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Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium

Cognitive impairment is a key feature of schizophrenia (SZ) and determines functional outcome. Nonetheless, molecular signatures in neuronal tissues that associate with deficits are not well understood. We conducted nasal biopsy to obtain olfactory epithelium from patients with SZ and control subjec...

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Autores principales: Horiuchi, Y, Kondo, M A, Okada, K, Takayanagi, Y, Tanaka, T, Ho, T, Varvaris, M, Tajinda, K, Hiyama, H, Ni, K, Colantuoni, C, Schretlen, D, Cascella, N G, Pevsner, J, Ishizuka, K, Sawa, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315541/
https://www.ncbi.nlm.nih.gov/pubmed/27727244
http://dx.doi.org/10.1038/tp.2016.154
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author Horiuchi, Y
Kondo, M A
Okada, K
Takayanagi, Y
Tanaka, T
Ho, T
Varvaris, M
Tajinda, K
Hiyama, H
Ni, K
Colantuoni, C
Schretlen, D
Cascella, N G
Pevsner, J
Ishizuka, K
Sawa, A
author_facet Horiuchi, Y
Kondo, M A
Okada, K
Takayanagi, Y
Tanaka, T
Ho, T
Varvaris, M
Tajinda, K
Hiyama, H
Ni, K
Colantuoni, C
Schretlen, D
Cascella, N G
Pevsner, J
Ishizuka, K
Sawa, A
author_sort Horiuchi, Y
collection PubMed
description Cognitive impairment is a key feature of schizophrenia (SZ) and determines functional outcome. Nonetheless, molecular signatures in neuronal tissues that associate with deficits are not well understood. We conducted nasal biopsy to obtain olfactory epithelium from patients with SZ and control subjects. The neural layers from the biopsied epithelium were enriched by laser-captured microdissection. We then performed an unbiased microarray expression study and implemented a systematic neuropsychological assessment on the same participants. The differentially regulated genes in SZ were further filtered based on correlation with neuropsychological traits. This strategy identified the SMAD 5 gene, and real-time quantitative PCR analysis also supports downregulation of the SMAD pathway in SZ. The SMAD pathway has been important in multiple tissues, including the role for neurodevelopment and bone formation. Here the involvement of the pathway in adult brain function is suggested. This exploratory study establishes a strategy to better identify neuronal molecular signatures that are potentially associated with mental illness and cognitive deficits. We propose that the SMAD pathway may be a novel target in addressing cognitive deficit of SZ in future studies.
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spelling pubmed-53155412017-02-27 Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium Horiuchi, Y Kondo, M A Okada, K Takayanagi, Y Tanaka, T Ho, T Varvaris, M Tajinda, K Hiyama, H Ni, K Colantuoni, C Schretlen, D Cascella, N G Pevsner, J Ishizuka, K Sawa, A Transl Psychiatry Original Article Cognitive impairment is a key feature of schizophrenia (SZ) and determines functional outcome. Nonetheless, molecular signatures in neuronal tissues that associate with deficits are not well understood. We conducted nasal biopsy to obtain olfactory epithelium from patients with SZ and control subjects. The neural layers from the biopsied epithelium were enriched by laser-captured microdissection. We then performed an unbiased microarray expression study and implemented a systematic neuropsychological assessment on the same participants. The differentially regulated genes in SZ were further filtered based on correlation with neuropsychological traits. This strategy identified the SMAD 5 gene, and real-time quantitative PCR analysis also supports downregulation of the SMAD pathway in SZ. The SMAD pathway has been important in multiple tissues, including the role for neurodevelopment and bone formation. Here the involvement of the pathway in adult brain function is suggested. This exploratory study establishes a strategy to better identify neuronal molecular signatures that are potentially associated with mental illness and cognitive deficits. We propose that the SMAD pathway may be a novel target in addressing cognitive deficit of SZ in future studies. Nature Publishing Group 2016-10 2016-10-11 /pmc/articles/PMC5315541/ /pubmed/27727244 http://dx.doi.org/10.1038/tp.2016.154 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Horiuchi, Y
Kondo, M A
Okada, K
Takayanagi, Y
Tanaka, T
Ho, T
Varvaris, M
Tajinda, K
Hiyama, H
Ni, K
Colantuoni, C
Schretlen, D
Cascella, N G
Pevsner, J
Ishizuka, K
Sawa, A
Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium
title Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium
title_full Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium
title_fullStr Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium
title_full_unstemmed Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium
title_short Molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium
title_sort molecular signatures associated with cognitive deficits in schizophrenia: a study of biopsied olfactory neural epithelium
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315541/
https://www.ncbi.nlm.nih.gov/pubmed/27727244
http://dx.doi.org/10.1038/tp.2016.154
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