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Myositis-specific autoantibodies and their clinical associations in idiopathic inflammatory myopathies.
Wong, Victor Tak-Lung; So, Ho; Lam, Tommy Tsz-On; Yip, Ronald Man-Lung.
Afiliación
  • Wong VT; Medicine and Geriatrics, Kwong Wah Hospital, Kowloon, Hong Kong.
  • So H; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, New Territories, Hong Kong.
  • Lam TT; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, New Territories, Hong Kong.
  • Yip RM; Medicine and Geriatrics, Kwong Wah Hospital, Kowloon, Hong Kong.
Acta Neurol Scand ; 143(2): 131-139, 2021 Feb.
Article en En | MEDLINE | ID: mdl-32762037
BACKGROUND: Myositis-specific autoantibodies (MSAs) have been found to be present predominantly in patients with idiopathic inflammatory myopathies (IIMs). This study aimed to investigate the prevalence of MSAs and their associated complications in a cohort of patients with IIMs. METHODS: This was a multicentered prospective study. Consecutive adult Chinese patients with IIMs in the regional hospitals in Hong Kong were followed up from July 2016 to January 2018. Clinical characteristics, treatment history, and disease complications were documented. A commercially available immunoblot assay was used to detect the MSAs. RESULTS: Out of the 201 patients studied, at least one MSA was found in 63.2% of patients. The most common among the identified MSAs were the anti-melanoma differentiation-associated gene 5 antibody (anti-MDA5 Ab) and the anti-transcriptional intermediary factor 1-gamma antibody (anti-TIF1-γ Ab) (both 13.9%), followed by anti-Jo-1 antibody (12.4%). Anti-MDA5 was present exclusively in dermatomyositis (DM) and was strongly associated with digital ulcers, amyopathy, and rapidly progressive interstitial lung disease (RP-ILD). Anti-TIF1γ was strongly associated with refractory rash and malignancy. Independent risk factors of RP-ILD included anti-MDA5 (OR 14.5), clinically amyopathic DM (OR 13.9), and history of pulmonary tuberculosis (OR 12.2). Cox regression analysis showed that anti-TIF1γ (HR 3.55), DM (HR 3.82), and family history of cancer (HR 3.40) were independent predictors of malignancy. CONCLUSIONS: MSA testing enables dividing of patients with IIMs into phenotypically homogeneous subgroups and prediction of potentially life-threatening complications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Autoanticuerpos / Miositis Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Acta Neurol Scand Año: 2021 Tipo del documento: Article País de afiliación: Hong Kong Pais de publicación: Dinamarca

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Autoanticuerpos / Miositis Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Acta Neurol Scand Año: 2021 Tipo del documento: Article País de afiliación: Hong Kong Pais de publicación: Dinamarca