Back to Search Start Over

A preliminary study on methylphenidate-regulated gene expression in lymphoblastoid cells of ADHD patients

Authors :
Claus-J Ü Rgen Scholz
Sarah Kittel-Schneider
Heike Weber
Andreas Reif
Julia Heupel
Christian Jacob
Lena Weissflog
M. Hilscher
R. Schwarz
Brigitte Schmidt
Julia Volkert
Klaus-Peter Lesch
Susanne Reichert
Juliane Kopf
Psychiatrie & Neuropsychologie
RS: MHeNs - R3 - Neuroscience
Source :
ResearcherID, World Journal of Biological Psychiatry, 16(3), 180-9. Routledge/Taylor & Francis Group

Abstract

Objectives. Methylphenidate (MPH) is a commonly used stimulant medication for treating attention-deficit/hyperactivity disorder (ADHD). Besides inhibiting monoamine reuptake there is evidence that MPH also influences gene expression directly. Methods. We investigated the impact of MPH treatment on gene expression levels of lymphoblastoid cells derived from adult ADHD patients and healthy controls by hypothesis-free, genome-wide microarray analysis. Significant findings were subsequently confirmed by quantitative Real-Time PCR (qRT PCR) analysis. Results. The microarray analysis from pooled samples after correction for multiple testing revealed 138 genes to be marginally significantly regulated due to MPH treatment, and one gene due to diagnosis. By qRT PCR we could confirm that GUCY1B3 expression was differential due to diagnosis. We verified chronic MPH treatment effects on the expression of ATXN1, HEY1, MAP3K8 and GLUT3 in controls as well as acute treatment effects on the expression of NAV2 and ATXN1 specifically in ADHD patients. Conclusions. Our preliminary results demonstrate MPH treatment differences in ADHD patients and healthy controls in a peripheral primary cell model. Our results need to be replicated in larger samples and also using patient-derived neuronal cell models to validate the contribution of those genes to the pathophysiology of ADHD and mode of action of MPH.

Details

ISSN :
15622975
Database :
OpenAIRE
Journal :
ResearcherID, World Journal of Biological Psychiatry, 16(3), 180-9. Routledge/Taylor & Francis Group
Accession number :
edsair.doi.dedup.....dd271edaada10dcc1dff7212adf756fa