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@ARTICLE{Vglein:140511,
author = {Vöglein, Jonathan and Noachtar, Soheyl and McDade, Eric
and Quaid, Kimberly A and Salloway, Stephen and Ghetti,
Bernardino and Noble, James and Berman, Sarah and Chhatwal,
Jasmeer and Mori, Hiroshi and Fox, Nick and Allegri, Ricardo
and Masters, Colin L and Buckles, Virginia and Ringman, John
M and Rossor, Martin and Schofield, Peter R and Sperling,
Reisa and Jucker, Mathias and Laske, Christoph and Paumier,
Katrina and Morris, John C and Bateman, Randall J and Levin,
Johannes and Danek, Adrian and Network, Dominantly Inherited
Alzheimer},
title = {{S}eizures as an early symptom of autosomal dominant
{A}lzheimer's disease.},
journal = {Neurobiology of aging},
volume = {76},
issn = {0197-4580},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {DZNE-2020-06833},
pages = {18-23},
year = {2019},
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.},
keywords = {Adult / Alzheimer Disease: complications / Alzheimer
Disease: genetics / Female / Genes, Dominant: genetics /
Genetic Association Studies / Heterozygote / Humans / Male /
Mutation: genetics / Observational Studies as Topic /
Predictive Value of Tests / Risk / Seizures: etiology /
Seizures: genetics},
cin = {AG Höglinger 1 / AG Jucker / AG Levin / U Clinical
Researchers - München},
ddc = {610},
cid = {I:(DE-2719)1110002 / I:(DE-2719)1210001 /
I:(DE-2719)1111016 / I:(DE-2719)7000003},
pnm = {344 - Clinical and Health Care Research (POF3-344) / 342 -
Disease Mechanisms and Model Systems (POF3-342)},
pid = {G:(DE-HGF)POF3-344 / G:(DE-HGF)POF3-342},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30616208},
pmc = {pmc:PMC6572755},
doi = {10.1016/j.neurobiolaging.2018.11.022},
url = {https://pub.dzne.de/record/140511},
}