» Articles » PMID: 31507256

Predicting Psychosis Risk Using a Specific Measure of Cognitive Control: a 12-month Longitudinal Study

Overview
Journal Psychol Med
Specialty Psychology
Date 2019 Sep 12
PMID 31507256
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Identifying risk factors of individuals in a clinical-high-risk state for psychosis are vital to prevention and early intervention efforts. Among prodromal abnormalities, cognitive functioning has shown intermediate levels of impairment in CHR relative to first-episode psychosis and healthy controls, highlighting a potential role as a risk factor for transition to psychosis and other negative clinical outcomes. The current study used the AX-CPT, a brief 15-min computerized task, to determine whether cognitive control impairments in CHR at baseline could predict clinical status at 12-month follow-up.

Methods: Baseline AX-CPT data were obtained from 117 CHR individuals participating in two studies, the Early Detection, Intervention, and Prevention of Psychosis Program (EDIPPP) and the Understanding Early Psychosis Programs (EP) and used to predict clinical status at 12-month follow-up. At 12 months, 19 individuals converted to a first episode of psychosis (CHR-C), 52 remitted (CHR-R), and 46 had persistent sub-threshold symptoms (CHR-P). Binary logistic regression and multinomial logistic regression were used to test prediction models.

Results: Baseline AX-CPT performance (d-prime context) was less impaired in CHR-R compared to CHR-P and CHR-C patient groups. AX-CPT predictive validity was robust (0.723) for discriminating converters v. non-converters, and even greater (0.771) when predicting CHR three subgroups.

Conclusions: These longitudinal outcome data indicate that cognitive control deficits as measured by AX-CPT d-prime context are a strong predictor of clinical outcome in CHR individuals. The AX-CPT is brief, easily implemented and cost-effective measure that may be valuable for large-scale prediction efforts.

Citing Articles

Altered neural signalling during reward anticipation in children and early adolescents with high psychotic-like experiences.

Sen P, Knolle F Neuroimage Clin. 2025; 45:103756.

PMID: 39983553 PMC: 11889563. DOI: 10.1016/j.nicl.2025.103756.


Structural and functional connectivity in relation to executive functions in antipsychotic-naïve patients with first episode schizophrenia and levels of glutamatergic metabolites.

Kristensen T, Ambrosen K, Raghava J, Syeda W, Dhollander T, Lemvigh C Schizophrenia (Heidelb). 2024; 10(1):72.

PMID: 39217180 PMC: 11366027. DOI: 10.1038/s41537-024-00487-9.


Prefrontal Oscillatory Slowing in Early-Course Schizophrenia Is Associated With Worse Cognitive Performance and Negative Symptoms: A Transcranial Magnetic Stimulation-Electroencephalography Study.

Donati F, Mayeli A, Nascimento Couto B, Sharma K, Janssen S, Krafty R Biol Psychiatry Cogn Neurosci Neuroimaging. 2024; 10(2):158-166.

PMID: 39059465 PMC: 11759720. DOI: 10.1016/j.bpsc.2024.07.013.


Cognitive complaint inversely associated to UHR transition.

Hamdan-Dumont M, Lecardeur L, Habert M, Couturas J, Okassa M, Lacroix A Schizophr Res Cogn. 2024; 38:100319.

PMID: 39022601 PMC: 11253140. DOI: 10.1016/j.scog.2024.100319.


Longitudinal changes in neural gain and its relationship to cognitive control trajectory in young adults with early psychosis.

Burgher B, Scott J, Cocchi L, Breakspear M Transl Psychiatry. 2023; 13(1):77.

PMID: 36864034 PMC: 9981770. DOI: 10.1038/s41398-023-02381-x.