Alzheimer's disease: Interaction of apolipoprotein E genotype, family history of dementia, gender, education, ethnicity, and age of onset

被引:118
作者
Duara, R
Barker, WW
LopezAlberola, R
Loewenstein, DA
Grau, LB
Gilchrist, D
Sevush, S
StGeorgeHyslop, PH
机构
[1] UNIV MIAMI,SCH MED,DEPT MED & NEUROL,MIAMI,FL
[2] UNIV MIAMI,SCH MED,DEPT PSYCHIAT,MIAMI,FL
[3] UNIV TORONTO,DEPT MED,DIV NEUROL,CTR RES NEURODEGENERAT DIS,TORONTO,ON,CANADA
[4] UNIV TORONTO,DEPT PHYSIOL,DIV NEUROL,CTR RES NEURODEGENERAT DIS,TORONTO,ON,CANADA
关键词
D O I
10.1212/WNL.46.6.1575
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We evaluated 197 patients with predominantly late-onset Alzheimer's disease (AD) who belonged to several ethnic groups and analyzed the relationship of age of onset of AD to the presence or absence of several risk factors in this entire group of patients. The apolipoprotein E (apoE) epsilon 4 allele frequency, which was 29% in all patients (compared with the reported population mean of 13.7%, p < 0.001, did not vary significantly between ethnic groups but declined significantly with increasing age. The apoE epsilon 2 allele frequency was 3%, compared with the reported population mean of 7.4% (p = 0.001). The frequency of a positive family history of dementia in first-degree relatives (FH+) (overall 45%) did not vary significantly between ethnic groups. ApoE epsilon 4-positive (epsilon 4+) patients tended to have a higher FH+ rate (58%) than apoE epsilon 4-negative (epsilon 4-) patients (40%) (p = 0.02). When the potential risk factors of gender, education, FH+ status, and epsilon 4+ status were examined together in a multiple linear-regression analysis, FH+ and epsilon 4+ status (but not gender or education) were significant (they were both associated with an earlier age of onset of AD). In a post-hoc analysis, we found a reduced age of onset in women, but not men, who were both FH+ and epsilon 4+. Additionally, those probands who were epsilon 4+ were more likely to inherit the disease from their mothers than their fathers. The mechanism by which epsilon 4+ and FH+ status operate as risk factors may be by their effect on the age of onset of AD.
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页码:1575 / 1579
页数:5
相关论文
共 30 条
[21]   APOLIPOPROTEIN-E POLYMORPHISM AND ALZHEIMERS-DISEASE [J].
POIRIER, J ;
DAVIGNON, J ;
BOUTHILLIER, D ;
KOGAN, S ;
BERTRAND, P ;
GAUTHIER, S .
LANCET, 1993, 342 (8873) :697-699
[22]   REDUCED APOLIPOPROTEIN EPSILON-4 ALLELE FREQUENCY IN THE OLDEST-OLD ALZHEIMERS PATIENTS AND COGNITIVELY NORMAL INDIVIDUALS [J].
REBECK, GW ;
PERLS, TT ;
WEST, HL ;
SODHI, P ;
LIPSITZ, LA ;
HYMAN, BT .
NEUROLOGY, 1994, 44 (08) :1513-1516
[23]   FREQUENCY AND DISTRIBUTION OF ALZHEIMERS-DISEASE IN EUROPE - A COLLABORATIVE STUDY OF 1980-1990 PREVALENCE FINDINGS [J].
ROCCA, WA ;
HOFMAN, A ;
BRAYNE, C ;
BRETELER, MMB ;
CLARKE, M ;
COPELAND, JRM ;
DARTIGUES, JF ;
ENGEDAL, K ;
HAGNELL, O ;
HEEREN, TJ ;
JONKER, C ;
LINDESAY, J ;
LOBO, A ;
MANN, AH ;
MOLSA, PK ;
MORGAN, K ;
OCONNOR, DW ;
DROUX, AD ;
SULKAVA, R ;
KAY, DWK ;
AMADUCCI, L .
ANNALS OF NEUROLOGY, 1991, 30 (03) :381-390
[24]   ASSOCIATION OF APOLIPOPROTEIN-E ALLELE EPSILON-4 WITH LATE-ONSET FAMILIAL AND SPORADIC ALZHEIMERS-DISEASE [J].
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, D ;
GEORGEHYSLOP, PHS ;
PERICAKVANCE, MA ;
JOO, SH ;
ROSI, BL ;
GUSELLA, JF ;
CRAPPERMACLACHLAN, DR ;
ALBERTS, MJ ;
HULETTE, C ;
CRAIN, B ;
GOLDGABER, D ;
ROSES, AD .
NEUROLOGY, 1993, 43 (08) :1467-1472
[25]   APOLIPOPROTEIN-E POLYMORPHISM IN THE NETHERLANDS AND ITS EFFECT ON PLASMA-LIPID AND APOLIPOPROTEIN LEVELS [J].
SMIT, M ;
DEKNIJFF, P ;
ROSSENEU, M ;
BURY, J ;
KLASEN, E ;
FRANTS, R ;
HAVEKES, L .
HUMAN GENETICS, 1988, 80 (03) :287-292
[26]   LACK OF ASSOCIATION OF APOLIPOPROTEIN-E ALLELE EPSILON-4 WITH LATE-ONSET ALZHEIMERS-DISEASE AMONG FINNISH CENTENARIANS [J].
SOBEL, E ;
LOUHIJA, J ;
SULKAVA, R ;
DAVANIPOUR, Z ;
KONTULA, K ;
MIETTINEN, H ;
TIKKANEN, M ;
KAINULAINEN, K ;
TILVIS, R .
NEUROLOGY, 1995, 45 (05) :903-907
[27]   APOLIPOPROTEIN-E - HIGH-AVIDITY BINDING TO BETA-AMYLOID AND INCREASED FREQUENCY OF TYPE-4 ALLELE IN LATE-ONSET FAMILIAL ALZHEIMER-DISEASE [J].
STRITTMATTER, WJ ;
SAUNDERS, AM ;
SCHMECHEL, D ;
PERICAKVANCE, M ;
ENGHILD, J ;
SALVESEN, GS ;
ROSES, AD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :1977-1981
[28]   ARE THE ASSOCIATIONS BETWEEN ALZHEIMERS-DISEASE AND POLYMORPHISMS IN THE APOLIPOPROTEIN-E AND THE APOLIPOPROTEIN-CII GENES DUE TO LINKAGE DISEQUILIBRIUM [J].
TSUDA, T ;
LOPEZ, R ;
ROGAEVA, EA ;
FREEDMAN, M ;
ROGAEV, E ;
DRACHMAN, D ;
POLLEN, D ;
HAINES, J ;
LIANG, Y ;
MCLACHLAN, DRC ;
DUARA, R ;
STGEORGEHYSLOP, P .
ANNALS OF NEUROLOGY, 1994, 36 (01) :97-100
[29]   THE CLINICAL-DIAGNOSIS OF ALZHEIMERS-DISEASE [J].
WADE, JPH ;
MIRSEN, TR ;
HACHINSKI, VC ;
FISMAN, M ;
LAU, C ;
MERSKEY, H .
ARCHIVES OF NEUROLOGY, 1987, 44 (01) :24-29
[30]  
1993, FL STAT ABSTR, P26