Effects of Short- and Long-Term Risperidone Treatment on Prolactin Levels in Children with Autism

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Abstract

Background: The effects of short- and long-term risperidone treatment on serum prolactin were assessed in children and adolescents with autism. Methods: Patients with autism (N = 101, 5-17 years of age) were randomized to an 8-week trial of risperidone or placebo and 63 then took part in a 4-month open-label follow-up phase. Serum samples were obtained at Baseline and Week-8 (N = 78), and at 6-month (N = 43) and 22-month (N = 30) follow-up. Serum prolactin was determined by immunoradiometric assay; dopamine type-2 receptor (DRD2) polymorphisms were genotyped. Results: Baseline prolactin levels were similar in the risperidone (N = 42) and placebo (N = 36) groups (9.3 ± 7.5 and 9.3 ± 7.6 ng/ml, respectively). After 8 weeks of risperidone, prolactin increased to 39.0 ± 19.2 ng/ml, compared with 10.1 ± 8.8 ng/ml for placebo (p

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Anderson, G. M., Scahill, L., McCracken, J. T., McDougle, C. J., Aman, M. G., Tierney, E., … Vitiello, B. (2007). Effects of Short- and Long-Term Risperidone Treatment on Prolactin Levels in Children with Autism. Biological Psychiatry, 61(4), 545–550. https://doi.org/10.1016/j.biopsych.2006.02.032

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