Evidence map›Paper›PMID 41006509›Full record

ArticleScientific reports2025

A two-site collaborative study of electrical impedance myography for evaluation of disease progression in murine Duchenne muscular dystrophy models.

Paola Mantuano, Maaike van Putten, Buket Sonbas Cobb, Kayleigh Putker, Brigida Boccanegra, Christa Tanganyika-de Winter, Lisamaura Tulimiero, Anne-Fleur Schneider, Ornella Cappellari, Davy Van De Vijver and 4 more

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Paola Mantuano *Department of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", Bari, Italy.
Maaike van Putten *Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Buket Sonbas CobbDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, USA.
Kayleigh PutkerDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Brigida BoccanegraDepartment of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", Bari, Italy.
Christa Tanganyika-de WinterDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Lisamaura TulimieroDepartment of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", Bari, Italy.
Anne-Fleur SchneiderDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Ornella CappellariDepartment of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", Bari, Italy.
Davy Van De VijverDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Sarah EngelbeenDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Sarbesh PandeyaDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, USA.
Janice A NagyDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, USA.
Seward RutkoveDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, USA. srutkove@bidmc.harvard.edu.

Funding

Charlies Fund naDuchenne UK naTUBITAK 2219-International Postdoctoral Research Fellowship Program for Turkish Citizens
6 · The paper itself

Abstract

Accessibility to outcome measures that reliably assess disease pathology in preclinical studies are vital, especially for rare disorders such as Duchenne muscular dystrophy (DMD). The non-invasive technique of electrical impedance myography (EIM) has shown potential as an outcome measure in patients and mouse models of neuromuscular disorders. However, these preclinical observations have been limited to a single site. Here, we performed a longitudinal, parallel two-site study to assess the potential of EIM as an outcome measure by using two DMD mouse models - mdx mice on a C57BL/10ScSn/J or DBA/2J genetic background - differing in disease severity, and being hypertrophic and atrophic, respectively, over a ten-month period, in which mice were evaluated monthly. We found that longitudinally acquired phase values were the most reliable, with relatively minor differences between study sites. Histopathology, assessed at 8, 12, 28, or 52 weeks of age correlated well with EIM phase values in both models. Our findings highlight the applicability of EIM as a robust, preclinical outcome measure for DMD.

Indexed as

Electric ImpedanceMuscular Dystrophy, DuchenneMyographyAnimalsDisease Models, AnimalDisease ProgressionMaleMiceMice, Inbred C57BLMice, Inbred DBAMice, Inbred mdxMuscle, SkeletalDuchenne muscular dystrophyElectrical impedance myographyHistopathologyMouse modelNatural history study

Identifiers

PMID41006509
PMCPMC12475182

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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.