Evidence map›Paper›PMID 38396646›Full record

ReviewInternational journal of molecular sciences2024

Extracellular Vesicles in the Pathogenesis, Clinical Characterization, and Management of Dermatomyositis: A Narrative Review.

Cristina Ricco, Ahmed Eldaboush, Ming-Lin Liu, Victoria P Werth

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. 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
1.9field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Characterizing Keratinocyte-Derived Extracellular Vesicles in UVB-Irradiated Murine Skin.JID innovations : skin science from molecules to population health · 2026
    Article
  3. Review
  4. Review
  5. Plasma Microvesicles May Contribute to Muscle Damage in theInternational journal of molecular sciences · 2025
    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

4 authors at 1 institution in 1 country.

Cristina Ricco *Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA 19104, USA.
Ahmed Eldaboush *Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA 19104, USA.ORCID 0009-0009-6699-5956
Ming-Lin LiuCorporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA 19104, USA.ORCID 0000-0001-8827-2024
Victoria P WerthCorporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA 19104, USA.
Philadelphia VA Medical Center · US

Funding

A nonpsychoactive cannabinoid receptor-2 agonist to treat itch and inflammation in dermatomyositisR01AR076766 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI WERTH, VICTORIA P · 2020 to 2023
$1.7M
Extracellular vesicle-associated MAVS and IFNẞ in DermatomyositisR21AI144838 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI LIU, MING-LIN · 2019 to 2020
$443k
BLRD VA I01 BX005921NIAMS NIH HHS R01 AR076766NIH HHS R21AI144838
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are lipid-bilayer particles secreted from cells that primarily assist in cell-to-cell communication through the content of their cargo, such as proteins and RNA. EVs have been implicated in the pathogenesis of various autoimmune diseases, including dermatomyositis (DM), an inflammatory autoimmune disease characterized by distinct cutaneous manifestations, myopathy, and lung disease. We sought to review the role of EVs in DM and understand how they contribute to the pathogenesis and clinical characterization of the disease. We summarized the research progress on EVs in dermatomyositis based on recent publications. EV cargoes, such as double-stranded DNA, microRNA, and proteins, contribute to DM pathogenesis and mediate the proinflammatory response and cytokine release through signaling pathways such as the stimulator of interferon genes (STING) pathway. These nucleic acids and proteins have been proposed as disease-specific, stable biomarkers to monitor disease activity and responses to therapy. They also correlate with clinical parameters, inflammatory markers, and disease severity scores. Furthermore, some markers show an association with morbidities of DM, such as muscle weakness and interstitial lung disease. The continued study of EVs will help us to further elucidate our understanding of dermatomyositis.

Indexed as

DermatomyositisExosomesExtracellular VesiclesLung Diseases, InterstitialMicroRNAsNucleic AcidsHumansProteinsMicroRNAsNucleic AcidsProteinsautoimmune diseasedermatomyositisexosomesextracellular vesiclesinflammatory myopathymicroparticlesmicrovesicles

Identifiers

PMID38396646
PMCPMC10889219
OpenAlexW4391575612

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.