Evidence map›Paper›PMID 39717688›Full record

ArticleSAGE open medical case reports2024

Two case reports of MDA5-type seronegative dermatomyositis.

Lauren C Balogh, Airiss R Chan, Elaine A Yacyshyn, Robert Gniadecki

Abstract readCase Reports
In one paragraph

Article in SAGE open medical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Lauren C BaloghFaculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.ORCID https://orcid.org/0009-0005-3418-640X
Airiss R ChanDivision of Dermatology, Department of Medicine, University of Alberta, Edmonton, AB, Canada.
Elaine A YacyshynDivision of Rheumatology, Department of Medicine, University of Alberta, Edmonton, AB, Canada.
Robert GniadeckiDivision of Dermatology, Department of Medicine, University of Alberta, Edmonton, AB, Canada.ORCID https://orcid.org/0000-0002-2310-8300

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dermatomyositis (DM) is an autoimmune idiopathic inflammatory myopathy with characteristic dermatologic manifestations. Myositis-specific autoantibodies (MSAs) delineate DM subtypes and their prognoses. Uncommonly, patients present with distinct clinical features of DM, including photosensitive dermatitis, heliotrope rash, Gottron's papules, and nailfold changes; however, their autoimmune serology is negative for expected MSAs. Herein, we describe two unconventional cases of seronegative, amyopathic MDA5-DM and offer potential explanations, including fluctuating antibody levels, non-MSA pathophysiology, and limitations in current immunoassays.

Indexed as

autoimmuneDermatomyositisMDA5seronegative

Identifiers

PMID39717688
PMCPMC11664525

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.