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EPA-1506 – Impact of Brain-derived Neurotrophic Factor (BDNF) Gene Polymorphism on Cortical Inhibition in Schizophrenia

Published online by Cambridge University Press:  15 April 2020

W. Strube
Affiliation:
Psychiatry, Klinikum der LMU München, Munich, Germany
T. Bunse
Affiliation:
Psychiatry, Klinikum der LMU München, Munich, Germany
T. Wobrock
Affiliation:
Psychiatry, Georg-August-University, Göttingen, Germany
S. Witt
Affiliation:
Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Mannheim, Germany
V. Nieratschker
Affiliation:
Molecular Psychiatry, University Tübingen, Tübingen, Germany
P. Falkai
Affiliation:
Psychiatry, Klinikum der LMU München, Munich, Germany
A. Hasan
Affiliation:
Psychiatry, Klinikum der LMU München, Munich, Germany

Abstract

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Introduction

Neuronal plasticity is a characteristic feature of the human central nervous system. Impaired cortical plasticity has been reported to be associated with a val/met gene-polymorphism in the brain-derived neurotrophic factor (BDNF) gene. Based on former studies, impaired cortical plasticity has been described as a common, yet not fully understood phenomenon in patients with schizophrenia.

Objectives

The aim of the study was to investigate the impact of the val/met-BDNF gene-polymorphism on cortical plasticity in patients with schizophrenia.

Materials & Methods

Cortical plasticity was investigated in a cross-sectional sample of schizophrenia patients (SZ) and healthy controls (HC) using anodal and cathodal transcranial direct current stimulation (tDCS) applied to the primary motor cortex inducing long-term potentiation (LTP) and depression (LTD). The after-effect of the applied tDCS was then probed by TMS before and after tDCS stimulation. TMS in all participants was conducted using a standard 70 mm-TMS figure-of-eight magnetic coil connected to a MagPro X 100 magnetic stimulator. Analyses were focused on resting-motor threshold (RMT), 1mV motor-evoked potential (MEP), short-interval intracortical inhibition (SICI at 3 ms), intracortical facilitation (ICF at 12 ms) and cortical silent period (CSP at 120% RMT).

Results

The statistical analyses included n=43 SZ and n=44 HC participants (all numbers presented under reserve of further examination) thus resulting in the largest available sample to probe cortical plasticity parameters in BDNF-genotyped schizophrenia patients. Further results will be presented at the conference.

Conclusion

The findings will give new insights into the influence of plasticity-associated gene polymorphisms and the pathophysiology of schizophrenia.

Type
P31 - Schizophrenia
Copyright
Copyright © European Psychiatric Association 2014
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