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Changes in prolactin in olanzapine-treated adolescents with schizophrenia or bipolar mania: A pooled analysis of 4 studies

Published online by Cambridge University Press:  16 April 2020

C. Robertson-Plouch
Affiliation:
Lilly Research Laboratories, Indianapolis, IN, USA
G. Carlson
Affiliation:
Stony Brook University School of Medicine, Stony Brook, NY, USA
M. DelBello
Affiliation:
University of Cincinnati College of Medicine, Cincinnati, OH, USA
R. Findling
Affiliation:
Case Western Reserve University, Cleveland, OH, USA
R. Kowatch
Affiliation:
University of Cincinnati College of Medicine, Cincinnati, OH, USA
S.C. Schulz
Affiliation:
University of Minnesota Medical School, Minneapolis, MN, USA
L. Kryzhanovskaya
Affiliation:
Lilly Research Laboratories, Indianapolis, IN, USA
W. Xu
Affiliation:
Lilly Research Laboratories, Indianapolis, IN, USA
J. Carlson
Affiliation:
Lilly Research Laboratories, Indianapolis, IN, USA
M. Tohen
Affiliation:
Lilly Research Laboratories, Indianapolis, IN, USA McLean Hospital, Harvard Medical School, Belmont, MA, USA

Abstract

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Introduction:

Prolactin (PRL) data from adolescents treated with olanzapine are presented.

Methods:

Data from 454 adolescents (13-18, mean=15.9 yrs) with schizophrenia or bipolar mania were pooled from 4 olanzapine (2.5-20.0mg/day) studies (4-32 weeks; 2 double-blind, placebo-controlled studies [combined for acute phase endpoint PRL levels] with open-label extensions; 2 open-label studies). Age- and sex-specific Covance reference ranges defined normal PRL; categorical increases were based on multiples of the upper limit of normal (ULN). Baseline-to-endpoint PRL changes in adolescents were compared with data pooled from 84 olanzapine clinical trials in adults with schizophrenia or bipolar disorder.

Results:

Olanzapine-treated adolescents had mean PRL increases at both the acute (11.4μg/L) and open-label endpoints (4.7μg/L). Of those patients with normal PRL levels at baseline (N=311), high PRL occurred in 54.7% at anytime; 32.2% at endpoint. The percentage of patients in which PRL levels shifted from normal-to-abnormal was smaller at endpoint than at anytime during treatment; 26.7% shifted to a higher category. Among patients with normal baseline PRL, 32.7% remained <=1X ULN; 32.3% increased to 1¬<=2X; 6.0%, >2-<=3X; and 1.2%, >3X at anytime; 4.6% had at >=1 potentially PRL-related adverse event. Adolescents had significantly higher mean changes at endpoint (p=.004), and a greater incidence of high PRL levels at anytime during olanzapine treatment (p<.001) versus adults.

Conclusion:

Incidence of high PRL was significantly higher, and mean increases in PRL were significantly greater in adolescents versus adults. Mean increases and high PRL incidence were lower at the open-label compared with the acute phase endpoint.

Type
Poster Session 1: Antipsychotic Medications
Copyright
Copyright © European Psychiatric Association 2007
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