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Brain structure, cognition and negative symptoms in schizophrenia are associated with serum levels of polysialic acid-modified NCAM

The neural cell adhesion molecule (NCAM) is a glycoprotein implicated in cell–cell adhesion, neurite outgrowth and synaptic plasticity. Polysialic acid (polySia) is mainly attached to NCAM (polySia-NCAM) and has an essential role in regulating NCAM-dependent developmental processes that require plas...

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Autores principales: Piras, F, Schiff, M, Chiapponi, C, Bossù, P, Mühlenhoff, M, Caltagirone, C, Gerardy-Schahn, R, Hildebrandt, H, Spalletta, G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930132/
https://www.ncbi.nlm.nih.gov/pubmed/26460482
http://dx.doi.org/10.1038/tp.2015.156
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author Piras, F
Schiff, M
Chiapponi, C
Bossù, P
Mühlenhoff, M
Caltagirone, C
Gerardy-Schahn, R
Hildebrandt, H
Spalletta, G
author_facet Piras, F
Schiff, M
Chiapponi, C
Bossù, P
Mühlenhoff, M
Caltagirone, C
Gerardy-Schahn, R
Hildebrandt, H
Spalletta, G
author_sort Piras, F
collection PubMed
description The neural cell adhesion molecule (NCAM) is a glycoprotein implicated in cell–cell adhesion, neurite outgrowth and synaptic plasticity. Polysialic acid (polySia) is mainly attached to NCAM (polySia-NCAM) and has an essential role in regulating NCAM-dependent developmental processes that require plasticity, that is, cell migration, axon guidance and synapse formation. Post-mortem and genetic evidence suggests that dysregulation of polySia-NCAM is involved in schizophrenia (SZ). We enrolled 45 patients diagnosed with SZ and 45 healthy individuals who were submitted to polySia-NCAM peripheral quantification, cognitive and psychopathological assessment and structural neuroimaging (brain volumes and diffusion tensor imaging). PolySia-NCAM serum levels were increased in SZ patients, independently of antipsychotic treatment, and were associated with negative symptoms, blunted affect and declarative memory impairment. The increased polySia-NCAM levels were associated with decreased volume in the left prefrontal cortex, namely Brodmann area 46, in patients and increased volume in the same brain area of healthy individuals. As this brain region is involved in the pathophysiology of SZ and its associated phenomenology, the data indicate that polySia-NCAM deserves further scrutiny because of its possible role in early neurodevelopmental mechanisms of the disorder.
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spelling pubmed-49301322016-07-14 Brain structure, cognition and negative symptoms in schizophrenia are associated with serum levels of polysialic acid-modified NCAM Piras, F Schiff, M Chiapponi, C Bossù, P Mühlenhoff, M Caltagirone, C Gerardy-Schahn, R Hildebrandt, H Spalletta, G Transl Psychiatry Original Article The neural cell adhesion molecule (NCAM) is a glycoprotein implicated in cell–cell adhesion, neurite outgrowth and synaptic plasticity. Polysialic acid (polySia) is mainly attached to NCAM (polySia-NCAM) and has an essential role in regulating NCAM-dependent developmental processes that require plasticity, that is, cell migration, axon guidance and synapse formation. Post-mortem and genetic evidence suggests that dysregulation of polySia-NCAM is involved in schizophrenia (SZ). We enrolled 45 patients diagnosed with SZ and 45 healthy individuals who were submitted to polySia-NCAM peripheral quantification, cognitive and psychopathological assessment and structural neuroimaging (brain volumes and diffusion tensor imaging). PolySia-NCAM serum levels were increased in SZ patients, independently of antipsychotic treatment, and were associated with negative symptoms, blunted affect and declarative memory impairment. The increased polySia-NCAM levels were associated with decreased volume in the left prefrontal cortex, namely Brodmann area 46, in patients and increased volume in the same brain area of healthy individuals. As this brain region is involved in the pathophysiology of SZ and its associated phenomenology, the data indicate that polySia-NCAM deserves further scrutiny because of its possible role in early neurodevelopmental mechanisms of the disorder. Nature Publishing Group 2015-10 2015-10-13 /pmc/articles/PMC4930132/ /pubmed/26460482 http://dx.doi.org/10.1038/tp.2015.156 Text en Copyright © 2015 Macmillan Publishers Limited 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
Piras, F
Schiff, M
Chiapponi, C
Bossù, P
Mühlenhoff, M
Caltagirone, C
Gerardy-Schahn, R
Hildebrandt, H
Spalletta, G
Brain structure, cognition and negative symptoms in schizophrenia are associated with serum levels of polysialic acid-modified NCAM
title Brain structure, cognition and negative symptoms in schizophrenia are associated with serum levels of polysialic acid-modified NCAM
title_full Brain structure, cognition and negative symptoms in schizophrenia are associated with serum levels of polysialic acid-modified NCAM
title_fullStr Brain structure, cognition and negative symptoms in schizophrenia are associated with serum levels of polysialic acid-modified NCAM
title_full_unstemmed Brain structure, cognition and negative symptoms in schizophrenia are associated with serum levels of polysialic acid-modified NCAM
title_short Brain structure, cognition and negative symptoms in schizophrenia are associated with serum levels of polysialic acid-modified NCAM
title_sort brain structure, cognition and negative symptoms in schizophrenia are associated with serum levels of polysialic acid-modified ncam
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930132/
https://www.ncbi.nlm.nih.gov/pubmed/26460482
http://dx.doi.org/10.1038/tp.2015.156
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