Apolipoprotein E polymorphism in elderly Chilean people with Alzheimer's disease

被引:19
作者
Quiroga, P
Calvo, C
Albala, C
Urquidi, J
Santos, JL
Pérez, H
Klaassen, G
机构
[1] Univ Concepcion, Sch Med, Concepcion, Chile
[2] Univ Concepcion, Sch Pharm, Concepcion, Chile
[3] Univ Chile, Inst Nutr & Food Technol, Santiago, Chile
关键词
dementia; Alzheimer's disease; ApoE alleles;
D O I
10.1159/000026195
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
As a part of the WHO Age-Associated Dementia Project, Chile has been participating in a cross-national survey on dementia frequency and determinants since 1989. In the present study, apolipoprotein E (ApoE) polymorphism genotypes have been compared in 95 patients with Alzheimer's disease (AD) (mean age 80.7; 95% CI 79.2-82.2, range 66-97) and 187 healthy people (mean age 78.2; 95% CI 77.2-79.2, range 65-93). Isoelectric focusing and immunoblotting with anti-human ApoE polyclonal antibody were used to determine the distribution of ApoE genotypes. Dementia was diagnosed according to DSM-III-R and ICD-10 clinical criteria. The diagnosis of probable or possible AD was made according to the NINCDS-ADRDA criteria. The ApoE allele frequencies in healthy people were calculated to be epsilon 2 = 0.07, epsilon 3 = 0.74 and epsilon 4 = 0.19. In the probable AD disease group, the frequencies were epsilon 2 = 0.08, epsilon 3 = 0.52 and epsilon 4 = 0.40. The odds ratio (OR) for epsilon 4 carriers compared with non-epsilon 4 carriers was estimated to be 2.9 (95% CI 1.7-5.1). Taking the genotype epsilon 3/epsilon 3 as the reference group, the OR for the epsilon 4/epsilon 4 genotype was estimated to be 12.8 (95% CI 3.9-47.6) and for epsilon 3/epsilon 4 subjects it was 2.4 (1.3-4.5). These results support the association between ApoE epsilon 4 allele with late-onset AD in a Chilean population.
引用
收藏
页码:48 / 52
页数:5
相关论文
共 21 条
[1]  
Amaducci L, 1991, Aging (Milano), V3, P89
[2]  
[Anonymous], 1987, DIAGNOSTIC STAT MANU, V4th
[3]   MULTIPLE SIGNIFICANCE TESTS - THE BONFERRONI METHOD .10. [J].
BLAND, JM ;
ALTMAN, DG .
BRITISH MEDICAL JOURNAL, 1995, 310 (6973) :170-170
[4]   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
[5]   PERFORMING THE EXACT TEST OF HARDY-WEINBERG PROPORTION FOR MULTIPLE ALLELES [J].
GUO, SW ;
THOMPSON, EA .
BIOMETRICS, 1992, 48 (02) :361-372
[6]   GENETIC DISSECTION OF COMPLEX TRAITS [J].
LANDER, ES ;
SCHORK, NJ .
SCIENCE, 1994, 265 (5181) :2037-2048
[7]   ASSOCIATION OF APOLIPOPROTEIN-E ALLELE EPSILON-4 WITH LATE-ONSET SPORADIC ALZHEIMERS-DISEASE [J].
LUCOTTE, G ;
VISVIKIS, S ;
LEININGERMULER, B ;
DAVID, F ;
BERRICHE, S ;
REVEILLEAU, S ;
COUDERC, R ;
BABRON, MC ;
AGUILLON, D ;
SIEST, G .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 54 (03) :286-288
[8]  
MCDOWELL IFW, 1989, CLIN CHEM, V35, P2070
[9]  
MCKHANN G, 1984, NEUROLOGY, V34, P939, DOI 10.1212/WNL.34.7.939
[10]   COMPUTING AN EXACT CONFIDENCE-INTERVAL FOR THE COMMON ODDS RATIO IN SEVERAL 2X2 CONTINGENCY-TABLES [J].
MEHTA, CR ;
PATEL, NR ;
GRAY, R .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1985, 80 (392) :969-973