Examining the association between genetic liability for schizophrenia and psychotic symptoms in Alzheimer’s disease

Author:

Creese ByronORCID, ,Vassos EvangelosORCID,Bergh Sverre,Athanasiu Lavinia,Johar Iskandar,Rongve Arvid,Medbøen Ingrid Tøndel,Vasconcelos Da Silva Miguel,Aakhus Eivind,Andersen Fred,Bettella FrancescoORCID,Braekhus Anne,Djurovic SrdjanORCID,Paroni Giulia,Proitsi PetroulaORCID,Saltvedt Ingvild,Seripa Davide,Stordal Eystein,Fladby Tormod,Aarsland Dag,Andreassen Ole A.,Ballard Clive,Selbaek GeirORCID

Abstract

Abstract Psychosis (delusions or hallucinations) in Alzheimer’s disease (AD + P) occurs in up to 50% of individuals and is associated with significantly worse clinical outcomes. Atypical antipsychotics, first developed for schizophrenia, are commonly used in AD + P, suggesting shared mechanisms. Despite this implication, little empirical research has been conducted to examine whether there are mechanistic similarities between AD + P and schizophrenia. In this study, we tested whether polygenic risk score (PRS) for schizophrenia was associated with AD + P. Schizophrenia PRS was calculated using Psychiatric Genomics Consortium data at ten GWAS p value thresholds (PT) in 3111 AD cases from 11 cohort studies characterized for psychosis using validated, standardized tools. Association between PRS and AD + P status was tested by logistic regression in each cohort individually and the results meta-analyzed. The schizophrenia PRS was associated with AD + P at an optimum PT of 0.01. The strongest association was for delusions where a one standard deviation increase in PRS was associated with a 1.18-fold increased risk (95% CI: 1.06–1.3; p = 0.001). These new findings point towards psychosis in AD—and particularly delusions—sharing some genetic liability with schizophrenia and support a transdiagnostic view of psychotic symptoms across the lifespan.

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Cellular and Molecular Neuroscience,Psychiatry and Mental health

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