Evidence map›Paper›PMID 35642830›Full record

ArticleDisease models & mechanisms2022

Natural history study and statistical modeling of disease progression in a preclinical model of myotubular myopathy.

Suzie Buono, Arnaud Monseur, Alexia Menuet, Anne Robé, Catherine Koch, Jocelyn Laporte, Leen Thielemans, Marion Depla, Belinda S Cowling

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Article in Disease models & mechanisms, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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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

5 citing papers in PubMed.

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4 · The record

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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.

Suzie BuonoDynacure, Illkirch 67400, France.ORCID 0000-0001-5694-2249
Arnaud MonseurPharmalex, Mont-St-Guibert 1435, Belgium.
Alexia MenuetDynacure, Illkirch 67400, France.
Anne RobéDynacure, Illkirch 67400, France.
Catherine KochDynacure, Illkirch 67400, France.
Jocelyn LaporteInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Institut National de la Santé et de la Recherche Médicale U1258, Centre National de la Recherche Scientifique UMR7104, Université de Strasbourg, 67404 Illkirch, France.ORCID 0000-0001-8256-5862
Leen ThielemansDynacure, Illkirch 67400, France.
Marion DeplaDynacure, Illkirch 67400, France.ORCID 0000-0003-4651-9302
Belinda S CowlingDynacure, Illkirch 67400, France.ORCID 0000-0001-6915-2596

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Generating reliable preclinical data in animal models of disease is essential in therapy development. Here, we performed statistical analysis and joint longitudinal-survival modeling of the progressive phenotype observed in Mtm1-/y mice, a reliable model for myotubular myopathy. Analysis of historical data was used to generate a model for phenotype progression, which was then confirmed with phenotypic data from a new colony of mice derived via in vitro fertilization in an independent animal house, highlighting the reproducibility of disease phenotype in Mtm1-/y mice. These combined data were used to refine the phenotypic parameters analyzed in these mice and improve the model generated for expected disease progression. The disease progression model was then used to test the therapeutic efficacy of Dnm2 targeting. Dnm2 reduction by antisense oligonucleotides blocked or postponed disease development, and resulted in a significant dose-dependent improvement outside the expected disease progression in untreated Mtm1-/y mice. This provides an example of optimizing disease analysis and testing therapeutic efficacy in a preclinical model, which can be applied by scientists testing therapeutic approaches using neuromuscular disease models in different laboratories. This article has an associated First Person interview with the joint first authors of the paper.

Indexed as

Myopathies, Structural, CongenitalProtein Tyrosine Phosphatases, Non-ReceptorAnimalsDisease ProgressionDynamin IIHumansMiceMuscle, SkeletalMutationPhenotypeReproducibility of ResultsDynamin IIProtein Tyrosine Phosphatases, Non-ReceptorAntisense oligonucleotideCentronuclear myopathyDynaminMyotubular myopathyNeuromuscular disorderPreclinical disease modelTherapy

Identifiers

PMID35642830
PMCPMC9346515

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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.