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Dissociable Impairments of Verbal Learning Differentiate Childhood Risk Profiles for Schizophrenia

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Specialty Psychology
Date 2022 Mar 4
PMID 35242608
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Abstract

Poor verbal learning and memory function is well-documented among individuals with schizophrenia and those at clinical high-risk for psychosis. This study aimed to identify these impairments among children aged 9-12 years with different schizophrenia risk profiles (family history or antecedents of schizophrenia, each of higher or lower risk load) relative to typically developing peers. These three groups were recruited via community-screening, and differentiated for analysis into: typically developing children (TD = 45); children who had 1 first- or ≥2 second-degree affected relatives (FHx = 16) or one second-degree relative (FHx = 15); and children presenting multiple replicated antecedents of schizophrenia whose clinical symptoms persisted at 2- and/or 4-year follow-up (ASz = 16) or remitted during follow-up (ASz = 16). Verbal learning/memory measures assessed at baseline (age 9-12 years) included: (i) total recall; (ii) trial 1 recall; (iii) learning score; (iv) intrusions; (v) total words lost; and (vi) serial position patterns. Analyses of variance indicated that FHx and ASz youth demonstrated impaired total recall compared to TD and ASz children and lost significantly more words between trials than TD and FHx children. Learning score was impaired among both FHx and FHx relative to TD and ASz children. Thus, among putatively at-risk children, total words recalled and lost distinguished those with higher risk load (by family history or persistent antecedent symptomology), whereas learning score indexed familial vulnerability. Follow-up of the sample is needed to determine the capacity of verbal learning deficits to predict later illness and provide a potential avenue for early remediation to improve clinical or functional outcomes.

Citing Articles

Clinical and functional outcomes at 7-year follow-up of children presenting putative antecedents of schizophrenia at age 9-12 years.

Cullen A, Roberts R, Fisher H, Laurens K Schizophrenia (Heidelb). 2024; 10(1):83.

PMID: 39349507 PMC: 11442655. DOI: 10.1038/s41537-024-00507-8.

References
1.
Addington J, Liu L, Perkins D, Carrion R, Keefe R, Woods S . The Role of Cognition and Social Functioning as Predictors in the Transition to Psychosis for Youth With Attenuated Psychotic Symptoms. Schizophr Bull. 2016; 43(1):57-63. PMC: 5216866. DOI: 10.1093/schbul/sbw152. View

2.
Myles-Worsley M, Ord L, Ngiralmau H, Weaver S, Blailes F, Faraone S . The Palau Early Psychosis Study: neurocognitive functioning in high-risk adolescents. Schizophr Res. 2006; 89(1-3):299-307. DOI: 10.1016/j.schres.2006.08.003. View

3.
Ozan E, Deveci E, Oral M, Karahan U, Oral E, Aydin N . Neurocognitive functioning in a group of offspring genetically at high-risk for schizophrenia in Eastern Turkey. Brain Res Bull. 2010; 82(3-4):218-23. DOI: 10.1016/j.brainresbull.2010.04.013. View

4.
Blachstein H, Vakil E . Verbal learning across the lifespan: an analysis of the components of the learning curve. Neuropsychol Dev Cogn B Aging Neuropsychol Cogn. 2015; 23(2):133-53. DOI: 10.1080/13825585.2015.1063579. View

5.
Fisher H, Caspi A, Poulton R, Meier M, Houts R, Harrington H . Specificity of childhood psychotic symptoms for predicting schizophrenia by 38 years of age: a birth cohort study. Psychol Med. 2013; 43(10):2077-86. PMC: 3758773. DOI: 10.1017/S0033291712003091. View