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Unique characteristics of anti-MDA-5 associated dermatomyositis in Southern California with a large Hispanic population.
Alhassan, Eaman; Yi, Belina Y; Rodman, Jack; Weisman, Michael H; Crew, Ashley; Wise, Leanna.
Afiliação
  • Alhassan E; Division of Rheumatology, Department of Medicine, University of Southern California Keck School of Medicine, Los Angeles, CA, USA. Electronic address: eaman.alhassan@med.usc.edu.
  • Yi BY; Division of Rheumatology, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, USA; Division of Pediatric Allergy, Immunology, and Rheumatology, Department of Pediatrics, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Rodman J; Clinical & Translational Science Institute, University of Southern California, Los Angeles, CA, USA.
  • Weisman MH; Division of Rheumatology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
  • Crew A; Department of Dermatology, University of Southern California Keck School of Medicine, Los Angeles, CA, USA.
  • Wise L; Division of Rheumatology, Department of Medicine, University of Southern California Keck School of Medicine, Los Angeles, CA, USA.
Semin Arthritis Rheum ; 66: 152434, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38503149
ABSTRACT

OBJECTIVES:

There is little to no data about the presentation and clinical course of anti-melanoma differentiation-associated gene-5 antibody (anti-MDA-5) dermatomyositis in a primarily U.S. Hispanic population. We describe the clinical course of anti-MDA-5 dermatomyositis in our majority Hispanic population.

METHODS:

This is a multicenter, retrospective case series of anti-MDA-5 dermatomyositis. Patients diagnosed with anti-MDA-5 dermatomyositis from June 2015 to March 2023 at four medical centers in Los Angeles, California, were included. Demographics and clinical characteristics were obtained. Descriptive statistics, Pearson's chi-squared, Fisher's exact, Wilcoxon rank sum, and Kruskal-Wallis tests were performed as applicable.

RESULTS:

Thirty anti-MDA-5 dermatomyositis patients were included. Twenty-two (73 %) were Hispanic. Twenty-one patients (70 %) were female, with a median age of 40.5 years. Hispanic patients were diagnosed with anti-MDA-5 dermatomyositis at a younger age than non-Hispanic patients (p = 0.025). Inflammatory arthritis was prominent; more males were affected than females (p = 0.027). Thirteen patients (43 %) were amyopathic. Twenty-five patients (83.3 %) had evidence of interstitial lung disease (ILD), and a higher ferritin level was associated with ILD (p = 0.049). There were six deaths (20 %); five (17 %) were ascribed to rapidly progressive ILD.

CONCLUSION:

ILD was the most common presentation of anti-MDA-5 dermatomyositis in our cohort and was associated with higher ferritin levels. Hispanic patients had a younger age of diagnosis than non-Hispanic patients. Necrotic skin lesions and inflammatory arthritis were frequently seen. This is the first study looking at clinical phenotypes and outcomes of anti-MDA-5 dermatomyositis in a primarily Hispanic U.S. POPULATION Future studies are needed to better understand the clinical manifestations (to promptly recognize and treat) of this population of anti-MDA-5 dermatomyositis.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hispânico ou Latino / Dermatomiosite / Helicase IFIH1 Induzida por Interferon Limite: Adult / Female / Humans / Male / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hispânico ou Latino / Dermatomiosite / Helicase IFIH1 Induzida por Interferon Limite: Adult / Female / Humans / Male / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2024 Tipo de documento: Article