Abstract:
Alzheimer disease is a common neurodegenerative disorder
consisting of memory impairment and intellectual function that produces
not only profound disabilities in the patient, but a significant cost to
society as well. The biochemical basis for Alzheimer disease is not
completely understood, but both positron-emission tomography and
single-photon- emission computed tomography provide insights into the in
vivo biochemistry associated with this disease. Both techniques show
characteristic brain abnormalities, which consist of reductions in
temporal-parietal metabolism that progress in severity and extent as the
disease itself shows clinical progression. Such noninvasive biochemical
assays may ultimately prove to be of assistance in clinical management,
and are clearly helpful in understanding the pathophysiologic mechanisms
associated with the production of this disease