Evidence map›Paper›PMID 36076964›Full record

ArticleInternational journal of molecular sciences2022

Exploring the Therapeutic Potential of Ectoine in Duchenne Muscular Dystrophy: Comparison with Taurine, a Supplement with Known Beneficial Effects in the

Caroline Merckx, Jana Zschüntzsch, Stefanie Meyer, Robrecht Raedt, Hanne Verschuere, Jens Schmidt, Boel De Paepe, Jan L De Bleecker

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. New Pharmacological Approaches for Rare Diseases.International journal of molecular sciences · 2023
    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

8 authors at 3 institutions in 2 countries.

Caroline MerckxDepartment of Neurology, Ghent University and Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0002-9031-2539
Jana ZschüntzschDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.ORCID 0000-0002-7062-5319
Stefanie MeyerDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Robrecht Raedt4BRAIN, Department Head and Skin, Ghent University, 9000 Ghent, Belgium.ORCID 0000-0002-8939-0169
Hanne VerschuereUnit of Molecular Signaling and Cell Death, Center for Inflammation Research, Flemish Institute for Biotechnology, 9052 Ghent, Belgium.ORCID 0000-0003-1605-6618
Jens SchmidtDepartment of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Boel De PaepeDepartment of Neurology, Ghent University and Ghent University Hospital, 9000 Ghent, Belgium.ORCID 0000-0001-9403-4401
Jan L De BleeckerDepartment of Neurology, Ghent University and Ghent University Hospital, 9000 Ghent, Belgium.
Ghent University Hospital · BEUniversitätsmedizin Göttingen · DEGhent University · BE

Funding

Association Belge Contre les Maladies Neuro-Musculaires NAEuropean Joint Programme on Rare Diseases (EJP-RD) NAU4-society Network OSMYO NA
6 · The paper itself

Abstract

Duchenne Muscular Dystrophy (DMD) is a debilitating muscle disorder that condemns patients to year-long dependency on glucocorticoids. Chronic glucocorticoid use elicits many unfavourable side-effects without offering satisfying clinical improvement, thus, the search for alternative treatments to alleviate muscle inflammation persists. Taurine, an osmolyte with anti-inflammatory effects, mitigated pathological features in the

Indexed as

Muscular Dystrophy, DuchenneAmino Acids, DiaminoAnimalsDisease Models, AnimalMiceMice, Inbred C57BLMice, Inbred mdxMuscle, SkeletalTaurineAmino Acids, DiaminoectoineTaurineDuchenneectoinehistopathologymdxosmolytetaurine

Identifiers

PMID36076964
PMCPMC9455265
OpenAlexW4292998842

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.