Adjunctive aripiprazole in the treatment of risperidone-induced hyperprolactinemia: A randomized, double-blind, placebo-controlled, dose–response study. (August 2015)

• Record Type: Journal Article
• Authors: Chen, Jing-Xu; Su, Yun-Ai; Bian, Qing-Tao; Wei, Li-He; Zhang, Rong-Zhen; Liu, Yan-Hong; Correll, Christoph; Soares, Jair C.; Yang, Fu-De; Wang, Shao-Li; Zhang, Xiang-Yang
• Is Part Of: Psychoneuroendocrinology. Volume 58(2015:Aug.)
• Page Start: 130
• Page End: 140
• Publication Date: 2015-08
• Subjects: Risperidone -- Aripiprazole -- Prolactin -- Hyperprolactinemia -- Intervention -- Placebo controlled trial -- Dose effect; Psychoneuroendocrinology -- Periodicals; Endocrinology -- Periodicals; Neurology -- Periodicals; Psychiatry -- Periodicals; Neuropsychoendocrinologie -- Périodiques; 616.8
• DOI: 10.1016/j.psyneuen.2015.04.011
• Languages: English
• ISSNs: 0306-4530

Abstract

Highlights: Risperidone-induced hyperprolactinemia was treated with placebo, 5, 10 or 20 mg/day aripiprazole. After 8-week treatment, all three doses lower prolactin levels significantly in schizophrenia. Effects were significantly greater in the 10 and 20 mg/day than the 5 mg/day groups. Prolactin levels decreased significantly at week 2 in all three dose groups. Aripiprazole was effective and safe for resolving comorbid hyperprolactinemia. Summary: Hyperprolactinemia is an unwanted adverse effect associated with several antipsychotics. The addition of partial dopamine receptor agonist aripiprazole may attenuate antipsychotic-induced hyperprolactinemia effectively. However, the ideal dosing regimen for this purpose is unknown. We aimed to evaluate the dose effects of adjunctive treatment with aripiprazole on prolactin levels and hyperprolactinemia in schizophrenia patients. Stable subjects 18–45 years old with schizophrenia and hyperprolactinemia (i.e., >24 ng/ml for females and >20 ng/ml for males) were randomly assigned to receive 8 weeks of placebo ( n = 30) or oral aripiprazole 5 mg/day ( n = 30), 10 mg/day ( n = 29), or 20 mg/day ( n = 30) added on to fixed dose risperidone treatment. Serum prolactin levels were measured at baseline and after 2, 4 and 8 weeks; clinical symptoms and side effects were assessed at baseline and week 8 using the Positive and Negative Syndrome Scale, Clinical Global Impressions Severity scale, Barnes Akathisia Scale, Simpson-Angus Scale and UKU Side Effects Rating Scale. Of 119 randomized patients, 107 (89.9%) completed the 8-week study. At study end, all three aripiprazole doses resulted in significantly lower prolactin levels (beginning at week 2), higher response rates (≥30% prolactin reduction) and higher prolactin normalization rates than placebo. Effects were significantly greater in the 10 and 20 mg/day groups than the 5 mg/day group. No significant changes were observed in any treatment groups regarding psychopathology and adverse effect ratings. Adjunctive aripiprazole treatment was effective and safe for resolving risperidone-induced hyperprolactinemia, producing significant and almost maximal improvements by week 2 without significant effects on psychopathology and side effects.