Evidence map›Paper›PMID 38090544›Full record

ReviewActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2023

Cognitive function in DMD carriers: personal case series and literature review.

Laura Carraro, Arianna Iosca, Maria Irene Dainesi, Sara Fusco, Daniela Pia Rosaria Chieffo, Federica Moriconi, Giulia d'Amario, Marika Pane, Eugenio Mercuri, Angela Berardinelli

Open access · greenAbstract readReview
In one paragraph

Review in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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 3 institutions in 2 countries.

Laura CarraroDepartment of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy.
Arianna IoscaDepartment of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy.
Maria Irene DainesiDepartment of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy.
Sara FuscoDepartment of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy.
Daniela Pia Rosaria ChieffoClinical Psychology Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Federica MoriconiClinical Psychology Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Giulia d'AmarioDepartment of Life Science and Public Health, Pediatric Neurology, Catholic University of Sacred Heart, Rome, Italy.
Marika PaneDepartment of Life Science and Public Health, Pediatric Neurology, Catholic University of Sacred Heart, Rome, Italy.
Eugenio MercuriDepartment of Life Science and Public Health, Pediatric Neurology, Catholic University of Sacred Heart, Rome, Italy.
Angela BerardinelliCasimiro Mondino Foundation, IRCCS, Pavia, Italy.
University of Pavia · ITUniversity of the Sacred Heart · JPAgostino Gemelli University Polyclinic · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Improvement in clinical conditions allowed physicians to pay more attention to the cognitive function in DMD patients, leading to description of a cognitive impairment not only in affected males, but in female carriers as well. This study aimed to investigate the cognitive involvement in a cohort of DMD carriers and to summarize the current knowledge about the intellectual involvement and neuropsychological profile in DMD/BMD carriers. Our case series consisted of 22 carrier patients from two different centers (IRCCS Mondino, Pavia and Policlinico Gemelli, Rome), for whom we retrospectively collected cognitive, clinical and genetic data. For literature review, we selected 9 studies published in English language from 2011 to 2023 and cited in PubMed. We found that the average IQ of DMD carriers was lower (74; very low) than the average score on normal curve (100 as average standard score). Furthermore, about 50% of them fell in the "extremely low IQ" range, compared with 2-3% of general population. A higher incidence of intellectual disability was confirmed in symptomatic DMD carriers (mean IQ 66; extremely low) from IRCCS Mondino, but not in the asymptomatic ones (mean IQ 99; average), when compared to the general population. Current literature, albeit limited, seems to confirm the presence of a cognitive impairment in carriers, although milder than in affected males but with a similar neuropsychological profile. However, further studies are necessary to delve deeper into this issue and provide adequate educational support.

Indexed as

Cognitive DysfunctionMuscular Dystrophy, DuchenneCognitionDystrophinFemaleHumansMaleMuscle, SkeletalRetrospective StudiesDystrophincarrierscognitionDMDDp140Duchenneisoform

Identifiers

PMID38090544
PMCPMC10712655
OpenAlexW4389802805

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.