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Risk factor of non-tuberculous Mycobacterium infection in patients with rheumatoid arthritis and other autoimmune diseases receiving biologic agents: A multicenter retrospective study.
Ashizawa, Hiroki; Takazono, Takahiro; Kawashiri, Shin-Ya; Nakada, Nana; Ito, Yuya; Ashizawa, Nobuyuki; Hirayama, Tatsuro; Yoshida, Masataka; Takeda, Kazuaki; Iwanaga, Naoki; Takemoto, Shinnosuke; Ide, Shotaro; Mihara, Tomo; Tomari, Shinya; Sakamoto, Noriho; Obase, Yasushi; Izumikawa, Koichi; Yanagihara, Katsunori; Kawakami, Atsushi; Mukae, Hiroshi.
Afiliación
  • Ashizawa H; Department of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Takazono T; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan; Department of Infectious Diseases, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan. Electronic address: takahiro-takazono@nagasaki-u.ac.jp.
  • Kawashiri SY; Department of Immunology and Rheumatology, Nagasaki University Hospital, Nagasaki, Japan.
  • Nakada N; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Ito Y; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Ashizawa N; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan; Department of Infection Control and Education Center, Nagasaki University Hospital, Nagasaki, Japan.
  • Hirayama T; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan; Department of Pharmacotherapeutics, Nagasaki University Hospital, Nagasaki, Japan.
  • Yoshida M; Department of Respiratory Medicine, Sasebo City General Hospital, Sasebo City, Nagasaki, Japan.
  • Takeda K; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Iwanaga N; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Takemoto S; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Ide S; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan; Department of Infectious Disease Experts Training Center, Nagasaki University Hospital, Nagasaki, Japan.
  • Mihara T; Department of Respiratory Medicine, Isahaya General Hospital, Isahaya City, Nagasaki, Japan.
  • Tomari S; Department of Respiratory Medicine, Isahaya General Hospital, Isahaya City, Nagasaki, Japan.
  • Sakamoto N; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Obase Y; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Izumikawa K; Department of Infectious Diseases, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; Department of Infection Control and Education Center, Nagasaki University Hospital, Nagasaki, Japan.
  • Yanagihara K; Department of Laboratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Kawakami A; Department of Immunology and Rheumatology, Nagasaki University Hospital, Nagasaki, Japan.
  • Mukae H; Department of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
Respir Investig ; 62(3): 322-327, 2024 May.
Article en En | MEDLINE | ID: mdl-38401245
ABSTRACT

BACKGROUND:

Evidence regarding the association of the usage of biologic agents (Etanercept, Tocilizumab, adalimumab and so on), such as anti-tumor necrosis factor α, with the incidence and risk factors of non-tuberculous Mycobacteria (NTM) infection is limited. Therefore, this study aimed to investigate the incidence and risk factors of NTM and their associations with biologic agents' usage, and also investigated the potential of Mycobacterium avium complex (MAC) antibodies as a predictor of NTM infection development.

METHODS:

This retrospective study included 672 patients with autoimmune diseases from four hospitals in Nagasaki, Japan, from January 1, 2011, to June 30, 2019, who fulfilled the inclusion criteria.

RESULTS:

Of the 672 patients, 9 (1.3%) developed complicated NTM infection, including two with disseminated infection, after the introduction of biologic agents. Of the nine patients, two died due to NTM infection but none tested positive for MAC antibodies prior to initiation of biologic agents. The mortality rate was higher in patients complicated with NTM than without NTM (22.2% vs 2.6%, P = 0.024). The corticosteroids dosage at the time of initiating the biologic agents was significantly higher in the NTM group than in the non-NTM group (median, 17 mg vs 3 mg, P = 0.0038).

CONCLUSION:

In the patients undergoing therapy with biologic agents, although NTM complication was rare, it could be fatal. In particular, for patients on a relatively high dose corticosteroids, careful observation is essential for identifying NTM complication, even if the MAC antibody test is negative.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Artritis Reumatoide / Productos Biológicos / Infección por Mycobacterium avium-intracellulare / Infecciones por Mycobacterium no Tuberculosas Límite: Humans Idioma: En Revista: Respir Investig Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Asunto principal: Artritis Reumatoide / Productos Biológicos / Infección por Mycobacterium avium-intracellulare / Infecciones por Mycobacterium no Tuberculosas Límite: Humans Idioma: En Revista: Respir Investig Año: 2024 Tipo del documento: Article País de afiliación: Japón