Parental history of Alzheimer disease associated with lower plasma apolipoprotein E levels

被引:21
|
作者
van Vliet, P. [1 ]
Westendorp, R. G. J. [1 ]
Eikelenboom, P. [4 ,5 ]
Comijs, H. C. [4 ]
Froelich, M. [2 ]
Bakker, E. [3 ]
van der Flier, W. [6 ]
van Exel, E. [4 ]
机构
[1] Leiden Univ, Med Ctr, Dept Gerontol & Geriatr, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Clin Chem, NL-2300 RC Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Clin Genet, Ctr Human & Clin Genet, NL-2300 RC Leiden, Netherlands
[4] VU Med Ctr SGB, Dept Psychiat, Amsterdam, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Dept Neurol, NL-1105 AZ Amsterdam, Netherlands
[6] Vrije Univ Amsterdam Med Ctr, Dept Neurol, Amsterdam, Netherlands
关键词
E APOE LEVELS; CEREBROSPINAL-FLUID; COGNITIVE FUNCTION; E POLYMORPHISM; E RESPONSE; OLD-AGE; RISK; GENE; CHOLESTEROL; DEMENTIA;
D O I
10.1212/WNL.0b013e3181b59c2e
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Variation in APOE genotype is a determinant of Alzheimer disease (AD), but the risk associated with variation in plasma apoE levels has yet to be determined. Here, we studied offspring with and without a parental history of AD to identify the effect of plasma apoE levels at middle age on the risk of late-onset AD. Methods: Some 203 offspring from 92 families with a parental history of AD were compared with 197 offspring from 97 families without a parental history of AD. APOE genotypes and plasma apoE levels were assessed in all offspring. Difference in plasma apoE level between subjects with and without a parental history of AD was calculated using robust linear regression, both stratified and adjusted for APOE genotype. Results: Offspring with a parental history of AD were more likely to be an APOE epsilon 4 allele carrier (46% vs 21%, p < 0.001) than offspring without such a parental history. Mean plasma apoE levels strongly decreased from epsilon 2 to epsilon 3 epsilon 3 to epsilon 4 carriers (p < 0.001). Offspring with a parental history of AD had lower plasma apoE levels than subjects without such a history, both in analyses adjusted for APOE genotype (difference: -0.21 mg/dL, p = 0.02) and when using standardized Z scores, when stratified for APOE genotype (difference: -0.22, p = 0.009). Conclusions: Our findings suggest that lower plasma apoE levels in middle age could be a risk factor for Alzheimer disease in old age, independent of APOE genotype. Neurology (R) 2009; 73: 681-687
引用
收藏
页码:681 / 687
页数:7
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