and maintaining the integrity of both the blood-brain barrier (BBB) and blood-nerve barrier (BNB). While BBB and the BNB share structural similarities, BNB endothelial cells are more restrictive due to a higher density of junctional complex proteins. Dysfunction of these barriers can lead to inadequate perfusion, neuroinflammation, and increased endothelial permeability. Evidence from rare conditions such as Duchenne muscular dystrophy (DMD), spinal muscular atrophy (SMA), Kawasaki Disease (KD), chronic inflammatory demyelinating polyneuropathy (CIDP), and acute inflammatory demyelinating polyradiculoneuropathy (AIDP) suggests that vascular and barrier abnormalities influence disease severity. However, the precise mechanisms underlying BNB disruption remain poorly understood for several disorders. Understanding these processes not only provides insights into disease pathophysiology but also highlights potential diagnostic and therapeutic targets. This review summarizes current knowledge on endothelial and barrier alterations in rare pediatric neuromuscular diseases, emphasizing the need for further studies to elucidate the involvement of BNB and guide future clinical interventions.

Indexed as

blood-brain barrierblood-nerve barrierDuchenne muscular dystrophyendothelial dysfunctioninflammatory demyelinating polyneuropathyKawasaki diseasepediatric neuromuscular diseasesspinal muscular atrophy

Identifiers

PMID42548612
PMCPMC13429647

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Registered trials

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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.