Preclinical evidence of Alzheimer's disease in persons homozygous for the epsilon 4 allele for apolipoprotein E

被引:1085
|
作者
Reiman, EM
Caselli, RJ
Yun, LS
Chen, KW
Bandy, D
Minoshima, S
Thibodeau, SN
Osborne, D
机构
[1] UNIV ARIZONA, DEPT PSYCHIAT, TUCSON, AZ USA
[2] UNIV ARIZONA, DEPT RADIOL, TUCSON, AZ 85724 USA
[3] MAYO CLIN, DEPT NEUROL, SCOTTSDALE, AZ USA
[4] MAYO CLIN, DEPT PSYCHOL, SCOTTSDALE, AZ USA
[5] ARIZONA STATE UNIV, DEPT COMP SCI, TEMPE, AZ 85287 USA
[6] UNIV MICHIGAN, DIV NUCL MED, ANN ARBOR, MI 48109 USA
[7] MAYO CLIN, DEPT LAB MED & PATHOL, ROCHESTER, MN USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 1996年 / 334卷 / 12期
关键词
D O I
10.1056/NEJM199603213341202
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Variants of the apolipoprotein pared regional rates of glucose metabolism in the two groups. E allele appear to account for most cases of late-onset Alzheimer's disease, and persons with two copies of the epsilon 4 allele appear to have an especially high risk of dementia. Positron-emission tomography (PET) has identified specific regions of the brain In which the rate of glucose metabolism declines progressively in patients with probable Alzheimer's disease, We used PET to investigate whether these same regions of the brain are affected in subjects homozygous for the epsilon 4 allele before the onset of cognitive impairment. Methods. Apolipoprotein E genotypes were established in 235 volunteers 50 to 65 years of age who reported a family history of probable Alzheimer's disease, Neurologic and psychiatric evaluations, a battery of neuropsychological tests, magnetic resonance imaging, and PET were performed in 11 E4 homozygotes and 22 controls without the epsilon 4 allele who were matched for sex, age, and level of education. An automated method was used to generate an aggregate surface-projection map that compared regional rates of glucose metabolism in the two groups. Results. The epsilon 4 homozygotes were cognitively normal, They had significantly reduced rates of glucose metabolism In the same posterior cingulate, parietal, temporal, and prefrontal regions as in previously studied patients with probable Alzheimer's disease, They also had reduced rates of glucose metabolism in additional prefrontal regions, which may be preferentially affected during normal aging. Conclusions. In late middle age, cognitively normal subjects who are homozygous for the epsilon 4 allele for apolipoprotein E have reduced glucose metabolism in the same regions of the brain as in patients with probable Alzheimer's disease, These findings provide preclinical evidence that the presence of the epsilon 4 allele is a risk factor for Alzheimer's disease, PET may offer a relatively rapid way of testing future treatments to prevent Alzheimer's disease. (C) 1996, Massachusetts Medical Society.
引用
收藏
页码:752 / 758
页数:7
相关论文
共 50 条
  • [21] Association of apolipoprotein E epsilon 4 allele with sporadic late onset Alzheimer's disease A meta-analysis
    Sadigh-Eteghad, Saeed
    Talebi, Mahnaz
    Farhoudi, Mehdi
    NEUROSCIENCES, 2012, 17 (03) : 321 - 326
  • [22] Clinical and pathological correlates of apolipoprotein E epsilon 4 in Alzheimer's disease
    GomezIsla, T
    West, HL
    Rebeck, GW
    Harr, SD
    Growdon, JH
    Locascio, JJ
    Perls, TT
    Lipsitz, LA
    Hyman, BT
    ANNALS OF NEUROLOGY, 1996, 39 (01) : 62 - 70
  • [23] The frequency of apolipoprotein epsilon 4 allele in Alzheimer's disease and non-demented elderly
    Ocic, G
    Smiljkovic, P
    Pavlovic, D
    Zugic, S
    Golubovic, S
    Smiljkovic, T
    NEUROBIOLOGY OF AGING, 2002, 23 (01) : S285 - S286
  • [24] The absence of an apolipoprotein epsilon 4 allele is associated with a more aggressive form of Alzheimer's disease
    Stern, Y
    Brandt, J
    Albert, M
    Jacobs, DM
    Liu, XH
    Bell, K
    Marder, K
    Sano, M
    Albert, S
    Castenada, CD
    Bylsma, F
    Tycko, B
    Mayeux, R
    ANNALS OF NEUROLOGY, 1997, 41 (05) : 615 - 620
  • [25] Apolipoprotein E epsilon 4 allele and schizophrenia
    Kimura, T
    Yokota, S
    Shono, M
    IgataYi, R
    Takamatsu, J
    Miyakawa, T
    NEUROREPORT, 1997, 8 (17) : R1 - R2
  • [26] Serum total cholesterol, apolipoprotein E ε4 allele, and Alzheimer's disease
    Notkola, IL
    Sulkava, R
    Pekkanen, J
    Erkinjuntti, T
    Ehnholm, C
    Kivinen, P
    Tuomilehto, A
    Nissinen, A
    NEUROEPIDEMIOLOGY, 1998, 17 (01) : 14 - 20
  • [27] The apolipoprotein E ε4 allele and the response to tacrine therapy in Alzheimer's disease
    Rigaud, AS
    Traykov, L
    Caputo, L
    Guelfi, MC
    Latour, F
    Couderc, R
    Moulin, F
    de Rotrou, J
    Forette, F
    Boller, F
    EUROPEAN JOURNAL OF NEUROLOGY, 2000, 7 (03) : 255 - 258
  • [28] Apolipoprotein E ε4 allele frequency and age at onset of Alzheimer's disease
    Davidson, Yvonne
    Gibbons, Linda
    Pritchard, Antonia
    Hardicre, Jayne
    Wren, Joanne
    Stopford, Cheryl
    Julien, Camille
    Thompson, Jennifer
    Payton, Antony
    Pickering-Brown, Stuart M.
    Pendleton, Neil
    Horan, Michael A.
    Burns, Alistair
    Purandare, Nitin
    Lendon, Corinne L.
    Neary, David
    Snowden, Julie S.
    Mann, David M. A.
    DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2007, 23 (01) : 60 - 66
  • [29] Accelerated hippocampal atrophy in Alzheimer's disease with apolipoprotein E ε4 allele
    Mori, E
    Lee, K
    Yasuda, M
    Hashimoto, M
    Kazui, H
    Hirono, H
    Matsui, M
    ANNALS OF NEUROLOGY, 2002, 51 (02) : 209 - 214
  • [30] Apolipoprotein E4 allele and ribosomal genes in Alzheimer's disease
    Tavares, WM
    Sperança, MA
    de Labio, RW
    Peres, CA
    Okamoto, IH
    Bertolucci, PHF
    Smith, MD
    Payao, SLM
    JOURNAL OF ALZHEIMERS DISEASE, 2004, 6 (04) : 391 - 395