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July 1, 1998

Regional cerebral glucose metabolism in dementia with Lewy bodies and Alzheimer's disease

July 1998 issue
51 (1) 125-130

Abstract

Objective: To delineate the features of regional cerebral metabolic rate of glucose(CMRglc) in dementia with Lewy bodies (DLB).
Methods: We compared absolute CMRglc in 12 patients with a clinical diagnosis of DLB, 12 patients with a clinical diagnosis of Alzheimer's disease (AD), and 12 normal volunteers (NC), using 18F-fluorodeoxyglucose (FDG) and PET. The three groups were matched for age and sex, and there were no differences in disease duration or severity of cognitive disturbances between the DLB and AD groups.
Results: CMRglc was significantly lower in patients with DLB than in that of NC in most parts of the brain, except the sensorimotor cortices, basal ganglia, thalamus, and pons. Between the DLB and AD groups, there were significant regional CMRglc differences in the medial and lateral occipital lobes. In DLB and AD, the CMRglc reduction patterns were similar, though the global metabolic reduction was larger in DLB, and the occipital CMRglc reduction in DLB could differentiate DLB from AD. The relative occipital CMRglc(normalized to the sensorimotor CMRglc) was a useful measure for the differential diagnosis of DLB from AD. The sensitivity and the specificity were 92% when using the minimal value of the normalized occipital CMRglc in the NC group as the cut-off point.
Conclusion: These different regional CMRglc reductions substantiate the pathologic, neurochemical, and clinical differences between DLB and AD.

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Published In

Neurology®
Volume 51Number 1July 1998
Pages: 125-130
PubMed: 9674790

Publication History

Published online: July 1, 1998
Published in print: July 1998

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Authors

Affiliations & Disclosures

K. Ishii, MD
From the Division of Neuroimaging Research (Drs. Ishii, Sasaki, Yamaji, Sakamoto, and Kitagaki) and the Division of Clinical Neurosciences (Drs. Imamura, Hashimoto, Hirono, Shimomura, and Mori), Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Japan.
T. Imamura, MD
From the Division of Neuroimaging Research (Drs. Ishii, Sasaki, Yamaji, Sakamoto, and Kitagaki) and the Division of Clinical Neurosciences (Drs. Imamura, Hashimoto, Hirono, Shimomura, and Mori), Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Japan.
M. Sasaki, PhD
From the Division of Neuroimaging Research (Drs. Ishii, Sasaki, Yamaji, Sakamoto, and Kitagaki) and the Division of Clinical Neurosciences (Drs. Imamura, Hashimoto, Hirono, Shimomura, and Mori), Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Japan.
S. Yamaji, MD
From the Division of Neuroimaging Research (Drs. Ishii, Sasaki, Yamaji, Sakamoto, and Kitagaki) and the Division of Clinical Neurosciences (Drs. Imamura, Hashimoto, Hirono, Shimomura, and Mori), Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Japan.
S. Sakamoto, MD
From the Division of Neuroimaging Research (Drs. Ishii, Sasaki, Yamaji, Sakamoto, and Kitagaki) and the Division of Clinical Neurosciences (Drs. Imamura, Hashimoto, Hirono, Shimomura, and Mori), Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Japan.
H. Kitagaki, MD
From the Division of Neuroimaging Research (Drs. Ishii, Sasaki, Yamaji, Sakamoto, and Kitagaki) and the Division of Clinical Neurosciences (Drs. Imamura, Hashimoto, Hirono, Shimomura, and Mori), Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Japan.
M. Hashimoto, MD
From the Division of Neuroimaging Research (Drs. Ishii, Sasaki, Yamaji, Sakamoto, and Kitagaki) and the Division of Clinical Neurosciences (Drs. Imamura, Hashimoto, Hirono, Shimomura, and Mori), Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Japan.
N. Hirono, MD
From the Division of Neuroimaging Research (Drs. Ishii, Sasaki, Yamaji, Sakamoto, and Kitagaki) and the Division of Clinical Neurosciences (Drs. Imamura, Hashimoto, Hirono, Shimomura, and Mori), Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Japan.
T. Shimomura, MD
From the Division of Neuroimaging Research (Drs. Ishii, Sasaki, Yamaji, Sakamoto, and Kitagaki) and the Division of Clinical Neurosciences (Drs. Imamura, Hashimoto, Hirono, Shimomura, and Mori), Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Japan.
E. Mori, MD
From the Division of Neuroimaging Research (Drs. Ishii, Sasaki, Yamaji, Sakamoto, and Kitagaki) and the Division of Clinical Neurosciences (Drs. Imamura, Hashimoto, Hirono, Shimomura, and Mori), Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Japan.

Notes

Address correspondence and reprint requests to Dr. Ishii, Division of Neuroimaging Research, Hyogo Institute for Aging Brain and Cognitive Disorders, 520, Saisho-ko, Himeji 670-0981, Japan.

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