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The risk of metabolic disorders in patients treated with asenapine or olanzapine: a study conducted on real-world data in Italy and Spain.

Authors :
Maina G
Ripellino C
Source :
Expert opinion on drug safety [Expert Opin Drug Saf] 2014 Sep; Vol. 13 (9), pp. 1149-54. Date of Electronic Publication: 2014 Jul 18.
Publication Year :
2014

Abstract

Background: Atypical antipsychotics are the main treatment for a large number of psychiatric illnesses, with fewer extrapyramidal effects than conventional antipsychotics. However, it has been suggested that their use is associated with increased risk of dyslipidemia and type 2 diabetes mellitus.<br />Objective: The risk of metabolic adverse effects associated with asenapine was assessed in comparison with that associated with olanzapine using real-world data.<br />Methods: This study was a retrospective analysis based on data extracted from the Italian and Spanish Cegedim Strategic Data Longitudinal Patient-Data databases. Patients with asenapine or olanzapine prescriptions were retrieved from September 2010 to December 2012 using strict inclusion criteria to guarantee minimization of confounders. Patients with type 2 diabetes mellitus and dyslipidemia were identified by using ICD9 codes and by antidiabetic and dyslipidemic drug prescriptions. The presence or absence of the metabolic condition was compared before and after treatment, and between cohorts.<br />Results: The retrospective analysis showed a lower risk of developing type 2 diabetes with asenapine than with olanzapine (2.2 vs 3.5%, respectively; p value: 0.0002) and of developing dyslipidemia (2.8 vs 6.8%, respectively; p value: 0.0001).<br />Conclusions: Asenapine is associated with a lower risk of metabolic adverse effects than olanzapine, demonstrating its improved safety profile.

Details

Language :
English
ISSN :
1744-764X
Volume :
13
Issue :
9
Database :
MEDLINE
Journal :
Expert opinion on drug safety
Publication Type :
Academic Journal
Accession number :
25036458
Full Text :
https://doi.org/10.1517/14740338.2014.943732