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

Publication ,  Journal Article
Bookheimer, SY; Strojwas, MH; Cohen, MS; Saunders, AM; Pericak-Vance, MA; Mazziotta, JC; Small, GW
Published in: N Engl J Med
August 17, 2000

BACKGROUND: The epsilon4 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 epsilon4 allele and 14 were homozygous for the APOE epsilon3 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 epsilon4 allele than among the carriers of the APOE epsilon3 allele. During periods of recall, the carriers of the APOE epsilon4 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 epsilon3 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.

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Published In

N Engl J Med

DOI

ISSN

0028-4793

Publication Date

August 17, 2000

Volume

343

Issue

7

Start / End Page

450 / 456

Location

United States

Related Subject Headings

  • Neuropsychological Tests
  • Middle Aged
  • Memory
  • Male
  • Magnetic Resonance Imaging
  • Image Processing, Computer-Assisted
  • Humans
  • Hippocampus
  • Heterozygote
  • General & Internal Medicine
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Bookheimer, S. Y., Strojwas, M. H., Cohen, M. S., Saunders, A. M., Pericak-Vance, M. A., Mazziotta, J. C., & Small, G. W. (2000). Patterns of brain activation in people at risk for Alzheimer's disease. N Engl J Med, 343(7), 450–456. https://doi.org/10.1056/NEJM200008173430701
Bookheimer, S. Y., M. H. Strojwas, M. S. Cohen, A. M. Saunders, M. A. Pericak-Vance, J. C. Mazziotta, and G. W. Small. “Patterns of brain activation in people at risk for Alzheimer's disease.N Engl J Med 343, no. 7 (August 17, 2000): 450–56. https://doi.org/10.1056/NEJM200008173430701.
Bookheimer SY, Strojwas MH, Cohen MS, Saunders AM, Pericak-Vance MA, Mazziotta JC, et al. Patterns of brain activation in people at risk for Alzheimer's disease. N Engl J Med. 2000 Aug 17;343(7):450–6.
Bookheimer, S. Y., et al. “Patterns of brain activation in people at risk for Alzheimer's disease.N Engl J Med, vol. 343, no. 7, Aug. 2000, pp. 450–56. Pubmed, doi:10.1056/NEJM200008173430701.
Bookheimer SY, Strojwas MH, Cohen MS, Saunders AM, Pericak-Vance MA, Mazziotta JC, Small GW. Patterns of brain activation in people at risk for Alzheimer's disease. N Engl J Med. 2000 Aug 17;343(7):450–456.
Journal cover image

Published In

N Engl J Med

DOI

ISSN

0028-4793

Publication Date

August 17, 2000

Volume

343

Issue

7

Start / End Page

450 / 456

Location

United States

Related Subject Headings

  • Neuropsychological Tests
  • Middle Aged
  • Memory
  • Male
  • Magnetic Resonance Imaging
  • Image Processing, Computer-Assisted
  • Humans
  • Hippocampus
  • Heterozygote
  • General & Internal Medicine