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Dissociable impairments of verbal learning differentiate childhood risk profiles for schizophrenia
被引:3
|作者:
Carpendale, Emma J.
[1
]
Cullen, Alexis E.
[2
]
Dickson, Hannah
[3
]
Laurens, Kristin R.
[1
,2
,4
]
机构:
[1] Queensland Univ Technol QUT, Sch Psychol & Counselling, Brisbane, Qld, Australia
[2] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychosis Studies, London, England
[3] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Forens & Neurodev Sci, London, England
[4] Univ New South Wales, Sch Psychiat, Sydney, NSW, Australia
来源:
SCHIZOPHRENIA RESEARCH-COGNITION
|
2022年
/
28卷
基金:
澳大利亚研究理事会;
关键词:
Psychosis;
Genetic liability;
Memory;
Cognition;
High-risk;
PSYCHOTIC-LIKE EXPERIENCES;
COGNITIVE REMEDIATION;
CHILDREN;
NEUROCOGNITION;
1ST-EPISODE;
PRODROME;
MEMORY;
YOUTH;
METAANALYSIS;
DISORDER;
D O I:
10.1016/j.scog.2022.100239
中图分类号:
R749 [精神病学];
学科分类号:
100205 ;
摘要:
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([H]) or lower([L]) 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(H) = 16) or one second-degree relative (FHx(L) = 15); and children presenting multiple replicated antecedents of schizophrenia whose clinical symptoms persisted at 2- and/or 4-year follow-up (ASz(H) = 16) or remitted during follow-up (ASz(L) = 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(H) and ASz(H) youth demonstrated impaired total recall compared to TD and ASz(L) children and lost significantly more words between trials than TD and FHx(L) children. Learning score was impaired among both FHx(H) and FHx(L) relative to TD and ASz(L) 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.
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