| Literature DB >> 24883238 |
Mary Ann A DeMichele-Sweet1, Robert A Sweet2.
Abstract
Psychosis occurs in approximately half of patients with Alzheimer disease (AD with psychosis, AD+P). AD+P patients have more rapid cognitive decline, greater behavioral symptoms, and higher mortality than do AD patients without psychosis. Studies in three independent cohorts have shown that psychosis in AD aggregates in families, with estimated heritability of 29.5 - 60.8%. These findings have motivated studies to investigate and uncover the genes responsible for the development of psychosis, with the ultimate goal of identifying potential biologic mechanisms that may serve as leads to specific therapies. Linkage analyses have implicated loci on chromosomes 2, 6, 7, 8, 15, and 21 with AD+P. Association studies of APOE do not support it as a risk gene for psychosis in AD. No other candidate genes, such as neurodegenerative and monoamine genes, show conclusive evidence of association with AD+P. However, a recent genome-side association study has produced some promising leads, including among them genes that have been associated with schizophrenia. This review summarizes the current knowledge of the genetic basis of AD+P.Entities:
Keywords: Alzheimer disease; Association Study; Genome-wide association; Heritability; Linkage Analysis; Psychosis
Year: 2014 PMID: 24883238 PMCID: PMC4034371 DOI: 10.1007/s40142-014-0030-1
Source DB: PubMed Journal: Curr Genet Med Rep ISSN: 2167-4876