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
相关论文
共 39 条
[1]   Risk for Alzheimer's disease correlates with transcriptional activity of the APOE gene [J].
Artiga, MJ ;
Bullido, MJ ;
Frank, A ;
Sastre, I ;
Recuero, M ;
Garcia, MA ;
Lendon, CL ;
Han, SW ;
Morris, JC ;
Vázquez, J ;
Goate, A ;
Valdivieso, F .
HUMAN MOLECULAR GENETICS, 1998, 7 (12) :1887-1892
[2]  
Beekman M, 2002, TWIN RES, V5, P87, DOI 10.1375/twin.5.2.87
[3]   Apolipoprotein E and β-amyloid levels in the hippocampus and frontal cortex of Alzheimer's disease subjects are disease-related and apolipoprotein E genotype dependent [J].
Beffert, U ;
Cohn, JS ;
Petit-Turcotte, C ;
Tremblay, M ;
Aumont, N ;
Ramassamy, C ;
Davignon, J ;
Poirier, J .
BRAIN RESEARCH, 1999, 843 (1-2) :87-94
[4]  
BLUM CB, 1982, J LIPID RES, V23, P1308
[5]   Structural and functional variations in human apolipoprotein E3 and E4 [J].
Chou, CY ;
Jen, WP ;
Hsieh, YH ;
Shiao, MS ;
Chang, GG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (19) :13333-13344
[6]   GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES [J].
CORDER, EH ;
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, DE ;
GASKELL, PC ;
SMALL, GW ;
ROSES, AD ;
HAINES, JL ;
PERICAKVANCE, MA .
SCIENCE, 1993, 261 (5123) :921-923
[7]   Apolipoprotein E polymorphism and cardiovascular disease: A HuGE review [J].
Eichner, JE ;
Dunn, ST ;
Perveen, G ;
Thompson, DM ;
Stewart, KE ;
Stroehla, BC .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2002, 155 (06) :487-495
[8]  
Folin M, 2004, INT J MOL MED, V14, P609
[9]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499
[10]   Role of genes and environments for explaining Alzheimer disease [J].
Gatz, M ;
Reynolds, CA ;
Fratiglioni, L ;
Johansson, B ;
Mortimer, JA ;
Berg, S ;
Fiske, A ;
Pedersen, NL .
ARCHIVES OF GENERAL PSYCHIATRY, 2006, 63 (02) :168-174