Premium
Plasma Levels of Apolipoprotein E and Cognitive Function in Old Age
Author(s) -
MOOIJAART SIMON P.,
VAN VLIET PETER,
VAN HEEMST DIANA,
RENSEN PATRICK C. N.,
BERBÉE JIMMY F. P.,
JOLLES JELLE,
DE CRAEN ANTON J. M.,
WESTENDORP RUDI G. J.
Publication year - 2007
Publication title -
annals of the new york academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.712
H-Index - 248
eISSN - 1749-6632
pISSN - 0077-8923
DOI - 10.1196/annals.1395.013
Subject(s) - apolipoprotein e , medicine , population , dementia , allele , cognitive decline , cognition , psychology , endocrinology , psychiatry , disease , genetics , biology , environmental health , gene
: The relationship between structural variants of the apolipoprotein E gene, APOE ɛ2/ɛ3/ɛ4, and dementia is well established, whereas the relationship of plasma apoE levels with dementia is less clear. Plasma apoE levels are under tight genetic control but vary widely within the various genotypes indicating that the APOE ɛ2/ɛ3/ɛ4 locus explains only a small fraction of this variation. Here we studied the association of plasma apolipoprotein E (apoE) levels with cognitive function in the elderly population at large. Within the Leiden 85‐plus Study, a prospective population‐based study of subjects aged 85 years, we measured plasma apoE level and genotype at base line. During a 5‐year follow‐up period, cognitive function was annually assessed using the Mini Mental State Examination (MMSE) and a standardized neuropsychological test battery. Among ɛ3ɛ3 carriers ( n = 324), high plasma apoE levels associated with impaired global cognitive function (–1.10 points change in MMSE score per one standard deviation increase of plasma apoE level, P = 0.001), as well as lower attention ( P = 0.064), speed and memory function (all P < 0.05). Adjustment for cardiovascular risk factors and exclusion of all subjects who suffered a stroke did not materially change the associations. Similar estimates were obtained in ɛ3ɛ4 carriers ( n = 100), but not in ɛ2ɛ3 carriers ( n = 90). We conclude that in old age, in non‐ɛ2‐allele carriers, high plasma apoE levels are associated with cognitive impairments, independent of genotype, cardiovascular risk factors, and stroke.