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Psychophysiological Markers of Vulnerability to Psychopathology in Men with an Extra X Chromosome (XXY)

Studying genetically defined syndromes associated with increased risk for psychopathology may help in understanding neurodevelopmental mechanisms related to risk for psychopathology. Klinefelter syndrome (47,XXY) is one of the most common sex chromosomal aneuploidies (1 in 650 male births) and assoc...

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Autores principales: van Rijn, Sophie, Swaab, Hanna, Magnée, Maurice, van Engeland, Herman, Kemner, Chantal
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105055/
https://www.ncbi.nlm.nih.gov/pubmed/21655260
http://dx.doi.org/10.1371/journal.pone.0020292
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author van Rijn, Sophie
Swaab, Hanna
Magnée, Maurice
van Engeland, Herman
Kemner, Chantal
author_facet van Rijn, Sophie
Swaab, Hanna
Magnée, Maurice
van Engeland, Herman
Kemner, Chantal
author_sort van Rijn, Sophie
collection PubMed
description Studying genetically defined syndromes associated with increased risk for psychopathology may help in understanding neurodevelopmental mechanisms related to risk for psychopathology. Klinefelter syndrome (47,XXY) is one of the most common sex chromosomal aneuploidies (1 in 650 male births) and associated with increased vulnerability for psychopathology, including psychotic symptoms. Yet, it remains unknown whether this increased risk is associated with underlying psychophysiological mechanisms that are typically deficient in individuals with psychotic disorders. The present study assessed three “classic” psychophysiological markers of psychosis in Klinefelter syndrome (KS): smooth pursuit eye movements (SPEM), prepulse inhibition (PPI) and P50 suppression. Fourteen adults with KS and 15 non-clinical adults participated in the study. Data on SPEM (reflecting visuo-motor control) as well as PPI and P50 suppression (reflecting sensory gating) were collected. Dysfunctions in SPEM were observed in individuals with KS, with less smooth pursuit as expressed in lower position gain. Also, reduced sensory gating in individuals with KS was suggested by significantly reduced prepulse inhibition of the startle response (PPI) (effect size 1.6). No abnormalities were found in suppression of the P50 (effect size 0.6). We speculate that impairments in these psychophysiological mechanisms may reflect core brain dysfunctions that may also mediate the described increased vulnerability for psychotic symptoms in KS. Although speculative, such deficit specific, rather than disorder specific, psychophysiological dysfunctions in KS might convey vulnerability to other types of psychopathology as well. As KS already can be diagnosed prenatally, the predictive value of childhood impairments in prepulse inhibition and smooth pursuit for development of psychopathology later in life could be assessed. In sum, studying individuals with KS may prove to be an avenue of research leading to new hypotheses and insights into “at risk” pathways to psychopathology.
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spelling pubmed-31050552011-06-08 Psychophysiological Markers of Vulnerability to Psychopathology in Men with an Extra X Chromosome (XXY) van Rijn, Sophie Swaab, Hanna Magnée, Maurice van Engeland, Herman Kemner, Chantal PLoS One Research Article Studying genetically defined syndromes associated with increased risk for psychopathology may help in understanding neurodevelopmental mechanisms related to risk for psychopathology. Klinefelter syndrome (47,XXY) is one of the most common sex chromosomal aneuploidies (1 in 650 male births) and associated with increased vulnerability for psychopathology, including psychotic symptoms. Yet, it remains unknown whether this increased risk is associated with underlying psychophysiological mechanisms that are typically deficient in individuals with psychotic disorders. The present study assessed three “classic” psychophysiological markers of psychosis in Klinefelter syndrome (KS): smooth pursuit eye movements (SPEM), prepulse inhibition (PPI) and P50 suppression. Fourteen adults with KS and 15 non-clinical adults participated in the study. Data on SPEM (reflecting visuo-motor control) as well as PPI and P50 suppression (reflecting sensory gating) were collected. Dysfunctions in SPEM were observed in individuals with KS, with less smooth pursuit as expressed in lower position gain. Also, reduced sensory gating in individuals with KS was suggested by significantly reduced prepulse inhibition of the startle response (PPI) (effect size 1.6). No abnormalities were found in suppression of the P50 (effect size 0.6). We speculate that impairments in these psychophysiological mechanisms may reflect core brain dysfunctions that may also mediate the described increased vulnerability for psychotic symptoms in KS. Although speculative, such deficit specific, rather than disorder specific, psychophysiological dysfunctions in KS might convey vulnerability to other types of psychopathology as well. As KS already can be diagnosed prenatally, the predictive value of childhood impairments in prepulse inhibition and smooth pursuit for development of psychopathology later in life could be assessed. In sum, studying individuals with KS may prove to be an avenue of research leading to new hypotheses and insights into “at risk” pathways to psychopathology. Public Library of Science 2011-05-31 /pmc/articles/PMC3105055/ /pubmed/21655260 http://dx.doi.org/10.1371/journal.pone.0020292 Text en van Rijn et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
van Rijn, Sophie
Swaab, Hanna
Magnée, Maurice
van Engeland, Herman
Kemner, Chantal
Psychophysiological Markers of Vulnerability to Psychopathology in Men with an Extra X Chromosome (XXY)
title Psychophysiological Markers of Vulnerability to Psychopathology in Men with an Extra X Chromosome (XXY)
title_full Psychophysiological Markers of Vulnerability to Psychopathology in Men with an Extra X Chromosome (XXY)
title_fullStr Psychophysiological Markers of Vulnerability to Psychopathology in Men with an Extra X Chromosome (XXY)
title_full_unstemmed Psychophysiological Markers of Vulnerability to Psychopathology in Men with an Extra X Chromosome (XXY)
title_short Psychophysiological Markers of Vulnerability to Psychopathology in Men with an Extra X Chromosome (XXY)
title_sort psychophysiological markers of vulnerability to psychopathology in men with an extra x chromosome (xxy)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105055/
https://www.ncbi.nlm.nih.gov/pubmed/21655260
http://dx.doi.org/10.1371/journal.pone.0020292
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