Evidence map›Paper›PMID 40649771›Full record

ArticleInternational journal of molecular sciences2025

Profiles of Monocyte Subsets and Fibrosis-Related Genes in Patients with Muscular Dystrophy Undergoing Intermittent Prednisone Therapy.

Asma Chikhaoui, Dorra Najjar, Sami Bouchoucha, Rim Boussetta, Nadia Ben Achour, Kalthoum Tizaoui, Ichraf Kraoua, Ilhem Turki, Houda Yacoub-Youssef

Abstract read
In one paragraph

Article 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Asma ChikhaouiLaboratory of Biomedical Genomics and Oncogenetics (LR16IPT05), Institut Pasteur de Tunis, Université Tunis El Manar, El Manar I, Tunis 2092, Tunisia.
Dorra NajjarLaboratory of Biomedical Genomics and Oncogenetics (LR16IPT05), Institut Pasteur de Tunis, Université Tunis El Manar, El Manar I, Tunis 2092, Tunisia.
Sami BouchouchaService Orthopédie, Hôpital d'enfant Béchir Hamza, Tunis 1007, Tunisia.
Rim BoussettaService Orthopédie, Hôpital d'enfant Béchir Hamza, Tunis 1007, Tunisia.
Nadia Ben AchourLR18SP04, Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis 1007, Tunisia.
Kalthoum TizaouiLaboratory of Biomedical Genomics and Oncogenetics (LR16IPT05), Institut Pasteur de Tunis, Université Tunis El Manar, El Manar I, Tunis 2092, Tunisia.
Ichraf KraouaLR18SP04, Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis 1007, Tunisia.
Ilhem TurkiLR18SP04, Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis 1007, Tunisia.
Houda Yacoub-YoussefLaboratory of Biomedical Genomics and Oncogenetics (LR16IPT05), Institut Pasteur de Tunis, Université Tunis El Manar, El Manar I, Tunis 2092, Tunisia.ORCID 0000-0001-5351-4775

Funding

Acip_Myopath The impact of micro-RNAs and inflammatory pathways on stem cell fate and the regenerative process in human inherited muscle diseases 2015-2017Tunisian Ministry of Higher Education and Scientific Research LR16IPT05
6 · The paper itself

Abstract

Muscle dystrophies are a group of genetic disorders characterized by progressive muscle degeneration. Prednisone is a glucocorticoid drug widely used to prevent muscle weakness in these diseases. Despite its known beneficial role, the effect of intermittent delivery on monocytes' polarization and on dystrophic muscle microenvironment has not yet been thoroughly investigated. In this study, our aim was to identify the phenotype of monocyte subsets in blood and the expression of fibrosis-related genes in dystrophic muscle biopsies in patients receiving intermittent prednisone therapy. We found an increased rate of classical monocytes and a decreased rate of non-classical monocytes that expressed anti-inflammatory marker CD206 in treated patients. In dystrophic muscles, 21 fibrosis-related genes were altered, among which we identified CCAAT/enhancer-binding protein beta

Indexed as

MonocytesMuscular DystrophiesPrednisoneAdolescentAdultFemaleFibrosisHumansMaleMiddle AgedMuscle, SkeletalYoung AdultPrednisonegene expressionmonocyte phenotypesmuscle dystrophiesprednisone

Identifiers

PMID40649771
PMCPMC12250195

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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.