Patterns of brain activation in people at risk for Alzheimer's disease

被引:994
作者
Bookheimer, SY
Strojwas, MH
Cohen, MS
Saunders, AM
Pericak-Vance, MA
Mazziotta, JC
Small, GW
机构
[1] Univ Calif Los Angeles, Inst Neuropsychiat, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Dept Neurol, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Dept Radiol, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Dept Mol & Mol Pharmacol, Los Angeles, CA 90024 USA
[5] Univ Calif Los Angeles, Brain Mapping Ctr, Los Angeles, CA 90024 USA
[6] Univ Calif Los Angeles, Alzheimers Dis Res Ctr, Los Angeles, CA 90024 USA
[7] Univ Calif Los Angeles, Ctr Aging, Los Angeles, CA 90024 USA
[8] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[9] Vet Affairs Greater Los Angeles Healthcare Syst, Los Angeles, CA USA
关键词
D O I
10.1056/NEJM200008173430701
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The epsilon 4 allele of the apolipoprotein E gene (APOE) is the chief known genetic risk factor for Alzheimer's disease, the most common cause of dementia late in life. To determine the relation between brain responses to tasks requiring memory and the genetic risk of Alzheimer's disease, we performed APOE genotyping and functional magnetic resonance imaging (MRI) of the brain in older persons with intact cognition. Methods: We studied 30 subjects (age, 47 to 82 years) who were neurologically normal, of whom 16 were carriers of the APOE epsilon 4 allele and 14 were homozygous for the APOE epsilon 3 allele. The mean age and level of education were similar in the two groups. Patterns of brain activation during functional MRI scanning were determined while subjects memorized and recalled unrelated pairs of words and while subjects rested between such periods. Memory was reassessed in 14 subjects two years later. Results: Both the magnitude and the extent of brain activation during memory-activation tasks in regions affected by Alzheimer's disease, including the left hippocampal, parietal, and prefrontal regions, were greater among the carriers of the APOE epsilon 4 allele than among the carriers of the APOE epsilon 3 allele. During periods of recall, the carriers of the APOE epsilon 4 allele had a greater average increase in signal intensity in the hippocampal region (1.03 percent vs. 0.62 percent, P<0.001) and a greater mean (+/-SD) number of activated regions throughout the brain (15.9+/-6.2 vs. 9.4+/-5.5, P = 0.005) than did carriers of the APOE epsilon 3 allele. Longitudinal assessment after two years indicated that the degree of base-line brain activation correlated with degree of decline in memory. Conclusions: Patterns of brain activation during tasks requiring memory differ depending on the genetic risk of Alzheimer's disease and may predict a subsequent decline in memory. (N Engl J Med 2000;343:450-6.) (C)2000, Massachusetts Medical Society.
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收藏
页码:450 / 456
页数:7
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