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Whole genome methylation analyses of schizophrenia patients before and after treatment

The aetiology of schizophrenia is still unknown but it involves both heritable and non-heritable factors. DNA methylation is an inheritable epigenetic modification that stably alters gene expression. It takes part in the regulation of neurodevelopment and may be a contributing factor to the pathogen...

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Autores principales: Rukova, Blaga, Staneva, Rada, Hadjidekova, Savina, Stamenov, Georgi, Milanova, Vihra, Toncheva, Draga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434134/
https://www.ncbi.nlm.nih.gov/pubmed/26019538
http://dx.doi.org/10.1080/13102818.2014.933501
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author Rukova, Blaga
Staneva, Rada
Hadjidekova, Savina
Stamenov, Georgi
Milanova, Vihra
Toncheva, Draga
author_facet Rukova, Blaga
Staneva, Rada
Hadjidekova, Savina
Stamenov, Georgi
Milanova, Vihra
Toncheva, Draga
author_sort Rukova, Blaga
collection PubMed
description The aetiology of schizophrenia is still unknown but it involves both heritable and non-heritable factors. DNA methylation is an inheritable epigenetic modification that stably alters gene expression. It takes part in the regulation of neurodevelopment and may be a contributing factor to the pathogenesis of brain diseases. It was found that many of the antipsychotic drugs may lead to epigenetic modifications. We have performed 42 high-resolution genome-wide methylation array analyses to determine the methylation status of 27,627 CpG islands. Differentially methylated regions were studied with samples from 20 Bulgarian individuals divided in four groups according to their gender (12 males/8 females) and their treatment response (6 in complete/14 in incomplete remission). They were compared to two age and sex matched control pools (110 females in female pool/110 males in male pool) before and after treatment. We found significant differences in the methylation profiles between male schizophrenia patients with complete remission and control male pool before treatment (C16orf70, CST3, DDRGK1, FA2H, FLJ30058, MFSD2B, RFX4, UBE2J1, ZNF311) and male schizophrenia patients with complete remission and control male pool after treatment (AP1S3, C16orf59, KCNK15, LOC146336, MGC16384, XRN2) that potentially could be used as target genes for new therapeutic strategies as well as markers for good treatment response. Our data revealed major differences in methylation profiles between male schizophrenia patients in complete remission before and after treatment and healthy controls which supports the hypothesis that antipsychotic drugs may play a role in epigenetic modifications.
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spelling pubmed-44341342015-05-25 Whole genome methylation analyses of schizophrenia patients before and after treatment Rukova, Blaga Staneva, Rada Hadjidekova, Savina Stamenov, Georgi Milanova, Vihra Toncheva, Draga Biotechnol Biotechnol Equip Articles; Medical Biotechnology The aetiology of schizophrenia is still unknown but it involves both heritable and non-heritable factors. DNA methylation is an inheritable epigenetic modification that stably alters gene expression. It takes part in the regulation of neurodevelopment and may be a contributing factor to the pathogenesis of brain diseases. It was found that many of the antipsychotic drugs may lead to epigenetic modifications. We have performed 42 high-resolution genome-wide methylation array analyses to determine the methylation status of 27,627 CpG islands. Differentially methylated regions were studied with samples from 20 Bulgarian individuals divided in four groups according to their gender (12 males/8 females) and their treatment response (6 in complete/14 in incomplete remission). They were compared to two age and sex matched control pools (110 females in female pool/110 males in male pool) before and after treatment. We found significant differences in the methylation profiles between male schizophrenia patients with complete remission and control male pool before treatment (C16orf70, CST3, DDRGK1, FA2H, FLJ30058, MFSD2B, RFX4, UBE2J1, ZNF311) and male schizophrenia patients with complete remission and control male pool after treatment (AP1S3, C16orf59, KCNK15, LOC146336, MGC16384, XRN2) that potentially could be used as target genes for new therapeutic strategies as well as markers for good treatment response. Our data revealed major differences in methylation profiles between male schizophrenia patients in complete remission before and after treatment and healthy controls which supports the hypothesis that antipsychotic drugs may play a role in epigenetic modifications. Taylor & Francis 2014-05-04 2014-08-26 /pmc/articles/PMC4434134/ /pubmed/26019538 http://dx.doi.org/10.1080/13102818.2014.933501 Text en © 2014 The Author(s). Published by Taylor & Francis. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Articles; Medical Biotechnology
Rukova, Blaga
Staneva, Rada
Hadjidekova, Savina
Stamenov, Georgi
Milanova, Vihra
Toncheva, Draga
Whole genome methylation analyses of schizophrenia patients before and after treatment
title Whole genome methylation analyses of schizophrenia patients before and after treatment
title_full Whole genome methylation analyses of schizophrenia patients before and after treatment
title_fullStr Whole genome methylation analyses of schizophrenia patients before and after treatment
title_full_unstemmed Whole genome methylation analyses of schizophrenia patients before and after treatment
title_short Whole genome methylation analyses of schizophrenia patients before and after treatment
title_sort whole genome methylation analyses of schizophrenia patients before and after treatment
topic Articles; Medical Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434134/
https://www.ncbi.nlm.nih.gov/pubmed/26019538
http://dx.doi.org/10.1080/13102818.2014.933501
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