Hostname: page-component-586b7cd67f-l7hp2 Total loading time: 0 Render date: 2024-11-29T03:01:17.359Z Has data issue: false hasContentIssue false

S28-03 - Pharmacogenetics of Therapy Response in Schizophrenia

Published online by Cambridge University Press:  17 April 2020

I. Spellmann
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
D. Rujescu
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
R. Musil
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
A. Mayr
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
I. Giegling
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
J. Genius
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
P. Zill
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
S. Dehning
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
A.M. Hartmann
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
B. Bondy
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
N. Müller
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
H.-J. Möller
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany
M. Riedel
Affiliation:
Ludwig-Maximilians University Munich, Munich, Germany

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Pharmacogenetics in schizophrenia comprises pharmacokinetical and pharmacodynamical aspects as well as an approach to identify candidate genes associated with therapy response or side effects. Firstly focussing on classical drug targets like dopaminergic or serotonergic receptors, currently also developmental and regulatory genes presumably associated with effects of antipsychotic therapy are identified. The aim of this study was to investigate associations between therapy response in schizophrenic patients and different polymorphisms previously been identified within a genome wide array in rodents treated with MK-801 and/or haloperidol combined with some well-known schizophrenia candidate genes. We genotyped for 200 different polymorphisms in 285 schizophrenic patients, who were treated with different antipsychotics within randomized controlled trials. Psychopathology was measured weekly using the PANSS scale. Correlations between psychopathology and genotypes were calculated by using a linear model (ANCOVA).

We found significant associations between some well-known candidate genes (e.g. D2-, 5HT1A-, and α1A-receptors) and different PANSS subscales at baseline and after four weeks of antipsychotic treatment considered as therapy response. Furthermore we also identified several significant associations between some genes introduced from the animal model and psychopathology at baseline and towards therapy response. Some of them were formerly described in the literature (e.g. Homer1, Phospholipase C and Transthyretin), but most of them have not been related to schizophrenia or antipsychotic treatment by now (e.g. PLEKHA6, CLIC6 and SOSTDC1).

This indicates an involvement of genes in the pathophysiology of schizophrenia apart from yet known candidate genes and might further help in detecting differential therapy response in individuals with schizophrenia.

Type
Pharmacogenetics of first and second generation antipsychotics – efficacy and tolerabilityc
Copyright
Copyright © European Psychiatric Association 2010
Submit a response

Comments

No Comments have been published for this article.