Cortical Gyrification, Psychotic-Like Experiences, and Cognitive Performance in Nonclinical Subjects. (21st July 2020)

• Record Type: Journal Article
• Authors: Evermann, Ulrika; Gaser, Christian; Besteher, Bianca; Langbein, Kerstin; Nenadić, Igor
• Is Part Of: Schizophrenia bulletin. Volume 46:Number 6(2020)
• Page Start: 1524
• Page End: 1534
• Publication Date: 2020-07-21
• Subjects: cognitive function -- endophenotype -- neurodevelopment -- subclinical -- magnetic resonance imaging (MRI); Schizophrenia -- Periodicals; Schizophrenia -- Research -- Periodicals; 616.898005
• DOI: 10.1093/schbul/sbaa068
• Languages: English
• ISSNs: 0586-7614

Abstract

Abstract: Background: Psychotic-like experiences (PLE) are present in nonclinical populations, yet their association with brain structural variation, especially markers of early neurodevelopment, is poorly understood. We tested the hypothesis that cortical surface gyrification, a putative marker of early brain development, is associated with PLE in healthy subjects. Methods: We analyzed gyrification from 3 Tesla MRI scans (using CAT12 software) and PLE (positive, negative, and depressive symptom dimensions derived from the Community Assessment of Psychic Experiences, CAPE) in 103 healthy participants (49 females, mean age 29.13 ± 9.37 years). A subsample of 63 individuals completed tasks from the Wechsler Adult Intelligence Scale and Controlled Oral Word Association Test. Estimated IQ and a composite neuropsychological score were used to explore mediation pathways via cognition. Results: Positive PLE distress was negatively associated with gyrification of the left precuneus. PLE depression dimension showed a negative association with gyrification in the right supramarginal and temporal region. There was no significant mediating effect of cognition on these associations. Conclusion: Our results support a neurobiological psychosis spectrum, for the first time linking an early developmental imaging marker (rather than volume) to dimensional subclinical psychotic symptoms. While schizophrenia risk, neurodevelopment, and cognitive function might share genetic risk factors, additional mediation analyses did not confirm a mediating effect of cognition on the gyrification-psychopathology correlation.