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Lurasidone for major depressive disorder with mixed features and irritability: a post-hoc analysis.
Swann, Alan C; Fava, Maurizio; Tsai, Joyce; Mao, Yongcai; Pikalov, Andrei; Loebel, Antony.
Afiliação
  • Swann AC; 1Department of Psychiatry and Behavioral Sciences,Baylor College of Medicine,Houston,Texas.
  • Fava M; 2Department of Psychiatry,Massachusetts General Hospital,Boston,Massachusetts.
  • Tsai J; 3Sunovion Pharmaceuticals Inc.,Fort Lee,New Jersey, andMarlborough,Massachusetts.
  • Mao Y; 3Sunovion Pharmaceuticals Inc.,Fort Lee,New Jersey, andMarlborough,Massachusetts.
  • Pikalov A; 3Sunovion Pharmaceuticals Inc.,Fort Lee,New Jersey, andMarlborough,Massachusetts.
  • Loebel A; 3Sunovion Pharmaceuticals Inc.,Fort Lee,New Jersey, andMarlborough,Massachusetts.
CNS Spectr ; 22(2): 228-235, 2017 Apr.
Article em En | MEDLINE | ID: mdl-28300012
OBJECTIVE: The aim of this post-hoc analysis was to evaluate the efficacy of lurasidone in treating major depressive disorder (MDD) with mixed features including irritability. METHODS: The data in this analysis were derived from a study of patients meeting DSM-IV-TR criteria for unipolar MDD, with a Montgomery-Åsberg Depression Rating Scale (MADRS) total score ≥26, presenting with two or three protocol-defined manic symptoms, and who were randomized to 6 weeks of double-blind treatment with either lurasidone 20-60 mg/d (n=109) or placebo (n=100). We defined "irritability" as a score ≥2 on both the Young Mania Rating Scale (YMRS) irritability item (#5) and the disruptive-aggressive item (#9). Endpoint change in the MADRS and YMRS items 5 and 9 were analyzed using a mixed model for repeated measures for patients with and without irritability. RESULTS: Some 20.7% of patients met the criteria for irritability. Treatment with lurasidone was associated with a significant week 6 change vs. placebo in MADRS score in both patients with (-22.6 vs. -9.5, p<0.0001, effect size [ES]=1.4) and without (-19.9 vs. -13.8, p<0.0001, ES=0.7) irritability. In patients with irritable features, treatment with lurasidone was associated with significant week 6 changes vs. placebo in both the YMRS irritability item (-1.4 vs. -0.3, p=0.0012, ES=1.0) and the YMRS disruptive-aggressive item (-1.0 vs. -0.3, p=0.0002, ES=1.2). CONCLUSIONS: In our post-hoc analysis of a randomized, placebo-controlled, 6-week trial, treatment with lurasidone significantly improved depressive symptoms in MDD patients with mixed features including irritability. In addition, irritability symptoms significantly improved in patients treated with lurasidone.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Humor Irritável / Transtorno Depressivo Maior / Cloridrato de Lurasidona Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: CNS Spectr Assunto da revista: NEUROLOGIA Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Humor Irritável / Transtorno Depressivo Maior / Cloridrato de Lurasidona Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: CNS Spectr Assunto da revista: NEUROLOGIA Ano de publicação: 2017 Tipo de documento: Article