Fronto-Thalamic Structural Connectivity Associated With Schizotypy, a Psychosis Risk Phenotype, in Nonclinical Subjects

Schizotypy is a risk phenotype for the psychosis spectrum and pilot studies suggest a biological continuum underlying this phenotype across health and disease. It is unclear whether this biological continuum might include brain structural associations in networks altered in schizophrenia spectrum di...

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Published inSchizophrenia bulletin Vol. 51; no. Supplement_2; pp. S137 - S148
Main Authors Nenadić, Igor, Mosebach, Johannes, Schmitt, Simon, Meller, Tina, Stein, Frederike, Brosch, Katharina, Ringwald, Kai, Pfarr, Julia-Katharina, Meinert, Susanne, Lemke, Hannah, Waltemate, Lena, Thiel, Katharina, Opel, Nils, Repple, Jonathan, Grotegerd, Dominik, Steinsträter, Olaf, Sommer, Jens, Hahn, Tim, Jansen, Andreas, Dannlowski, Udo, Krug, Axel, Kircher, Tilo
Format Journal Article
LanguageEnglish
Published United States Oxford University Press 04.03.2025
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Abstract Schizotypy is a risk phenotype for the psychosis spectrum and pilot studies suggest a biological continuum underlying this phenotype across health and disease. It is unclear whether this biological continuum might include brain structural associations in networks altered in schizophrenia spectrum disorders, such as the fronto-thalamo-striatal system or nodes of the default mode network, such as the precuneus. In this study, we analyze a large multi-center cohort of 673 nonclinical subjects phenotyped for schizotypal traits (using the Schizotypal Personality Questionnaire-Brief version) using tract-based spatial statistics of diffusion tensor imaging data, as well as voxel-based morphometry (VBM) analysis of regional brain volumes and gyrification analysis of early neurodevelopmental markers of cortical folding on T1-weighted MRI. We identify significant (P < .05 family-wise error corrected) associations of schizotypy with major fiber tract fractional anisotropy: positive (cognitive-perceptual) schizotypy correlated negatively with the left anterior thalamic radiation (a principal thalamo-frontal projection), left uncinate fasciculus and cingulum, while negative (interpersonal) schizotypy correlated positively with left anterior thalamic radiation, cingulum, and the anterior corpus callosum, and disorganized schizotypy correlated negatively with right cingulum, and superior and inferior longitudinal fasciculi. VBM analyses showed a negative correlation of gray matter with negative schizotypy in the left cerebellum, while gyrification in the inferior parietal cortex correlated positively with negative (interpersonal) schizotypy. These findings pave the way for a neural network conceptualization of schizotypy as a psychosis proneness trait across the general population, showing associations with fronto-subcortical and frontotemporal systems as structural substrates of this risk phenotype.
AbstractList Schizotypy is a risk phenotype for the psychosis spectrum and pilot studies suggest a biological continuum underlying this phenotype across health and disease. It is unclear whether this biological continuum might include brain structural associations in networks altered in schizophrenia spectrum disorders, such as the fronto-thalamo-striatal system or nodes of the default mode network, such as the precuneus.BACKGROUND AND HYPOTHESISSchizotypy is a risk phenotype for the psychosis spectrum and pilot studies suggest a biological continuum underlying this phenotype across health and disease. It is unclear whether this biological continuum might include brain structural associations in networks altered in schizophrenia spectrum disorders, such as the fronto-thalamo-striatal system or nodes of the default mode network, such as the precuneus.In this study, we analyze a large multi-center cohort of 673 nonclinical subjects phenotyped for schizotypal traits (using the Schizotypal Personality Questionnaire-Brief version) using tract-based spatial statistics of diffusion tensor imaging data, as well as voxel-based morphometry (VBM) analysis of regional brain volumes and gyrification analysis of early neurodevelopmental markers of cortical folding on T1-weighted MRI.STUDY DESIGNIn this study, we analyze a large multi-center cohort of 673 nonclinical subjects phenotyped for schizotypal traits (using the Schizotypal Personality Questionnaire-Brief version) using tract-based spatial statistics of diffusion tensor imaging data, as well as voxel-based morphometry (VBM) analysis of regional brain volumes and gyrification analysis of early neurodevelopmental markers of cortical folding on T1-weighted MRI.We identify significant (P < .05 family-wise error corrected) associations of schizotypy with major fiber tract fractional anisotropy: positive (cognitive-perceptual) schizotypy correlated negatively with the left anterior thalamic radiation (a principal thalamo-frontal projection), left uncinate fasciculus and cingulum, while negative (interpersonal) schizotypy correlated positively with left anterior thalamic radiation, cingulum, and the anterior corpus callosum, and disorganized schizotypy correlated negatively with right cingulum, and superior and inferior longitudinal fasciculi. VBM analyses showed a negative correlation of gray matter with negative schizotypy in the left cerebellum, while gyrification in the inferior parietal cortex correlated positively with negative (interpersonal) schizotypy.STUDY RESULTSWe identify significant (P < .05 family-wise error corrected) associations of schizotypy with major fiber tract fractional anisotropy: positive (cognitive-perceptual) schizotypy correlated negatively with the left anterior thalamic radiation (a principal thalamo-frontal projection), left uncinate fasciculus and cingulum, while negative (interpersonal) schizotypy correlated positively with left anterior thalamic radiation, cingulum, and the anterior corpus callosum, and disorganized schizotypy correlated negatively with right cingulum, and superior and inferior longitudinal fasciculi. VBM analyses showed a negative correlation of gray matter with negative schizotypy in the left cerebellum, while gyrification in the inferior parietal cortex correlated positively with negative (interpersonal) schizotypy.These findings pave the way for a neural network conceptualization of schizotypy as a psychosis proneness trait across the general population, showing associations with fronto-subcortical and frontotemporal systems as structural substrates of this risk phenotype.CONCLUSIONSThese findings pave the way for a neural network conceptualization of schizotypy as a psychosis proneness trait across the general population, showing associations with fronto-subcortical and frontotemporal systems as structural substrates of this risk phenotype.
Schizotypy is a risk phenotype for the psychosis spectrum and pilot studies suggest a biological continuum underlying this phenotype across health and disease. It is unclear whether this biological continuum might include brain structural associations in networks altered in schizophrenia spectrum disorders, such as the fronto-thalamo-striatal system or nodes of the default mode network, such as the precuneus. In this study, we analyze a large multi-center cohort of 673 nonclinical subjects phenotyped for schizotypal traits (using the Schizotypal Personality Questionnaire-Brief version) using tract-based spatial statistics of diffusion tensor imaging data, as well as voxel-based morphometry (VBM) analysis of regional brain volumes and gyrification analysis of early neurodevelopmental markers of cortical folding on T1-weighted MRI. We identify significant (P < .05 family-wise error corrected) associations of schizotypy with major fiber tract fractional anisotropy: positive (cognitive-perceptual) schizotypy correlated negatively with the left anterior thalamic radiation (a principal thalamo-frontal projection), left uncinate fasciculus and cingulum, while negative (interpersonal) schizotypy correlated positively with left anterior thalamic radiation, cingulum, and the anterior corpus callosum, and disorganized schizotypy correlated negatively with right cingulum, and superior and inferior longitudinal fasciculi. VBM analyses showed a negative correlation of gray matter with negative schizotypy in the left cerebellum, while gyrification in the inferior parietal cortex correlated positively with negative (interpersonal) schizotypy. These findings pave the way for a neural network conceptualization of schizotypy as a psychosis proneness trait across the general population, showing associations with fronto-subcortical and frontotemporal systems as structural substrates of this risk phenotype.
Author Meller, Tina
Jansen, Andreas
Ringwald, Kai
Pfarr, Julia-Katharina
Krug, Axel
Stein, Frederike
Steinsträter, Olaf
Hahn, Tim
Opel, Nils
Lemke, Hannah
Repple, Jonathan
Dannlowski, Udo
Meinert, Susanne
Schmitt, Simon
Grotegerd, Dominik
Brosch, Katharina
Mosebach, Johannes
Kircher, Tilo
Thiel, Katharina
Nenadić, Igor
Waltemate, Lena
Sommer, Jens
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Keywords magnetic resonance imaging (MRI)
psychosis proneness
gyrification
cortical folding
Language English
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Present address: Department of Psychiatry and Psychotherapy, MH Hannover, Hannover, Germany
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Snippet Schizotypy is a risk phenotype for the psychosis spectrum and pilot studies suggest a biological continuum underlying this phenotype across health and disease....
SourceID pubmedcentral
proquest
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
StartPage S137
SubjectTerms Adolescent
Adult
Cohort Studies
Connectome
Diffusion Tensor Imaging
Female
Frontal Lobe - diagnostic imaging
Frontal Lobe - pathology
Humans
Male
Nerve Net - diagnostic imaging
Nerve Net - pathology
Phenotype
Psychotic Disorders - pathology
Psychotic Disorders - physiopathology
Schizotypal Personality Disorder - diagnostic imaging
Schizotypal Personality Disorder - pathology
Schizotypal Personality Disorder - physiopathology
Supplement
Thalamus - diagnostic imaging
Thalamus - pathology
White Matter - diagnostic imaging
White Matter - pathology
Young Adult
Title Fronto-Thalamic Structural Connectivity Associated With Schizotypy, a Psychosis Risk Phenotype, in Nonclinical Subjects
URI https://www.ncbi.nlm.nih.gov/pubmed/40037831
https://www.proquest.com/docview/3174098621
https://pubmed.ncbi.nlm.nih.gov/PMC11879573
Volume 51
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