| Literature DB >> 30616208 |
Jonathan Vöglein1, Soheyl Noachtar2, Eric McDade3, Kimberly A Quaid4, Stephen Salloway5, Bernardino Ghetti6, James Noble7, Sarah Berman8, Jasmeer Chhatwal9, Hiroshi Mori10, Nick Fox11, Ricardo Allegri12, Colin L Masters13, Virginia Buckles3, John M Ringman14, Martin Rossor11, Peter R Schofield15, Reisa Sperling9, Mathias Jucker16, Christoph Laske17, Katrina Paumier3, John C Morris3, Randall J Bateman3, Johannes Levin18, Adrian Danek19.
Abstract
Our objective was to assess the reported history of seizures in cognitively asymptomatic mutation carriers for autosomal dominant Alzheimer's disease (ADAD) and the predictive value of seizures for mutation carrier status in cognitively asymptomatic first-degree relatives of ADAD patients. Seizure occurrence in the Dominantly Inherited Alzheimer Network observational study was correlated with mutation carrier status in cognitively asymptomatic subjects. Of 276 cognitively asymptomatic individuals, 11 (4%) had experienced seizures, and nine of these carried an ADAD mutation. Thus, in the Dominantly Inherited Alzheimer Network population, seizure frequency in mutation carriers was significantly higher than in noncarriers (p = 0.04), and the positive predictive value of seizures for the presence of a pathogenic mutation was 81.8%. Among cognitively asymptomatic ADAD family members, the occurrence of seizures increases the a priori risk of 50% mutation-positive status to about 80%. This finding suggests that ADAD mutations increase the risk of seizures.Entities:
Keywords: Alzheimer's disease; Autosomal dominant; Dementia; Genetics; Positive predictive value; Seizures
Mesh:
Year: 2018 PMID: 30616208 PMCID: PMC6572755 DOI: 10.1016/j.neurobiolaging.2018.11.022
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 5.133