Cerebral metabolic changes associated with Lyme diseaseNEWBERG, A.; HASSAN, A.; ALAVI, A.Nuclear Medicine Communications: August 2002 - Volume 23 - Issue 8 - p 773-777 Original Papers Buy Abstract Author InformationAuthors There are no positron emission tomography (PET) studies reported in the literature with regards to brain metabolism and function in patients with Lyme disease. These patients frequently present with various neurological symptoms, including memory problems. We used [18F]fluorodeoxyglucose (FDG) PET to determine the metabolic landscape in 23 patients with Lyme disease. Images were evaluated for cortical and subcortical abnormalities by two experienced reviewers blinded to the clinical information. The most striking finding was hypometabolism in the temporal lobes in 17/23 (74%) patients. Of these, 12 had bilateral temporal lobe hypometabolism, two had left temporal lobe, and three had right temporal lobe hypometabolism. Seven of the patients with temporal lobe hypometabolism had diffuse cortical hypometabolism that included the frontal and parietal lobes. Lyme disease appears to have two primary patterns of brain involvement on FDG PET scans, specific temporal lobe hypometabolism or a diffuse cortical hypometabolism. The involvement of the temporal lobes in both patterns is likely associated with the memory disturbances described in many of these patients. Although there was no clear diagnostic pattern, and many of the defects were mild, FDG PET imaging may provide important information regarding the areas of the brain affected in patients with neurological symptoms associated with Lyme disease. Division of Nuclear Medicine, Hospital of the University of Pennsylvania, USA Address all correspondence to Dr Andrew B. Newberg, Division of Nuclear Medicine, Department of Radiology, Hospital of the University of Pennsylvania, 110 Donner Building, 3400 Spruce Street, Philadelphia, PA 19104, USA. e-mail: email@example.com Received 17 January 2002, in revised form 6 March 2002 and accepted 7 March 2002 © 2002 Lippincott Williams & Wilkins, Inc.