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Over-Expression of Dopamine D(2) Receptor and Inwardly Rectifying Potassium Channel Genes in Drug-Naive Schizophrenic Peripheral Blood Lymphocytes as Potential Diagnostic Markers

Schizophrenia is one of the most common neuropsychiatric disorders affecting nearly 1% of the human population. Current diagnosis of schizophrenia is based on complex clinical symptoms. The use of easily detectable peripheral molecular markers could substantially help the diagnosis of psychiatric di...

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Autores principales: Zvara, Ágnes, Szekeres, György, Janka, Zoltán, Kelemen, János Z., Cimmer, Csongor, Sántha, Miklós, Puskás, László G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851074/
https://www.ncbi.nlm.nih.gov/pubmed/15920292
http://dx.doi.org/10.1155/2005/275318
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author Zvara, Ágnes
Szekeres, György
Janka, Zoltán
Kelemen, János Z.
Cimmer, Csongor
Sántha, Miklós
Puskás, László G.
author_facet Zvara, Ágnes
Szekeres, György
Janka, Zoltán
Kelemen, János Z.
Cimmer, Csongor
Sántha, Miklós
Puskás, László G.
author_sort Zvara, Ágnes
collection PubMed
description Schizophrenia is one of the most common neuropsychiatric disorders affecting nearly 1% of the human population. Current diagnosis of schizophrenia is based on complex clinical symptoms. The use of easily detectable peripheral molecular markers could substantially help the diagnosis of psychiatric disorders. Recent studies showed that peripheral blood lymphocytes (PBL) express subtypes of D1 and D2 subclasses of dopamine receptors. Recently, dopamine receptor D(3) (DRD3) was found to be over-expressed in schizophrenic PBL and proposed to be a diagnostic and follow-up marker for schizophrenia. In this study we screened PBL of 13 drug-naive/drug-free schizophrenic patients to identify additional markers of schizophrenia. One of the benefits of our study is the use of blood samples of non-medicated, drug-naive patients. This excludes the possibility that changes detected in gene expression levels might be attributed to the medication rather than to the disorder itself. Among others, genes for dopamine receptor D(2) (DRD2) and the inwardly rectifying potassium channel (Kir2.3) were found to be over-expressed in microarray analysis. Increased mRNA levels were confirmed by quantitative real-time PCR (QRT-PCR) using the SybrGreen method and dual labeled TaqMan probes. The use of both molecular markers allows a more rapid and precise prediction of schizophrenia and might help find the optimal medication for schizophrenic patients.
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spelling pubmed-38510742013-12-22 Over-Expression of Dopamine D(2) Receptor and Inwardly Rectifying Potassium Channel Genes in Drug-Naive Schizophrenic Peripheral Blood Lymphocytes as Potential Diagnostic Markers Zvara, Ágnes Szekeres, György Janka, Zoltán Kelemen, János Z. Cimmer, Csongor Sántha, Miklós Puskás, László G. Dis Markers Other Schizophrenia is one of the most common neuropsychiatric disorders affecting nearly 1% of the human population. Current diagnosis of schizophrenia is based on complex clinical symptoms. The use of easily detectable peripheral molecular markers could substantially help the diagnosis of psychiatric disorders. Recent studies showed that peripheral blood lymphocytes (PBL) express subtypes of D1 and D2 subclasses of dopamine receptors. Recently, dopamine receptor D(3) (DRD3) was found to be over-expressed in schizophrenic PBL and proposed to be a diagnostic and follow-up marker for schizophrenia. In this study we screened PBL of 13 drug-naive/drug-free schizophrenic patients to identify additional markers of schizophrenia. One of the benefits of our study is the use of blood samples of non-medicated, drug-naive patients. This excludes the possibility that changes detected in gene expression levels might be attributed to the medication rather than to the disorder itself. Among others, genes for dopamine receptor D(2) (DRD2) and the inwardly rectifying potassium channel (Kir2.3) were found to be over-expressed in microarray analysis. Increased mRNA levels were confirmed by quantitative real-time PCR (QRT-PCR) using the SybrGreen method and dual labeled TaqMan probes. The use of both molecular markers allows a more rapid and precise prediction of schizophrenia and might help find the optimal medication for schizophrenic patients. IOS Press 2005 2005-05-26 /pmc/articles/PMC3851074/ /pubmed/15920292 http://dx.doi.org/10.1155/2005/275318 Text en Copyright © 2005 Hindawi Publishing Corporation.
spellingShingle Other
Zvara, Ágnes
Szekeres, György
Janka, Zoltán
Kelemen, János Z.
Cimmer, Csongor
Sántha, Miklós
Puskás, László G.
Over-Expression of Dopamine D(2) Receptor and Inwardly Rectifying Potassium Channel Genes in Drug-Naive Schizophrenic Peripheral Blood Lymphocytes as Potential Diagnostic Markers
title Over-Expression of Dopamine D(2) Receptor and Inwardly Rectifying Potassium Channel Genes in Drug-Naive Schizophrenic Peripheral Blood Lymphocytes as Potential Diagnostic Markers
title_full Over-Expression of Dopamine D(2) Receptor and Inwardly Rectifying Potassium Channel Genes in Drug-Naive Schizophrenic Peripheral Blood Lymphocytes as Potential Diagnostic Markers
title_fullStr Over-Expression of Dopamine D(2) Receptor and Inwardly Rectifying Potassium Channel Genes in Drug-Naive Schizophrenic Peripheral Blood Lymphocytes as Potential Diagnostic Markers
title_full_unstemmed Over-Expression of Dopamine D(2) Receptor and Inwardly Rectifying Potassium Channel Genes in Drug-Naive Schizophrenic Peripheral Blood Lymphocytes as Potential Diagnostic Markers
title_short Over-Expression of Dopamine D(2) Receptor and Inwardly Rectifying Potassium Channel Genes in Drug-Naive Schizophrenic Peripheral Blood Lymphocytes as Potential Diagnostic Markers
title_sort over-expression of dopamine d(2) receptor and inwardly rectifying potassium channel genes in drug-naive schizophrenic peripheral blood lymphocytes as potential diagnostic markers
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851074/
https://www.ncbi.nlm.nih.gov/pubmed/15920292
http://dx.doi.org/10.1155/2005/275318
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