Evidence map›Paper›PMID 24803842›Full record

ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2013

Eosinophils in hereditary and inflammatory myopathies.

Thomas Schröder, Johann Fuchss, Ilka Schneider, Gisela Stoltenburg-Didinger, Frank Hanisch

Abstract read
In one paragraph

Article in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Compositional and Functional MRI of Skeletal Muscle: A Review.Journal of magnetic resonance imaging : JMRI · 2024
    Review
  5. Article
  6. Article
  7. Eosinophilic Orbital Myositis Superseding Ocular Myasthenia.Mediterranean journal of rheumatology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Characterization of a mouse model of hypereosinophilia-associated heart disease.American journal of physiology. Heart and circulatory physiology · 2019
    Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Myositis Mimics.Current rheumatology reports · 2015
    Review
  17. Article
  18. 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 at 1 institution in 1 country.

Thomas SchröderDepartment of Neurology, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany;
Johann FuchssDepartment of Neurology, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany;
Ilka SchneiderDepartment of Neurology, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany;
Gisela Stoltenburg-DidingerInstitute of Cell Biology and Neurobiology, Charité, Universitätsmedizin Berlin, Germany.
Frank HanischDepartment of Neurology, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany;
Martin Luther University Halle-Wittenberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is not known whether eosinophilic myositis is a specific histopathological feature of limb girdle muscular dystrophy 2A (LGMD2A). Number and location of eosinophils in skeletal muscle biopsies (n=100) was analysed by Giemsa and modified hematoxylin/eosin staining in patients with genetically confirmed myopathies (LGMD2A, LGMD2B, LGMD2L, facioscapulohumeral muscular dystrophy, dystrophinopathy), histologically confirmed idiopathic inflammatory myopathies (sporadic inclusion body myositis (sIBM), dermatomyositis (DM), polymyositis), amyotrophic lateral sclerosis (neurogenic control), and normal controls. The number of eosinophils/mm² was significantly higher in LGMD2A, PM, DM, and sIBM compared to controls but not significantly higher than other myopathies. A large overlap in the number of eosinophils/mm2 between all groups was seen. In all disease groups eosinophils were mainly found endomysially (46- 88%) and intra- and perivascularly (4-37%). There was no correlation between the numbers of eosinophils/mm² and (i) age at biopsy and (ii) the duration of the disease. The extent of myopathic, fibrotic, and inflammatory changes did not differ in samples with high and low eosinophil count. Eosinophils seem to represent an unspecific histological finding in hereditary and inflammatory myopathies, but also amyotrophic lateral sclerosis.

Indexed as

AdolescentAdultAgedBiopsyChildChild, PreschoolEosinophiliaFemaleGermanyHumansInfantMaleMiddle AgedMuscular Dystrophies, Limb-GirdleMyositisStaining and Labelingamyotrophic lateral sclerosiscalpainopathyEosinophilGiemsa staininghereditary myopathyinflammatory myopathylimb girdle muscular dystrophy

Identifiers

PMID24803842
PMCPMC4006278
OpenAlexW130553249

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.