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Contribution of neurological soft signs’ studies to the understanding of the pathophysiology of schizophrenia

INTRODUCTION: Neurological soft signs (NSS) have long been described in schizophrenic patients. However, recent studies focusing on first-episode psychosis and at-risk mental states have brought up some aspects that may point to a neurodevelopmental underpinning of the disease. OBJECTIVES: We aimed...

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Autores principales: Reynolds De Sousa, T., André, R., Novais, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478875/
http://dx.doi.org/10.1192/j.eurpsy.2023.2315
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author Reynolds De Sousa, T.
André, R.
Novais, F.
author_facet Reynolds De Sousa, T.
André, R.
Novais, F.
author_sort Reynolds De Sousa, T.
collection PubMed
description INTRODUCTION: Neurological soft signs (NSS) have long been described in schizophrenic patients. However, recent studies focusing on first-episode psychosis and at-risk mental states have brought up some aspects that may point to a neurodevelopmental underpinning of the disease. OBJECTIVES: We aimed to review the published literature concerning NSS and psychosis and critically analyze it in regard to how it may constitute a body of evidence favouring the neurodevelopmental hypothesis of schizophrenia. METHODS: We conducted a Pubmed ® research using the following terms “neurological soft signs”, “psychosis”, “psychotic” and “first-episode”. RESULTS: The studies that have been carried out found a gradation of NSS scores that had its minimum values in healthy controls, intermediate scores in at-risk mental state individuals, and highest scores in first-episode psychosis. NSS correlate with various brain imaging anomalies, which indicates abnormal neurological function. Its scores also correlate with poorer cognitive performance and more prominent negative symptoms in the short- and long-term. Interestingly, patients who have psychotic episodes associated with cannabis use have lower NSS scores than all the other psychotic-illness diagnostic groups. CONCLUSIONS: NSS might thus translate a neurological dysfunction that exists previous to the psychotic break and is a measure of one’s vulnerability to psychosis. These results point to the existence of two distinct groups: one that has high NSS scores and therefore a high genetic vulnerability, needing little contribution of environmental factors to manifest a psychotic episode; and another one with low NSS scores, a smaller genetic vulnerability and a greater role played by environmental influences. DISCLOSURE OF INTEREST: None Declared
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spelling pubmed-104788752023-09-06 Contribution of neurological soft signs’ studies to the understanding of the pathophysiology of schizophrenia Reynolds De Sousa, T. André, R. Novais, F. Eur Psychiatry Abstract INTRODUCTION: Neurological soft signs (NSS) have long been described in schizophrenic patients. However, recent studies focusing on first-episode psychosis and at-risk mental states have brought up some aspects that may point to a neurodevelopmental underpinning of the disease. OBJECTIVES: We aimed to review the published literature concerning NSS and psychosis and critically analyze it in regard to how it may constitute a body of evidence favouring the neurodevelopmental hypothesis of schizophrenia. METHODS: We conducted a Pubmed ® research using the following terms “neurological soft signs”, “psychosis”, “psychotic” and “first-episode”. RESULTS: The studies that have been carried out found a gradation of NSS scores that had its minimum values in healthy controls, intermediate scores in at-risk mental state individuals, and highest scores in first-episode psychosis. NSS correlate with various brain imaging anomalies, which indicates abnormal neurological function. Its scores also correlate with poorer cognitive performance and more prominent negative symptoms in the short- and long-term. Interestingly, patients who have psychotic episodes associated with cannabis use have lower NSS scores than all the other psychotic-illness diagnostic groups. CONCLUSIONS: NSS might thus translate a neurological dysfunction that exists previous to the psychotic break and is a measure of one’s vulnerability to psychosis. These results point to the existence of two distinct groups: one that has high NSS scores and therefore a high genetic vulnerability, needing little contribution of environmental factors to manifest a psychotic episode; and another one with low NSS scores, a smaller genetic vulnerability and a greater role played by environmental influences. DISCLOSURE OF INTEREST: None Declared Cambridge University Press 2023-07-19 /pmc/articles/PMC10478875/ http://dx.doi.org/10.1192/j.eurpsy.2023.2315 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Reynolds De Sousa, T.
André, R.
Novais, F.
Contribution of neurological soft signs’ studies to the understanding of the pathophysiology of schizophrenia
title Contribution of neurological soft signs’ studies to the understanding of the pathophysiology of schizophrenia
title_full Contribution of neurological soft signs’ studies to the understanding of the pathophysiology of schizophrenia
title_fullStr Contribution of neurological soft signs’ studies to the understanding of the pathophysiology of schizophrenia
title_full_unstemmed Contribution of neurological soft signs’ studies to the understanding of the pathophysiology of schizophrenia
title_short Contribution of neurological soft signs’ studies to the understanding of the pathophysiology of schizophrenia
title_sort contribution of neurological soft signs’ studies to the understanding of the pathophysiology of schizophrenia
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478875/
http://dx.doi.org/10.1192/j.eurpsy.2023.2315
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