Literature DB >> 31581175

Multivariate classification of schizophrenia and its familial risk based on load-dependent attentional control brain functional connectivity.

Linda A Antonucci1,2,3, Nora Penzel4,5, Giulio Pergola6,7, Lana Kambeitz-Ilankovic4,5, Dominic Dwyer4, Joseph Kambeitz5, Shalaila Siobhan Haas4,8, Roberta Passiatore6, Leonardo Fazio9, Grazia Caforio6, Peter Falkai4, Giuseppe Blasi6, Alessandro Bertolino6, Nikolaos Koutsouleris4.   

Abstract

Patients with schizophrenia (SCZ), as well as their unaffected siblings (SIB), show functional connectivity (FC) alterations during performance of tasks involving attention. As compared with SCZ, these alterations are present in SIB to a lesser extent and are more pronounced during high cognitive demand, thus possibly representing one of the pathways in which familial risk is translated into the SCZ phenotype. Our aim is to measure the separability of SCZ and SIB from healthy controls (HC) using attentional control-dependent FC patterns, and to test to which extent these patterns span a continuum of neurofunctional alterations between HC and SCZ. 65 SCZ with 65 age and gender-matched HC and 39 SIB with 39 matched HC underwent the Variable Attentional Control (VAC) task. Load-dependent connectivity matrices were generated according to correct responses in each VAC load. Classification performances of high, intermediate and low VAC load FC on HC-SCZ and HC-SIB cohorts were tested through machine learning techniques within a repeated nested cross-validation framework. HC-SCZ classification models were applied to the HC-SIB cohort, and vice-versa. A high load-related decreased FC pattern discriminated between HC and SCZ with 66.9% accuracy and with 57.7% accuracy between HC and SIB. A high load-related increased FC network separated SIB from HC (69.6% accuracy), but not SCZ from HC (48.5% accuracy). Our findings revealed signatures of attentional FC abnormalities shared by SCZ and SIB individuals. We also found evidence for potential, SIB-specific FC signature, which may point to compensatory neurofunctional mechanisms in persons at familial risk for schizophrenia.

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Year:  2019        PMID: 31581175      PMCID: PMC7021788          DOI: 10.1038/s41386-019-0532-3

Source DB:  PubMed          Journal:  Neuropsychopharmacology        ISSN: 0893-133X            Impact factor:   7.853


  72 in total

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