Triiodothyronine accelerates and enhances the antipsychotic effect of risperidone in acute schizophrenia

التفاصيل البيبلوغرافية
العنوان: Triiodothyronine accelerates and enhances the antipsychotic effect of risperidone in acute schizophrenia
المؤلفون: Adomas Bunevicius, Arunas Savickas, Vesta Steibliene, Robertas Bunevičius, Charles B. Nemeroff, Arthur J. Prange
المصدر: Journal of psychiatric research. 73
سنة النشر: 2015
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, medicine.medical_treatment, Placebo, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Internal medicine, Brief Psychiatric Rating Scale, medicine, Humans, Single-Blind Method, Psychiatry, Antipsychotic, Biological Psychiatry, Retrospective Studies, Psychiatric Status Rating Scales, Analysis of Variance, Risperidone, Retrospective cohort study, Drug Synergism, Middle Aged, medicine.disease, 030227 psychiatry, Psychiatry and Mental health, Treatment Outcome, Tolerability, Schizophrenia, Clinical Global Impression, Regression Analysis, Triiodothyronine, Female, Psychology, 030217 neurology & neurosurgery, medicine.drug, Antipsychotic Agents
الوصف: In acute psychotic schizophrenia patients we investigated if the combination of triiodothyronine (T3) plus risperidone was more effective when compared to risperidone monotherapy. Thirty-two in-patients meeting the DSM-IV-TR diagnostic criteria for schizophrenia and without thyroid disease received risperidone (flexibly adjusted dose for tolerability) and were randomized to additionally receive either T3 (25 μg daily; risperidone plus T3 group) or placebo (risperidone plus placebo group). Treatment lasted until meeting the response to treatment criteria defined as score of ≤ 3 on the Clinical Global Impression Severity and Improvement scales. Acute psychotic episode symptom severity was evaluated using the Brief Psychiatric Rating Scale (BPRS) at treatment initiation and at the final study assessment. Fourteen patients were randomized to receive risperidone plus T3 and eighteen to receive risperidone plus placebo. The time until treatment response was shorter in the risperidone plus T3 group relative to the risperidone plus placebo group (25.5 ± 4.4 days vs 32.2 ± 8.2 days, respectively; p = 0.001). Moreover, there was a greater reduction of BPRS-total score (p = 0.01) in the risperidone plus T3 group relative to the risperidone plus placebo group. Treatment with T3 was associated with shorter time to treatment response (β = -0.440, p = 0.022) and with greater improvement in BPRS score (β = 0.240, p = 0.053), independent of patients' gender, age, baseline BPRS score and mean risperidone dose. The study confirms that addition of T3 to risperidone was associated with accelerated and enhanced treatment response in acutely psychotic schizophrenic patients.
تدمد: 1879-1379
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168093ab7d14499eb6da3bde8c14bb01
https://pubmed.ncbi.nlm.nih.gov/26679760
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....168093ab7d14499eb6da3bde8c14bb01
قاعدة البيانات: OpenAIRE