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December 23, 2003; 61 (12) Articles

Temporal cortex hypermetabolism in Down syndrome prior to the onset of dementia

R. J. Haier, M. T. Alkire, N. S. White, M. R. Uncapher, E. Head, I. T. Lott, C. W. Cotman
First published December 22, 2003, DOI: https://doi.org/10.1212/01.WNL.0000098935.36984.25
R. J. Haier
PhD
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M. T. Alkire
MD
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N. S. White
BS
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M. R. Uncapher
BS
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E. Head
PhD
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I. T. Lott
MD
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C. W. Cotman
PhD
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Citation
Temporal cortex hypermetabolism in Down syndrome prior to the onset of dementia
R. J. Haier, M. T. Alkire, N. S. White, M. R. Uncapher, E. Head, I. T. Lott, C. W. Cotman
Neurology Dec 2003, 61 (12) 1673-1679; DOI: 10.1212/01.WNL.0000098935.36984.25

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Abstract

Background: Adults with Down syndrome (DS) are at increased risk for dementia and provide an opportunity to identify patterns of brain activity that may precede dementia. Studies of early Alzheimer’s disease (AD) and risk of AD show decreased function in posterior cingulate and temporal cortex as initial indicators of the disease process, but whether the origin and sequence of predementia brain changes are the same in DS is unknown.

Methods: The regional cerebral glucose metabolic rates (GMR) among middle-aged nondemented people with DS (n = 17), people with moderate AD (n = 10), and age-matched control subjects (n = 24) were compared using PET during a cognitive task.

Results: Statistical parametric mapping conjunction analyses showed that 1) both DS and AD groups had lower GMR than their respective controls primarily in posterior cingulate and 2) compared with respective controls, the subjects with DS had higher GMR in the same areas of inferior temporal/entorhinal cortex where the AD subjects had lower GMR. The same results were replicated after 1 year of follow-up.

Conclusions: As the DS subjects were not clinically demented, inferior temporal/entorhinal cortex hypermetabolism may reflect a compensatory response early in disease progression. Compensatory responses may subsequently fail, leading to neurodegenerative processes that the authors anticipate will be detectable in vivo as future GMR decreases in inferior temporal/entorhinal cortex are accompanied by clinical signs of dementia.

  • Received May 27, 2003.
  • Accepted September 8, 2003.
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