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Association of erythrocyte methotrexate-polyglutamate levels with the efficacy and hepatotoxicity of methotrexate in patients with rheumatoid arthritis: a 76-week prospective study.
Takahashi, Chihiro; Kaneko, Yuko; Okano, Yutaka; Taguchi, Hiroaki; Oshima, Hisaji; Izumi, Keisuke; Yamaoka, Kunihiro; Takeuchi, Tsutomu.
Afiliação
  • Takahashi C; Division of Rheumatology, Department of Internal Medicine , Keio University School of Medicine , Tokyo , Japan.
  • Kaneko Y; Division of Rheumatology, Department of Internal Medicine , Keio University School of Medicine , Tokyo , Japan.
  • Okano Y; Department of Internal Medicine and Center for Arthritis and Rheumatic Disease , Kawasaki Municipal Kawasaki Hospital , Kawasaki , Japan.
  • Taguchi H; Department of Internal Medicine and Center for Arthritis and Rheumatic Disease , Kawasaki Municipal Kawasaki Hospital , Kawasaki , Japan.
  • Oshima H; Department of Connective Tissue Diseases , Tokyo Medical Center, National Hospital Organization , Tokyo , Japan.
  • Izumi K; Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan; Department of Connective Tissue Diseases, Tokyo Medical Center, National Hospital Organization, Tokyo, Japan.
  • Yamaoka K; Division of Rheumatology, Department of Internal Medicine , Keio University School of Medicine , Tokyo , Japan.
  • Takeuchi T; Division of Rheumatology, Department of Internal Medicine , Keio University School of Medicine , Tokyo , Japan.
RMD Open ; 3(1): e000363, 2017.
Article em En | MEDLINE | ID: mdl-28123781
OBJECTIVE: To assess the utility of erythrocyte methotrexate-polyglutamate (MTX-PG) concentrations in determining the safety and efficacy of MTX in patients with rheumatoid arthritis (RA). METHODS: 79 MTX-naïve patients with RA were enrolled in this prospective 76-week cohort study. MTX was initiated, and a predefined dose-escalation protocol was followed. Erythrocyte MTX-PG concentrations were measured using liquid chromatography. The associations of MTX-PG concentrations with disease activity and adverse events were analysed. RESULTS: Dose escalation of MTX resulted in increased MTX-PG concentrations and a decrease in the mean Disease Activity Score in 28 joints (DAS28). A significant association was observed between total MTX-PG concentrations and ΔDAS28 at week 12 (ß=-0.013, p=0.003) and at week 24 (ß=-0.014, p=0.003). The maximum MTX-PG levels were significantly higher in patients presenting with elevated transaminases (≥100 IU/L) than in those without (146 vs 106 nmol/L, p=0.009). Receiver operating characteristic curve analysis revealed that a total MTX-PG concentrations of 83 nmol/L at week 12 was the threshold for a DAS28 improvement of ≥1.2 at week 24, and 105 nmol/L was the threshold for transaminases of ≥50 IU/L and 131 nmol/L for transaminases of ≥100 IU/L. MTX-PG concentrations were strongly influenced by body mass index and a serum albumin level. CONCLUSIONS: MTX-PG concentrations are a useful biomarker in MTX therapy, in terms of efficacy and safety.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Idioma: En Revista: RMD Open Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Idioma: En Revista: RMD Open Ano de publicação: 2017 Tipo de documento: Article