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Prognosis of spontaneous pneumomediastinum occurring in dermatomyositis or polymyositis patients with interstitial lung disease according to antimelanoma differentiation-associated gene 5 antibody status: a retrospective cohort study.
Abe, Kazuya; Furuta, Shunsuke; Kobayashi, Yoshihisa; Sugiyama, Takao; Kagami, Shin-Ichiro; Nakagomi, Daiki; Iwamoto, Taro; Ikeda, Kei; Nakajima, Hiroshi.
Afiliación
  • Abe K; Department of Allergy and Clinical Immunology, Chiba University Hospital, Chiba, Japan.
  • Furuta S; Department of Allergy and Clinical Immunology, Chiba University Hospital, Chiba, Japan shfuruta@chiba-u.jp.
  • Kobayashi Y; Department of Internal Medicine, Chiba Aoba Municipal Hospital, Chiba, Japan.
  • Sugiyama T; Department of Rheumatology, National Hospital Organization Shimoshizu Hospital, Yotsukaido, Chiba, Japan.
  • Kagami SI; Research Center for Allergy and Clinical Immunology, Asahi General Hospital, Asahi, Chiba, Japan.
  • Nakagomi D; Third Department of Internal Medicine, University of Yamanashi Hospital, Chuo, Japan.
  • Iwamoto T; Department of Allergy and Clinical Immunology, Chiba University Hospital, Chiba, Japan.
  • Ikeda K; Department of Allergy and Clinical Immunology, Chiba University Hospital, Chiba, Japan.
  • Nakajima H; Department of Allergy and Clinical Immunology, Chiba University Hospital, Chiba, Japan.
RMD Open ; 9(1)2023 02.
Article en En | MEDLINE | ID: mdl-36759007
ABSTRACT

OBJECTIVES:

Spontaneous pneumomediastinum (SPNM) historically has been considered a poor prognostic factor in dermatomyositis/polymyositis patients complicated with interstitial lung disease (ILD). However, there is a lack of actual data regarding the association between SPNM occurrence and mortality in dermatomyositis/polymyositis patients. This study aimed to assess the association between SPNM occurrence and mortality in myositis patients with ILD according to antimelanoma differentiation-associated gene 5 (MDA5) antibody status.

METHODS:

Dermatomyositis/polymyositis patients with ILD who were hospitalised at five Japanese hospitals from 2016 to 2020 were included in this retrospective observational study. We collected data about baseline characteristics including myositis-specific autoantibodies, treatments, SPNM and death within 1 year from therapy initiation or strengthening. Baseline characteristics and outcomes were compared between patients with and without SPNM (the SPNM group and the non-SPNM group, respectively).

RESULTS:

A total of 119 patients were analysed. SPNM occurred in 23 patients, and 15 patients died. Fifteen patients with SPNM were anti-MDA5 antibody positive. The mortality rate was significantly higher in the SPNM group (34.8%) than in the non-SPNM group (7.3%) (p=0.001). All deaths in the SPNM group occurred in anti-MDA5 antibody-positive patients (8/15), whereas none of the anti-MDA5 antibody-negative patients in the SPNM group died (0/8). In anti-MDA5 antibody-positive patients, the mortality rate was significantly higher in patients with SPNM occurrence (53.3%) than in those without SPNM occurrence (4.0%) (p=0.001).

CONCLUSION:

SPNM occurred more frequently in anti-MDA5 antibody-positive than in anti-MDA5 antibody-negative myositis patients. SPNM occurrence was associated with higher mortality risk, especially in anti-MDA5 antibody-positive patients.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polimiositis / Enfermedades Pulmonares Intersticiales / Dermatomiositis / Enfisema Mediastínico / Miositis Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: RMD Open Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polimiositis / Enfermedades Pulmonares Intersticiales / Dermatomiositis / Enfisema Mediastínico / Miositis Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: RMD Open Año: 2023 Tipo del documento: Article País de afiliación: Japón