ReviewFrontiers in medicine2026
When barriers fail: the role of endothelial dysfunction in rare pediatric neuromuscular diseases.
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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
What OpenQuestion holds
Registered trials
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.