Evidence map›Paper›PMID 40325330›Full record

ArticleMolecular neurobiology2025

Exploratory Analysis of Gut Microbiota Profile in Duchenne Muscular Dystrophy (DMD) Patients with Intellectual Disability.

Chiara Panicucci, Sara Casalini, Giovanni Fiorito, Alessandra Biolcati Rinaldi, Valentina Biagioli, Davide Cangelosi, Noemi Brolatti, Elisa Principi, Serena Baratto, Marina Pedemonte and 6 more

Abstract read
In one paragraph

Article in Molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Trial
  2. Review
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

16 authors.

Chiara PanicucciCentre of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Sara CasaliniCentre of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Giovanni FioritoClinical Bioinformatics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Alessandra Biolcati RinaldiClinical Psychology Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Valentina BiagioliPediatric Neurology and Muscle Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Davide CangelosiClinical Bioinformatics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Noemi BrolattiCentre of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Elisa PrincipiCentre of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Serena BarattoCentre of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Marina PedemontePediatric Neurology and Muscle Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Simone MorandoCentre of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Antonella RivaPediatric Neurology and Muscle Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Cristina VenturinoClinical Psychology Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Pasquale StrianoPediatric Neurology and Muscle Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Paolo UvaClinical Bioinformatics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Claudio BrunoCentre of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy. claudiobruno@gaslini.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigates the differences in gut microbiota composition between DMD patients with (DMD +) and without (DMD -) intellectual disability (ID) and its potential role in cognitive outcomes. In this study, we assessed the gut microbiota in 50 genetically confirmed DMD patients (median age 13.1 years) using 16S rRNA gene sequencing. Cognitive assessment was performed using the Wechsler Intelligence Scales, with ID defined as an IQ < 70. Stool samples were analyzed, and statistical methods were used to assess alpha- and beta-diversity. Thirty-four percent of patients had ID. No significant differences were found in alpha-diversity or in the Firmicutes/Bacteroidetes ratio. However, beta-diversity analysis revealed significant differences between DMD + and DMD - groups, including, in DMD + , an increased abundance of Propionibacterium and Bifidobacterium, and a reduction in Bulleidia. These bacteria are involved in metabolic pathways that can influence neurological health through the gut-brain axis, particularly via the production of short-chain fatty acids. While these preliminary findings suggest a possible association between gut microbiota profile and cognitive impairment in DMD, further research is needed to explore a causal relationship and consider microbiota-targeted therapeutic strategies.

Indexed as

Gastrointestinal MicrobiomeIntellectual DisabilityMuscular Dystrophy, DuchenneAdolescentBacteriaChildFemaleHumansMaleRNA, Ribosomal, 16SRNA, Ribosomal, 16S16S rRNA gene sequencingDuchenne muscular dystrophyGut-brain axisIntellectual disabilityMetagenomics

Identifiers

PMID40325330
PMCPMC12367937

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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.