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Changes in metabolic parameters in olanzapine-treated adolescents with schizophrenia or bipolar I disorder: A pooled analysis of 4 studies

Published online by Cambridge University Press:  16 April 2020

L. Kryzhanovskaya
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
C. Robertson-Plouch
Affiliation:
Lilly Research Laboratories, Indianapolis, IN, USA
W. Xu
Affiliation:
Lilly Research Laboratories, Indianapolis, IN, USA
G. Sethuraman
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:

The changes in metabolic parameters in olanzapine-treated adolescents were examined.

Methods:

Data from 454 adolescents (13–18, mean=15.9 years) with schizophrenia or bipolar I disorder were pooled from 4 olanzapine (2.5–20.0mg/day) studies (4–32 weeks). Changes in metabolic parameters in adolescents were compared with those of olanzapine-treated adults (pooled from 84 clinical trials); changes in weight and BMI were compared with US age- and sex-adjusted standardized growth curves.

Results:

Olanzapine-treated adolescents had significant increases from baseline-to-endpoint in fasting glucose (p=.021); total cholesterol, LDL, and triglycerides (p<.001); and significant decreases in HDL (p<.001). Significantly more adolescents gained >=7% of their baseline weight versus adults (65.1% vs. 35.6%, p<.001); mean change from baseline-to-endpoint in weight was significantly greater in adolescents (7.0 vs. 3.3kg, p<.001). Adolescents had significantly lower mean changes from baseline-to-endpoint in fasting glucose (0.3 vs. 0.1mmol/L, p=.002) and triglycerides (0.3 vs. 0.2mmol/L, p=.007) versus adults. Significantly more adults experienced treatment-emergent normal-to-high changes at anytime in fasting glucose (4.8% vs. 1.2%, p=.033), total cholesterol (6.9% vs. 1.1%, p=.001), LDL (5.8% vs. 1.5%, p=.014), and triglycerides (25.7% vs. 17.4%, p=.030). Compared with standardized growth curves, olanzapine-treated adolescents had greater increases from baseline-to-endpoint in weight (1.0 vs. 7.1kg, p<.001), height (0.5 vs. 0.7cm, p<.001), and BMI (0.2 vs. 2.2kg/m2, p<.001).

Conclusion:

Olanzapine-treated adolescents may gain significantly more weight compared with adults, but may have smaller changes in other metabolic parameters. Clinicians may want to consider both efficacy and changes in metabolic parameters when selecting treatment options for individual adolescent patients.

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