The genetics of Alzheimer disease - Current status and future prospects

被引:136
作者
Blacker, D
Tanzi, RE
机构
[1] Massachusetts Gen Hosp, Dept Psychiat, Gerontol Res Unit, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Neurol, Genet & Aging Unit, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
关键词
D O I
10.1001/archneur.55.3.294
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Four genes involved in the development of Alzheimer disease have been identified. Three fully penetrant (deterministic) genes lead to the development of Alzheimer disease in patients younger than 60 years: the amyloid beta-protein precursor on chromosome 21, presenilin 1 on chromosome 14, and presenilin 2 on chromosome 1. Together, they account for about half of this early-onset form of the disease. One genetic risk factor-apolipoprotein E-4-is associated with late-onset Alzheimer disease. It accounts for a substantial fraction of disease burden but seems to act primarily to lower the age of disease onset. In general, none of these genes can be easily adapted for use as a diagnostic or predictive test for Alzheimer disease. Research activity includes searching for additional genes, especially for late-onset disease, and elucidating the mechanism of action of all identified genes as part of a long-term effort to develop more effective therapeutic and preventive strategies.
引用
收藏
页码:294 / 296
页数:3
相关论文
共 27 条
[11]   QUANTITATIVE-ANALYSIS OF SENILE PLAQUES IN ALZHEIMER-DISEASE - OBSERVATION OF LOG-NORMAL SIZE DISTRIBUTION AND MOLECULAR EPIDEMIOLOGY OF DIFFERENCES ASSOCIATED WITH APOLIPOPROTEIN-E GENOTYPE AND TRISOMY-21 (DOWN-SYNDROME) [J].
HYMAN, BT ;
WEST, HL ;
REBECK, GW ;
BULDYREV, SV ;
MANTEGNA, RN ;
UKLEJA, M ;
HAVLIN, S ;
STANLEY, HE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (08) :3586-3590
[12]   Alternative cleavage of Alzheimer-associated presenilins during apoptosis by a caspase-3 family protease [J].
Kim, TW ;
Pettingell, WH ;
Jung, YK ;
Kovacs, DM ;
Tanzi, RE .
SCIENCE, 1997, 277 (5324) :373-376
[13]   Risk of dementia among relatives of Alzheimer's disease patients in the MIRAGE study: What is in store for the oldest old? [J].
Lautenschlager, NT ;
Cupples, LA ;
Rao, VS ;
Auerbach, SA ;
Becker, R ;
Burke, J ;
Chui, H ;
Duara, R ;
Foley, EJ ;
Glatt, SL ;
Green, RC ;
Jones, R ;
Karlinsky, H ;
Kukull, WA ;
Kurz, A ;
Larson, EB ;
Martelli, K ;
Sadovnick, AD ;
Volicer, L ;
Waring, SC ;
Growdon, JH ;
Farrer, LA .
NEUROLOGY, 1996, 46 (03) :641-650
[14]   CANDIDATE GENE FOR THE CHROMOSOME-1 FAMILIAL ALZHEIMERS-DISEASE LOCUS [J].
LEVYLAHAD, E ;
WASCO, W ;
POORKAJ, P ;
ROMANO, DM ;
OSHIMA, J ;
PETTINGELL, WH ;
YU, CE ;
JONDRO, PD ;
SCHMIDT, SD ;
WANG, K ;
CROWLEY, AC ;
FU, YH ;
GUENETTE, SY ;
GALAS, D ;
NEMENS, E ;
WIJSMAN, EM ;
BIRD, TD ;
SCHELLENBERG, GD ;
TANZI, RE .
SCIENCE, 1995, 269 (5226) :973-977
[15]   APOLIPOPROTEIN-E4 ALLELE AND ALZHEIMERS-DISEASE - EXAMINATION OF ALLELIC ASSOCIATION AND EFFECT ON AGE AT ONSET IN BOTH EARLY-ONSET AND LATE-ONSET CASES [J].
LOCKE, PA ;
CONNEALLY, PM ;
TANZI, RE ;
GUSELLA, JF ;
HAINES, JL .
GENETIC EPIDEMIOLOGY, 1995, 12 (01) :83-92
[16]   Apolipoprotein E genotyping in Alzheimer's disease [J].
Relkin, NR ;
Tanzi, R ;
Breitner, J ;
Farrer, L ;
Gandy, S ;
Haines, J ;
Hyman, B ;
Mullan, M ;
Poirer, J ;
Strittmatter, W ;
Folstein, M ;
Farlow, M ;
Mayeux, R ;
Petersen, R ;
Roses, A ;
Schenk, D ;
Small, G ;
VanGool, W ;
CookDeegan, R ;
Fleck, L ;
Kapp, M ;
Karlinsky, H ;
PericakVance, M ;
Post, S ;
Wolpert, C ;
Berg, L ;
Blass, J ;
Fletcher, J ;
Hegele, R ;
Khachaturian, Z ;
Selkoe, D ;
Thal, L ;
Whitehouse, P ;
Kwon, YG .
LANCET, 1996, 347 (9008) :1091-1095
[17]   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
[18]   GENETIC-LINKAGE EVIDENCE FOR A FAMILIAL ALZHEIMERS-DISEASE LOCUS ON CHROMOSOME-14 [J].
SCHELLENBERG, GD ;
BIRD, TD ;
WIJSMAN, EM ;
ORR, HT ;
ANDERSON, L ;
NEMENS, E ;
WHITE, JA ;
BONNYCASTLE, L ;
WEBER, JL ;
ALONSO, ME ;
POTTER, H ;
HESTON, LL ;
MARTIN, GM .
SCIENCE, 1992, 258 (5082) :668-671
[19]   GENETIC DISSECTION OF ALZHEIMER-DISEASE, A HETEROGENEOUS DISORDER [J].
SCHELLENBERG, GD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (19) :8552-8559
[20]   Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease [J].
Scheuner, D ;
Eckman, C ;
Jensen, M ;
Song, X ;
Citron, M ;
Suzuki, N ;
Bird, TD ;
Hardy, J ;
Hutton, M ;
Kukull, W ;
Larson, E ;
LevyLahad, E ;
Viitanen, M ;
Peskind, E ;
Poorkaj, P ;
Schellenberg, G ;
Tanzi, R ;
Wasco, W ;
Lannfelt, L ;
Selkoe, D ;
Younkin, S .
NATURE MEDICINE, 1996, 2 (08) :864-870