Effects of apolipoprotein E-epsilon4 and -epsilon2 in amnestic mild cognitive impairment and dementia in Shanghai: SCOBHI-P.

TitleEffects of apolipoprotein E-epsilon4 and -epsilon2 in amnestic mild cognitive impairment and dementia in Shanghai: SCOBHI-P.
Publication TypeJournal Article
Year of Publication2010
AuthorsBorenstein AR, Mortimer JA, Schellenberg GD, DeCarli C, Copenhaver C, Galasko D, Salmon DP, Petersen R
JournalAm J Alzheimers Dis Other Demen
Volume25
Issue3
Pagination233-8
Date Published2010 May
ISSN1938-2731
KeywordsAged, Amnesia, Apolipoprotein E2, Apolipoprotein E4, Catchment Area, Health, China, Cognition Disorders, Dementia, Female, Genotype, Humans, Male, Neuropsychological Tests, Severity of Illness Index
Abstract

OBJECTIVE: To determine apolipoprotein E (APOE)-epsilon4 and -epsilon2 frequencies and risk of mild cognitive impairment (MCI) and dementia in Shanghai, China.

METHODS: A total of 34 MCI and 34 dementia cases were recruited from an urban Memory Disorders Clinic and 32 controls were recruited from a residential community served by the clinic. Apolipoprotein E was genotyped using standard methods.

RESULTS: Among controls, frequencies were epsilon2, 0.11; epsilon3, 0.84; and epsilon4, 0.05; among MCI, 0.05, 0.77, and 0.18; and for dementia, 0.02, 0.84, and 0.15, respectively. In education-adjusted models, the odds ratio (OR) = 5.6 for dementia (95% CI = 1.09-29.3) and 4.7 for MCI (95% CI = 0.90-25.2) associated with any epsilon4 allele. The epsilon2 allele was inversely associated with dementia (OR = 0.12, 95% CI = 0.013-0.997) and MCI (OR = 0.38, 95% CI = 0.08-1.61).

CONCLUSIONS: APOE-epsilon4 increases and -epsilon2 decreases the risk of dementia vs normal cognition. Similar trends were observed for amnestic mild cognitive impairment (aMCI).

DOI10.1177/1533317509357736
Alternate JournalAm J Alzheimers Dis Other Demen
PubMed ID20142627
PubMed Central IDPMC2872993
Grant ListR21 AG028182-02 / AG / NIA NIH HHS / United States
P30 AG010129-19 / AG / NIA NIH HHS / United States
R21 AG028182 / AG / NIA NIH HHS / United States
P30 AG010129-18 / AG / NIA NIH HHS / United States
P30 AG010129 / AG / NIA NIH HHS / United States