Evidence map›Paper›PMID 40826379›Full record

ArticleBMC rheumatology2025

Clinical characteristics and outcomes of anti-MDA5 dermatomyositis: a retrospective study.

Tulaton Sodsri, Tananchai Petnak, Thitiporn Suwatanapongched, Chayanin Nitiwarangkul, Nantakarn Pongtarakulpanit, Pintip Ngamjanyaporn

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Article in BMC rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Tulaton SodsriFaculty of Medicine Ramathibodi Hospital, Chakri Naruebodindra Medical Institute, Mahidol University, Samut Prakan, Thailand.
Tananchai PetnakDivision of Pulmonary and Pulmonary Critical Care Medicine, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Thitiporn SuwatanapongchedDivision of Diagnostic Radiology, Department of Diagnostic and Therapeutic Radiology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Chayanin NitiwarangkulDivision of Diagnostic Radiology, Department of Diagnostic and Therapeutic Radiology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Nantakarn PongtarakulpanitDivision of Allergy, Immunology and Rheumatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama 6 Road, Thoong Paya Thai Subdistrict, Ratchathewi District, Bangkok, 10400, Thailand.
Pintip NgamjanyapornDivision of Allergy, Immunology and Rheumatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama 6 Road, Thoong Paya Thai Subdistrict, Ratchathewi District, Bangkok, 10400, Thailand. pintip.nga@mahidol.ac.th.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnti-MDA5 dermatomyositis (anti-MDA5 DM) is a rare but severe subtype of dermatomyositis associated with high mortality. This study aimed to describe clinical characteristics and identify variables associated with rapidly progressive interstitial lung disease (RP-ILD) and mortality among affected patients.

methodsPatients diagnosed with anti-MDA5 DM between January 2013 and October 2022 were included. Demographics, clinical manifestations, and laboratory data were collected. Univariable Cox proportional hazard regression was used to assess mortality predictors, while logistic regression models identified factors associated with RP-ILD.

resultsAmong 26 patients (mean age, 56.6 ± 15.1 years, 7 men), the most common clinical manifestation was Gottrón’s papules (80.8%), followed by ILD (73.1%), periungual erythema (69.2%), heliotrope rash (61.5%), V-sign (42.3%), arthritis (42.3%), weakness (38.5%), shawl sign (34.6%), mechanic’s hand (34.6%), and Raynaud’s phenomenon (19.2%). Among 19 ILD patients, 9 (47.4%) developed RP-ILD, and seven patients died over a median follow-up of 1.5 years. The overall mortality rate in this cohort was 26.9%, with 77.8% having RP-ILD. Mortality was associated with male sex (HR, 7.7; 95% CI, 1.49–39.9; P = 0.02) and RP-ILD, which had a risk difference of 77.8 (95% CI 50.6-104.9%; P = 0.001). Arthritis (P = 0.01) and ANA positivity (P = 0.03) were associated with reduced risk of RP-ILD. Patients with RP-ILD tended to receive aggressive treatments, including triple therapy regimens (55.6%), which consisted of a combination of intravenous methylprednisolone and intravenous cyclophosphamide with either rituximab or a calcineurin inhibitor. Additional treatments included intravenous immunoglobulin (22.2%) and plasma exchange (33.3%).

conclusionAnti-MDA5 DM was associated with a high prevalence of ILD, particularly RP-ILD, contributing to increased mortality, underscoring the need for early identification of high-risk patients and personalized management. TAKE-HOME MESSAGE: Male sex was a key predictor of RP-ILD and poor prognosis in anti-MDA5 dermatomyositis patients. Conversely, arthritis and ANA positivity might be associated with a lower risk of RP-ILD. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

DermatomyositisInterstitial lung diseaseMDA5 autoantibodyMortalityRapidly progressive interstitial lung disease

Identifiers

PMID40826379
PMCPMC12359913

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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.