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APOE ε2 allele is associated with larger regional cortical thicknesses and volumes.

TitleAPOE ε2 allele is associated with larger regional cortical thicknesses and volumes.
Publication TypeJournal Article
Year of Publication2010
AuthorsLiu, Y., Paajanen T., Westman E., Zhang Y., Wahlund L-O., Simmons A., Tunnard C., Sobow T., Proitsi P., Powell J., Mecocci P., Tsolaki M., Vellas B., Muehlboeck S., Evans A., Spenger C., Lovestone S., & Soininen H.
Corporate AuthorsAddNeuroMed Consortium
JournalDement Geriatr Cogn Disord
Volume30
Issue3
Pagination229-37
Date Published2010
ISSN1421-9824
KeywordsAge of Onset, Aged, Alleles, Alzheimer Disease, Apolipoprotein E2, Brain, Cerebral Cortex, Cognition Disorders, Data Interpretation, Statistical, Female, Gene Frequency, Genotype, Heterozygote, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Neuropsychological Tests
Abstract

BACKGROUND: The protective effect of the apolipoprotein E (APOE) ε2 allele against Alzheimer's disease (AD) is controversial.OBJECTIVE: Our purpose was to clarify if the ε2 allele affects regional cortical thicknesses and volumes.METHODS: Regional cortical thicknesses and volumes were measured with an automated pipeline in 109 subjects with mild cognitive impairment, 114 AD patients and 105 age-matched healthy controls.RESULTS: In the mild cognitive impairment group, the ε2 carriers had thicker regional cortices at the transverse temporal cortex and parahippocampal gyrus than the subjects with ε3/ε3, and a larger cerebral gray matter and smaller lateral ventricles than the ε3/ε3 and ε4 carriers. In the AD group, the ε2 carriers had significantly thicker entorhinal and transverse temporal cortices, a larger whole cerebral gray matter, and smaller lateral ventricles than the subjects with the ε3/ε3 genotype, and a significantly thicker entorhinal cortex and larger cerebral gray matter than ε4 carriers. No APOE2 effect was found in the control group.CONCLUSION: The APOE ε2 allele is associated with larger regional cortical thicknesses and volumes in mild cognitive impairment and AD.

DOI10.1159/000320136
Alternate JournalDement Geriatr Cogn Disord
PubMed ID20847553

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