EIF2AK3 variants in Dutch patients with Alzheimer's disease

Next-generation sequencing has contributed to our understanding of the genetics of Alzheimer's disease (AD) and has explained a substantial part of the missing heritability of familial AD. We sequenced 19 exomes from 8 Dutch families with a high AD burden and identified EIF2AK3, encoding for protein kinase RNA-like endoplasmic reticulum kinase (PERK), as a candidate gene. Gene-based burden analysis in a Dutch AD exome cohort containing 547 cases and 1070 controls showed a significant association of EIF2AK3 with AD (OR 1.84 [95% CI 1.07–3.17], p-value 0.03), mainly driven by the variant p.R240H... Mehr ...

Verfasser: Wong, Tsz Hang
van der Lee, Sven J.
van Rooij, Jeroen G.J.
Meeter, Lieke H.H.
Frick, Petra
Melhem, Shamiram
Seelaar, Harro
Ikram, M. Arfan
Rozemuller, Annemieke J.
Holstege, Henne
Hulsman, Marc
Uitterlinden, Andre
Neumann, Manuela
Hoozemans, Jeroen J.M.
van Duijn, Cornelia M.
Rademakers, Rosa
van Swieten, John C.
Dokumenttyp: Artikel
Erscheinungsdatum: 2019
Schlagwörter: Alzheimer's disease / EIF2AK3 / Exome sequencing / PERK / eIF-2 Kinase/genetics / Genetic Association Studies / Alzheimer Disease/genetics / Humans / Middle Aged / Male / Risk / Genetic Variation/genetics / Whole Exome Sequencing / Netherlands / Hippocampus/metabolism / Female / Aged / Clinical Neurology / Geriatrics and Gerontology / Ageing / General Neuroscience / Developmental Biology / Research Support / Non-U.S. Gov't / Journal Article
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29202596
Datenquelle: BASE; Originalkatalog
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Link(s) : https://dspace.library.uu.nl/handle/1874/391398