Literature DB >> 8111623

The cortical topography of temporal lobe hypometabolism in early Alzheimer's disease.

W J Jagust1, J L Eberling, B C Richardson, B R Reed, M G Baker, T E Nordahl, T F Budinger.   

Abstract

Alzheimer's disease (AD) is characterized by a pathological process with specific predilection for association neocortex and the mesial temporal lobes. Recently developed high-resolution positron emission tomographs (PET) are able to quantitate regional cerebral metabolic rates for glucose (rCMRglc) in these brain regions and map the distribution of the metabolic consequences of Alzheimer pathology. In order to evaluate the relative involvement of mesial and neocortical temporal lobe brain regions in AD, we studied 22 AD patients, 11 of whom were mildly demented and 11 of whom were moderately demented in comparison to 8 age-matched control subjects. We used a PET instrument with 2.6 mm in-plane resolution and quantitated rCMRglc in anterior, middle, and posterior temporal neocortex, visual association cortex, primary visual cortex, and mesial temporal cortex. Although the moderately demented AD patients showed significantly lower metabolic rates than controls in visual association cortex and all temporal lobe regions except right anterior temporal neocortex, the mildly demented patients were different from the controls in only middle temporal neocortex. Considerable variability was found in the relative involvement of mesial temporal lobes and temporal neocortex in the AD patients, however, as shown by greater variance of a ratio of mesial temporal lobe rCMRglc to temporal neocortical rCMRglc (MES/NEO ratio) in the AD patients than the controls. A series of stepwise multiple regressions showed that this ratio was related to patient cognitive symptomatology, with more severely memory-impaired patients showing lower MES/NEO ratios, while patients with visuospatial disturbances showed higher MES/NEO ratios. In addition, the only biological variable that was related to this ratio was patient age, with older patients showing lower MES/NEO ratios. These results indicate that mesial temporal lobe structures are not invariably the earliest nor the most severely metabolically involved brain regions in AD and that the relative involvement of the mesial and neocortical temporal lobe is related to the patient's cognitive symptoms and age.

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Year:  1993        PMID: 8111623     DOI: 10.1016/0006-8993(93)91320-r

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  11 in total

1.  Method to correlate 1H MRSI and 18FDG-PET.

Authors:  J O'Neill; J L Eberling; N Schuff; W Jagust; B Reed; G Soto; F Ezekiel; G Klein; M W Weiner
Journal:  Magn Reson Med       Date:  2000-02       Impact factor: 4.668

2.  Effects of subcortical cerebral infarction on cortical glucose metabolism and cognitive function.

Authors:  L T Kwan; B R Reed; J L Eberling; N Schuff; J Tanabe; D Norman; M W Weiner; W J Jagust
Journal:  Arch Neurol       Date:  1999-07

3.  Relations between hypometabolism in the posterior association neocortex and hippocampal atrophy in Alzheimer's disease: a PET/MRI correlative study.

Authors:  K Meguro; C LeMestric; B Landeau; B Desgranges; F Eustache; J C Baron
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-09       Impact factor: 10.154

4.  Neuropsychology of memory and SPECT in the diagnosis and staging of dementia of Alzheimer type.

Authors:  J D Greene; K Miles; J R Hodges
Journal:  J Neurol       Date:  1996-02       Impact factor: 4.849

Review 5.  Arterial spin labeling blood flow MRI: its role in the early characterization of Alzheimer's disease.

Authors:  David C Alsop; Weiying Dai; Murray Grossman; John A Detre
Journal:  J Alzheimers Dis       Date:  2010       Impact factor: 4.472

Review 6.  Brain glucose metabolism in the early and specific diagnosis of Alzheimer's disease. FDG-PET studies in MCI and AD.

Authors:  Lisa Mosconi
Journal:  Eur J Nucl Med Mol Imaging       Date:  2005-04       Impact factor: 9.236

Review 7.  Dysfunctional Sensory Modalities, Locus Coeruleus, and Basal Forebrain: Early Determinants that Promote Neuropathogenesis of Cognitive and Memory Decline and Alzheimer's Disease.

Authors:  Mak Adam Daulatzai
Journal:  Neurotox Res       Date:  2016-06-23       Impact factor: 3.911

8.  Hippocampal hyperperfusion in Alzheimer's disease.

Authors:  David C Alsop; Melynda Casement; Cedric de Bazelaire; Tamara Fong; Daniel Z Press
Journal:  Neuroimage       Date:  2008-06-17       Impact factor: 6.556

9.  Increased Contact System Activation in Mild Cognitive Impairment Patients with Impaired Short-Term Memory.

Authors:  Pradeep K Singh; Zu-Lin Chen; Sidney Strickland; Erin H Norris
Journal:  J Alzheimers Dis       Date:  2020       Impact factor: 4.472

10.  Alzheimer's disease alters oligodendrocytic glycolytic and ketolytic gene expression.

Authors:  Erin R Saito; Justin B Miller; Oscar Harari; Carlos Cruchaga; Kathie A Mihindukulasuriya; John S K Kauwe; Benjamin T Bikman
Journal:  Alzheimers Dement       Date:  2021-03-02       Impact factor: 21.566

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