TY - JOUR
T1 - ApoE E4 is a Susceptibility Factor in Amnestic but Not Aphasic Dementias
AU - Rogalski, Emily Joy
AU - Rademaker, Alfred
AU - Harrison, Theresa M.
AU - Helenowski, Irene
AU - Johnson, Nancy
AU - Bigio, Eileen
AU - Mishra, Manjari
AU - Weintraub, Sandra
AU - Mesulam, Marek Marsel
PY - 2011/4
Y1 - 2011/4
N2 - The goal of this study was to determine if the apolipoprotein ε gene, which is a well-established susceptibility factor for Alzheimer disease (AD) pathology in typical amnestic dementias, may also represent a risk factor in the language-based dementia, primary progressive aphasia (PPA). Apolipoprotein E genotyping was obtained from 149 patients with a clinical diagnosis of PPA, 330 cognitively healthy individuals (NC), and 179 patients with a clinical diagnosis of probable Alzheimer's disease (PrAD). Allele frequencies were compared among the groups. Analyses were also completed by sex and in 2 subsets of PPA patients: 1 in which the patients were classified by subtype (logopenic, agrammatic, and semantic) and another in which pathologic data were available. The allele frequencies for the PPA group (ε2:5%, ε3:79.5%, and ε4:15.4%) showed a distribution similar to the NC group, but significantly different from the PrAD group. The presence of an ε4 allele did not influence the age of symptom onset or aid in the prediction of AD pathology in PPA. These data show that ε4 polymorphism, which is a well-known risk factor for AD pathology in typical amnestic dementias, has no similar relationship to the clinical syndrome of PPA or its association with AD pathology.
AB - The goal of this study was to determine if the apolipoprotein ε gene, which is a well-established susceptibility factor for Alzheimer disease (AD) pathology in typical amnestic dementias, may also represent a risk factor in the language-based dementia, primary progressive aphasia (PPA). Apolipoprotein E genotyping was obtained from 149 patients with a clinical diagnosis of PPA, 330 cognitively healthy individuals (NC), and 179 patients with a clinical diagnosis of probable Alzheimer's disease (PrAD). Allele frequencies were compared among the groups. Analyses were also completed by sex and in 2 subsets of PPA patients: 1 in which the patients were classified by subtype (logopenic, agrammatic, and semantic) and another in which pathologic data were available. The allele frequencies for the PPA group (ε2:5%, ε3:79.5%, and ε4:15.4%) showed a distribution similar to the NC group, but significantly different from the PrAD group. The presence of an ε4 allele did not influence the age of symptom onset or aid in the prediction of AD pathology in PPA. These data show that ε4 polymorphism, which is a well-known risk factor for AD pathology in typical amnestic dementias, has no similar relationship to the clinical syndrome of PPA or its association with AD pathology.
KW - Alzheimer disease
KW - Primary progressive aphasia
KW - frontotemporal dementia
KW - genetics
KW - genotype
KW - pathology
KW - risk factor
UR - http://www.scopus.com/inward/record.url?scp=79958274677&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79958274677&partnerID=8YFLogxK
U2 - 10.1097/WAD.0b013e318201f249
DO - 10.1097/WAD.0b013e318201f249
M3 - Article
C2 - 21346518
AN - SCOPUS:79958274677
SN - 0893-0341
VL - 25
SP - 159
EP - 163
JO - Alzheimer Disease and Associated Disorders
JF - Alzheimer Disease and Associated Disorders
IS - 2
ER -