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PET Scan May Detect Presymptomatic Changes In Alzheimer's Disease
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WESTPORT, Aug 01 (Reuters) - Positron emission tomography (PET) may be able
to detect preclinical changes in brain glucose metabolism in persons at
risk for Alzheimer's disease. Such an early diagnostic test could identify
patients who might benefit most from treatments, once they become
available, to prevent or delay the onset of dementia.

Dr. Pietro P. Pietrini of the National Institute on Aging in Bethesda,
Maryland, and colleagues examined regional cerebral glucose metabolism by
PET in 16 adult nondemented patients with trisomy 21. The researchers point
out that, because such subjects inevitably develop Alzheimer's
neuropathology after the age of 40, they "...provide a unique human model
to investigate the preclinical phases of Alzheimer's disease."

Half the subjects were around 36 years of age and half were older, about
50. At rest, the younger and older patients demonstrated similar patterns
of glucose metabolism in all cerebral regions. During audiovisual
stimulation, however, the investigators found that "...older nondemented
subjects with Down's syndrome have significantly lower rates of regional
cerebral glucose metabolism...than do younger subjects with Down's syndrome."

The parietal and temporal regions showed the greatest differences in
glucose metabolism between the younger and older Down's syndrome patients.
These same regions are "...most vulnerable to Alzheimer's disease
neuropathology and the first to show abnormal brain metabolism in
Alzheimer's disease," the authors explain. Moreover, this pattern suggests
that the decline in glucose metabolism is not attributable to the normal
aging process, because this occurs mainly in the frontal lobes.

Overall, the researcher conclude, the findings suggest that "...abnormal
brain metabolism in subjects at risk for developing dementia can be
revealed before the appearance of nonmemory cognitive decline or clinical
dementia."

Am J Psychiatry 1997;154:000-000.
Copyright 1997 Reuters Limited.
<http://www.reutershealth.com/news/docs/199708/19970801clc.html>
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