Evidence map›Paper›PMID 40508159›Full record

ReviewInternational journal of molecular sciences2025

Multisystem Symptoms in Myotonic Dystrophy Type 1: A Management and Therapeutic Perspective.

Dhvani H Kuntawala, Rui Vitorino, Ana C Cruz, Filipa Martins, Sandra Rebelo

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

5 authors.

Dhvani H KuntawalaMedical Sciences Department, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-183 Aveiro, Portugal.ORCID 0000-0002-7813-8881
Rui VitorinoMedical Sciences Department, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-183 Aveiro, Portugal.ORCID 0000-0003-3636-5805
Ana C CruzMedical Sciences Department, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-183 Aveiro, Portugal.ORCID 0009-0000-0123-1968
Filipa MartinsMedical Sciences Department, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-183 Aveiro, Portugal.ORCID 0000-0002-3277-1809
Sandra RebeloMedical Sciences Department, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-183 Aveiro, Portugal.ORCID 0000-0002-5862-5797

Funding

Fundação para a Ciência e a tecnologia UIDB/04501/2020 and DOI identifier https://doi.org/10.54499/UIDB/04501/2020Fundação para a Ciência e a Tecnologia UIDP/04501/2020 and DOI identifier https://doi.org/10.54499/UIDP/04501/2020
6 · The paper itself

Abstract

Myotonic dystrophy type 1 (DM1) is a complex, multisystemic neuromuscular disorder with several pathological phenotypes, disease severities and ages of onset. DM1 presents significant challenges in clinical management due to its multisystemic nature, affecting multiple organs and systems beyond skeletal muscle. Tackling this condition requires a comprehensive approach that goes beyond symptom management, particularly considering the complexity of its manifestations and in the delayed diagnosis. In this review we will discuss the multisystem symptoms of DM1 and how this understanding is guiding the development of potential therapies for the improvement of patient outcomes and quality of life. This review aims to explore the available treatments and potential novel disease-modifying therapies targeting DM1 molecular mechanisms to address the broad multisystem symptoms of DM1. Effective strategies to manage symptoms remain crucial, such as physical therapy, medications for myotonia and diligent cardiac care. Metabolic management and hormonal therapies play crucial roles in addressing endocrine and metabolic abnormalities. Nevertheless, promising targeted therapies that include antisense oligonucleotides (ASOs) for RNA degradation, small molecules to disrupt protein-RNA interactions and gene editing offer a prospective approach to the underlying mechanisms of DM1 and improve patient outcomes across the different organ systems.

Indexed as

Myotonic DystrophyAnimalsDisease ManagementHumansQuality of Lifeclinical trialsdisease-modifying therapymultisystem diseasemuscular dystrophymyotonic dystrophy type 1rare disease

Identifiers

PMID40508159
PMCPMC12155408

What OpenQuestion holds

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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.