Evidence map›Paper›PMID 39973455›Full record

ReviewJournal of neuromuscular diseases

Exploring the therapeutic potential of fibroadipogenic progenitors in muscle disease.

Marshall W Hogarth, Medha P Kurukunda, Karim Ismat, Prech Uapinyoying, Jyoti K Jaiswal

Abstract readReview
In one paragraph

Review in Journal of neuromuscular diseases. 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. Review
  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.

Marshall W HogarthCenter for Genetic Medicine Research, Children's National Research Institute, Washington, DC, USA.
Medha P KurukundaCenter for Genetic Medicine Research, Children's National Research Institute, Washington, DC, USA.
Karim IsmatCenter for Genetic Medicine Research, Children's National Research Institute, Washington, DC, USA.
Prech UapinyoyingCenter for Genetic Medicine Research, Children's National Research Institute, Washington, DC, USA.
Jyoti K JaiswalCenter for Genetic Medicine Research, Children's National Research Institute, Washington, DC, USA.

Funding

Understanding the mechanism and role of cell membrane repair in Miyoshi MyopathyR01AR055686 · NIAMS · ROCKEFELLER UNIVERSITY · PI JAISWAL, JYOTI K · 2008 to 2021
$3.6M
Modulating Fibro/Adipogenic Precursors to Prevent Adipogenic Replacement of MuscleK01AR077686 · NIAMS · CHILDREN'S RESEARCH INSTITUTE · PI HOGARTH, MARSHALL · 2021 to 2025
$497k
NIAMS NIH HHS K01 AR077686NIAMS NIH HHS R01 AR055686
6 · The paper itself

Abstract

Skeletal muscle relies on its inherent self-repair ability to withstand continuous mechanical damage. Myofiber-intrinsic processes facilitate the repair of damage to sarcolemma and sarcomeres, but it is the coordinated interaction between muscle-resident satellite and stromal cells that are crucial in the regeneration of muscles to replace the lost muscle fibers. Fibroadipogenic progenitors (FAPs), are muscle-resident mesenchymal cells that are notable for their role in creating the dynamic stromal niche required to support long-term muscle homeostasis and regeneration. While FAP-mediated extracellular matrix formation and the establishment of a homeostatic muscle niche are essential for maintaining muscle health, excessive accumulation of FAPs and their aberrant differentiation leads to the fibrofatty degeneration that is a hallmark of myopathies and muscular dystrophies. Recent advancements, including single-cell RNA sequencing and

Indexed as

Mesenchymal Stem CellsMuscle, SkeletalMuscular DiseasesAnimalsHumansRegenerationadipogenesisfibroadipogenicfibrosismesenchymal stem cellsmusclemuscular dystrophyregeneration

Identifiers

PMID39973455
PMCPMC11949306

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.