Mutations modifying sporadic Alzheimer's disease age of onset
Autor: | Yeping Cai, Claudio A. Mastronardi, Andrés Villegas, Shaun G. Lehmann, Jorge I. Vélez, Hardip R. Patel, Diego Sepulveda-Falla, Francisco Lopera, Mauricio Arcos-Burgos, Dora Rivera, Simon Easteal, Angad S. Johar, Carlos Tobon |
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Rok vydání: | 2015 |
Předmět: |
0301 basic medicine
Male Genotype Disease Biology Neuron apoptosis 03 medical and health sciences Cellular and Molecular Neuroscience Alzheimer Disease PSEN1 Humans Exome Genetic Predisposition to Disease Age of Onset Gene Genetics (clinical) Aged Genetics Neurogenesis Oligodendrocyte differentiation Middle Aged Psychiatry and Mental health 030104 developmental biology Mutation Female Age of onset Genetic isolate Genome-Wide Association Study |
Zdroj: | American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 171(8) |
ISSN: | 1552-485X |
Popis: | The identification of mutations modifying the age of onset (AOO) in Alzheimer's disease (AD) is crucial for understanding the natural history of AD and, therefore, for early interventions. Patients with sporadic AD (sAD) from a genetic isolate in the extremes of the AOO distribution were whole-exome genotyped. Single- and multi-locus linear mixed-effects models were used to identify functional variants modifying AOO. A posteriori enrichment and bioinformatic analyses were applied to evaluate the non-random clustering of the associate variants to physiopathological pathways involved in AD. We identified more than 20 pathogenic, genome-wide statistically significant mutations of major modifier effect on the AOO. These variants are harbored in genes implicated in neuron apoptosis, neurogenesis, inflammatory processes linked to AD, oligodendrocyte differentiation, and memory processes. This set of new genes harboring these mutations could be of importance for prediction, follow-up and eventually as therapeutical targets of AD. © 2016 Wiley Periodicals, Inc. |
Databáze: | OpenAIRE |
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