Hostname: page-component-586b7cd67f-gb8f7 Total loading time: 0 Render date: 2024-11-29T12:28:42.648Z Has data issue: false hasContentIssue false

Kibra Allelic Variation is Associated with Memory Processes in Early Onset Schizophrenia

Published online by Cambridge University Press:  16 April 2020

N.S. Vyas
Affiliation:
Section of Neurobiology of Psychosis, Division of Psychological Medicine, London, UK
L. Burke
Affiliation:
Section of Neurobiology of Psychosis, Division of Psychological Medicine, London, UK
A. Vourdas
Affiliation:
Section of Neurobiology of Psychosis, Division of Psychological Medicine, London, UK
E. Vassos
Affiliation:
MRC Social Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, London, UK
S. Frangou
Affiliation:
Section of Neurobiology of Psychosis, Division of Psychological Medicine, London, UK
D.A. Collier
Affiliation:
MRC Social Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, London, UK

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Background:

A single nucleotide polymorphism, rs17070145, in the KIBRA protein, is thought to influence memory function in humans (Papassotiropoulos et al, 2006). We sought to investigate its effect on memory performance in people with Early Onset Schizophrenia (EOS; onset before age of 18) and their first-degree relatives.

Methods:

53 EOS probands and 117 non-psychotic first-degree relatives were examined on IQ (Wechsler Adult Intelligence Scale-Revised), learning and memory (California Verbal Learning Test; CVLT). the Structured Clinical Interview for DSM-IV yielded four diagnostic groups: EOS probands; relatives with Mood Disorders; other Axis I diagnoses; and no diagnosis (healthy relatives). Analysis of co-variance was performed, with diagnosis and genotype as fixed factors and age as covariate.

Results:

Carriers of the rs17070145 T allele achieved higher performance IQ, and recalled more words in short-delayed and long-delayed recall in the CVLT compared to C allele carriers [p< 0.003 and p< 0.009, respectively]. However TT homozygotes made more perseverative errors than C allele carriers [p=0.04]. after applying the Bonferroni for multiple comparisons, a genotype by diagnosis interaction revealed that relatives who were TT homozygotes and had mood disorders performed better on long-delayed recall [p< 0.04] but made more intrusion errors in the CVLT than the CC/CT genotype group.

Conclusions:

KIBRA may be involved in:

  1. 1. processes that enhance overall competence in non-verbal tasks;

  2. 2. phenotypic expression of cognition in mentally unwell relatives of schizophrenia patients.

Type
P03-217
Copyright
Copyright © European Psychiatric Association 2009

References

Reference:

Papassotiropoulos, A., Stephan, D.A. Huentelman, , et al. (2006). Common Kibra Alleles are Associated with Human Memory Performance. Science 314, 475478CrossRefGoogle ScholarPubMed
Submit a response

Comments

No Comments have been published for this article.