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Protective effect of hydroxychloroquine on infections in patients with systemic lupus erythematosus: an observational study using the LUNA registry.
Hidekawa, Chiharu; Yoshimi, Ryusuke; Saigusa, Yusuke; Tamura, Jun; Kojitani, Noriko; Suzuki, Naoki; Sakurai, Natsuki; Yoshioka, Yuji; Sugiyama-Kawahara, Yumiko; Kunishita, Yosuke; Kishimoto, Daiga; Higashitani, Kana; Sato, Yuichiro; Komiya, Takaaki; Nagai, Hideto; Hamada, Naoki; Maeda, Ayaka; Tsuchida, Naomi; Hirahara, Lisa; Soejima, Yutaro; Takase-Minegishi, Kaoru; Kirino, Yohei; Yajima, Nobuyuki; Sada, Ken-Ei; Miyawaki, Yoshia; Ichinose, Kunihiro; Ohno, Shigeru; Kajiyama, Hiroshi; Sato, Shuzo; Shimojima, Yasuhiro; Fujiwara, Michio; Nakajima, Hideaki.
Afiliação
  • Hidekawa C; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Yoshimi R; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Saigusa Y; Clinical Laboratory Department, Yokohama City University Hospital, Yokohama, Japan.
  • Tamura J; Department of Biostatistics, Yokohama City University School of Medicine, Yokohama, Japan.
  • Kojitani N; Department of Biostatistics, Yokohama City University School of Medicine, Yokohama, Japan.
  • Suzuki N; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Sakurai N; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Yoshioka Y; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Sugiyama-Kawahara Y; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Kunishita Y; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Kishimoto D; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Higashitani K; Center for Rheumatic Diseases, Yokohama City University Medical Center, Yokohama, Japan.
  • Sato Y; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Komiya T; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Nagai H; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Hamada N; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Maeda A; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Tsuchida N; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Hirahara L; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Soejima Y; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Takase-Minegishi K; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Kirino Y; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Yajima N; Department of Stem Cell and Immune Regulation, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Sada KE; Division of Rheumatology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
  • Miyawaki Y; Department of Clinical Epidemiology, Kochi Medical School, Kochi University, Nankoku, Japan.
  • Ichinose K; Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Ohno S; Department of Immunology and Rheumatology, Division of Advanced Preventive Medical Sciences, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Kajiyama H; Center for Rheumatic Diseases, Yokohama City University Medical Center, Yokohama, Japan.
  • Sato S; Department of Rheumatology and Applied Immunology, Faculty of Medicine, Saitama Medical University, Morohongo, Japan.
  • Shimojima Y; Department of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Japan.
  • Fujiwara M; Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, Japan.
  • Nakajima H; Department of Rheumatology, Yokohama Rosai Hospital, Yokohama, Japan.
Front Immunol ; 14: 1227403, 2023.
Article em En | MEDLINE | ID: mdl-37720209
ABSTRACT

Objectives:

Infection is a leading cause of death in patients with systemic lupus erythematosus (SLE). Alt hough hydroxychloroquine (HCQ) has been reported to inhibit infection, evidence from Asian populations remains insufficient. We investigated this effect in Japanese SLE patients.

Methods:

Data from the Lupus Registry of Nationwide Institutions were used in this study. The patients were ≥20 years old and met the American College of Rheumatology (ACR) classification criteria revised in 1997. We defined "severe infections" as those requiring hospitalization. We analyzed the HCQ's effect on infection suppression using a generalized estimating equation (GEE) logistic regression model as the primary endpoint and performed a survival analysis for the duration until the first severe infection.

Results:

Data from 925 patients were used (median age, 45 [interquartile range 35-57] years; female, 88.1%). GEE analysis revealed that severe infections were significantly associated with glucocorticoid dose (odds ratio [OR] 1.968 [95% confidence interval, 1.379-2.810], p<0.001), immunosuppressants (OR 1.561 [1.025-2.380], p=0.038), and baseline age (OR 1.043 [1.027-1.060], p<0.001). HCQ tended to suppress severe infections, although not significantly (OR 0.590 [0.329-1.058], p=0.077). Survival time analysis revealed a lower incidence of severe infections in the HCQ group than in the non-HCQ group (p<0.001). In a Cox proportional hazards model, baseline age (hazard ratio [HR] 1.029 [1.009-1.050], p=0.005) and HCQ (HR 0.322 [0.142-0.728], p=0.006) were significantly related to incidence.

Conclusion:

HCQ may help extend the time until the occurrence of infection complications and tends to decrease infection rates.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hidroxicloroquina / Lúpus Eritematoso Sistêmico Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Middle aged Idioma: En Revista: Front Immunol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hidroxicloroquina / Lúpus Eritematoso Sistêmico Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Middle aged Idioma: En Revista: Front Immunol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão