Multivariate patterns of gray matter volume in thalamic nuclei are associated with positive schizotypy in healthy individuals.


Journal

Psychological medicine
ISSN: 1469-8978
Titre abrégé: Psychol Med
Pays: England
ID NLM: 1254142

Informations de publication

Date de publication:
07 2020
Historique:
pubmed: 31 7 2019
medline: 14 5 2021
entrez: 31 7 2019
Statut: ppublish

Résumé

Previous models suggest biological and behavioral continua among healthy individuals (HC), at-risk condition, and full-blown schizophrenia (SCZ). Part of these continua may be captured by schizotypy, which shares subclinical traits and biological phenotypes with SCZ, including thalamic structural abnormalities. In this regard, previous findings have suggested that multivariate volumetric patterns of individual thalamic nuclei discriminate HC from SCZ. These results were obtained using machine learning, which allows case-control classification at the single-subject level. However, machine learning accuracy is usually unsatisfactory possibly due to phenotype heterogeneity. Indeed, a source of misclassification may be related to thalamic structural characteristics of those HC with high schizotypy, which may resemble structural abnormalities of SCZ. We hypothesized that thalamic structural heterogeneity is related to schizotypy, such that high schizotypal burden would implicate misclassification of those HC whose thalamic patterns resemble SCZ abnormalities. Following a previous report, we used Random Forests to predict diagnosis in a case-control sample (SCZ = 131, HC = 255) based on thalamic nuclei gray matter volumes estimates. Then, we investigated whether the likelihood to be classified as SCZ (π-SCZ) was associated with schizotypy in 174 HC, evaluated with the Schizotypal Personality Questionnaire. Prediction accuracy was 72.5%. Misclassified HC had higher positive schizotypy scores, which were correlated with π-SCZ. Results were specific to thalamic rather than whole-brain structural features. These findings strengthen the relevance of thalamic structural abnormalities to SCZ and suggest that multivariate thalamic patterns are correlates of the continuum between schizotypy in HC and the full-blown disease.

Sections du résumé

BACKGROUND
Previous models suggest biological and behavioral continua among healthy individuals (HC), at-risk condition, and full-blown schizophrenia (SCZ). Part of these continua may be captured by schizotypy, which shares subclinical traits and biological phenotypes with SCZ, including thalamic structural abnormalities. In this regard, previous findings have suggested that multivariate volumetric patterns of individual thalamic nuclei discriminate HC from SCZ. These results were obtained using machine learning, which allows case-control classification at the single-subject level. However, machine learning accuracy is usually unsatisfactory possibly due to phenotype heterogeneity. Indeed, a source of misclassification may be related to thalamic structural characteristics of those HC with high schizotypy, which may resemble structural abnormalities of SCZ. We hypothesized that thalamic structural heterogeneity is related to schizotypy, such that high schizotypal burden would implicate misclassification of those HC whose thalamic patterns resemble SCZ abnormalities.
METHODS
Following a previous report, we used Random Forests to predict diagnosis in a case-control sample (SCZ = 131, HC = 255) based on thalamic nuclei gray matter volumes estimates. Then, we investigated whether the likelihood to be classified as SCZ (π-SCZ) was associated with schizotypy in 174 HC, evaluated with the Schizotypal Personality Questionnaire.
RESULTS
Prediction accuracy was 72.5%. Misclassified HC had higher positive schizotypy scores, which were correlated with π-SCZ. Results were specific to thalamic rather than whole-brain structural features.
CONCLUSIONS
These findings strengthen the relevance of thalamic structural abnormalities to SCZ and suggest that multivariate thalamic patterns are correlates of the continuum between schizotypy in HC and the full-blown disease.

Identifiants

pubmed: 31358071
pii: S0033291719001430
doi: 10.1017/S0033291719001430
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1501-1509

Auteurs

Pasquale Di Carlo (P)

Group of Psychiatric Neuroscience, Department of Basic Medical Science, Neuroscience, and Sense Organs - University of Bari Aldo Moro, Bari, Italy.
Lieber Institute for Brain Development, Johns Hopkins Medical Campus - Baltimore, MD, USA.

Giulio Pergola (G)

Group of Psychiatric Neuroscience, Department of Basic Medical Science, Neuroscience, and Sense Organs - University of Bari Aldo Moro, Bari, Italy.
Lieber Institute for Brain Development, Johns Hopkins Medical Campus - Baltimore, MD, USA.

Linda A Antonucci (LA)

Group of Psychiatric Neuroscience, Department of Basic Medical Science, Neuroscience, and Sense Organs - University of Bari Aldo Moro, Bari, Italy.
Department of Psychiatry and Psychotherapy - Ludwig-Maximilians University, Munich, Germany.

Aurora Bonvino (A)

Group of Psychiatric Neuroscience, Department of Basic Medical Science, Neuroscience, and Sense Organs - University of Bari Aldo Moro, Bari, Italy.
IRCCS 'Casa Sollievo della Sofferenza', San Giovanni Rotondo, Italy.

Marina Mancini (M)

Group of Psychiatric Neuroscience, Department of Basic Medical Science, Neuroscience, and Sense Organs - University of Bari Aldo Moro, Bari, Italy.

Tiziana Quarto (T)

Group of Psychiatric Neuroscience, Department of Basic Medical Science, Neuroscience, and Sense Organs - University of Bari Aldo Moro, Bari, Italy.

Antonio Rampino (A)

Group of Psychiatric Neuroscience, Department of Basic Medical Science, Neuroscience, and Sense Organs - University of Bari Aldo Moro, Bari, Italy.
Azienda Ospedaliero-Universitaria Consorziale Policlinico, Bari, Italy.

Teresa Popolizio (T)

IRCCS 'Casa Sollievo della Sofferenza', San Giovanni Rotondo, Italy.

Alessandro Bertolino (A)

Group of Psychiatric Neuroscience, Department of Basic Medical Science, Neuroscience, and Sense Organs - University of Bari Aldo Moro, Bari, Italy.
Azienda Ospedaliero-Universitaria Consorziale Policlinico, Bari, Italy.

Giuseppe Blasi (G)

Group of Psychiatric Neuroscience, Department of Basic Medical Science, Neuroscience, and Sense Organs - University of Bari Aldo Moro, Bari, Italy.
Azienda Ospedaliero-Universitaria Consorziale Policlinico, Bari, Italy.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH