QUANTITATIVE-ANALYSIS OF PET AND MRI DATA IN NORMAL AGING AND ALZHEIMERS-DISEASE - ATROPHY WEIGHTED TOTAL BRAIN METABOLISM AND ABSOLUTE WHOLE-BRAIN METABOLISM AS RELIABLE DISCRIMINATORS
A. Alavi et al., QUANTITATIVE-ANALYSIS OF PET AND MRI DATA IN NORMAL AGING AND ALZHEIMERS-DISEASE - ATROPHY WEIGHTED TOTAL BRAIN METABOLISM AND ABSOLUTE WHOLE-BRAIN METABOLISM AS RELIABLE DISCRIMINATORS, The Journal of nuclear medicine, 34(10), 1993, pp. 1681-1687
Average whole brain metabolic rates, when corrected for brain atrophy,
are similar between patients with Alzheimer's disease (AD) and age-ma
tched controls. To elucidate the relationship between reduced cognitiv
e function and cerebral metabolism in patients with AD, we hypothesize
d that the absolute amount of glucose used by the entire brain may pro
ve to be a more reliable indicator of the disease than metabolic rates
calculated for a unit of brain weight. Twenty patients with the proba
ble diagnosis of AD and 17 similarly aged controls underwent F-18-fluo
rodeoxyglucose positron emission tomography (FDG-PET) studies as well
as magnetic resonance imaging (MRI) within a few days of each other. A
verage metabolic rates, when corrected for atrophy, were 3.91 +/- 1.02
and 4.43 +/- 0.87 (mg of glucose per 1 00 cc brain tissue per min +/-
s.d.) respectively for AD patients and controls. Two other indices we
re determined, atrophy weighted total brain metabolism (calculated by
multiplying the brain volume, determined by MR analysis, by the averag
e metabolic rate) and absolute whole brain metabolism (calculated by m
ultiplying the brain volume by the average metabolic rate corrected fo
r atrophy). The former showed a very significant difference between th
e two groups (29.96 +/- 7.90 for AD patients compared to 39.1 +/- 7.0
for controls, p < 0.001). Atrophy weighted total brain metabolism also
correlated very well with mini mental status exam (MMSE) scores (r =
0.59, p < 0.01). Absolute whole brain metabolism was significantly dif
ferent between AD and control groups and correlated well with MMSE. Th
ese data demonstrate that although the metabolic rate per unit weight
of the brain is unchanged in AD compared to controls, atrophy weighted
total brain metabolism and absolute whole brain metabolism are signif
icantly affected. Both indices may prove to be a sensitive correlate f
or cognitive dysfunction in AD.