Seminars in Nuclear Medicine
Volume 38, Issue 4 , Pages 251-261, July 2008

Positron Emission Tomography Scans Obtained for the Evaluation of Cognitive Dysfunction

  • Daniel H.S. Silverman, MD, PhD

      Affiliations

    • David Geffen School of Medicine, University of California, Los Angeles, CA.
    • Corresponding Author InformationAddress reprint requests to Daniel H.S. Silverman, MD, PhD, Nuclear Medicine Clinic, CHS AR-144, UCLA School of Medicine, MC694215, Los Angeles, CA 90095-6942.
  • ,
  • Lisa Mosconi, PhD

      Affiliations

    • New York University School of Medicine, New York, NY.
  • ,
  • Linda Ercoli, PhD

      Affiliations

    • David Geffen School of Medicine, University of California, Los Angeles, CA.
  • ,
  • Wei Chen, MD, PhD

      Affiliations

    • David Geffen School of Medicine, University of California, Los Angeles, CA.
    • Kaiser Permanente of Southern California, Woodland Hills, CA.
  • ,
  • Gary W. Small, MD

      Affiliations

    • David Geffen School of Medicine, University of California, Los Angeles, CA.

The degree of intactness of human cognitive functioning for a given individual spans a wide spectrum, ranging from normal to severely demented. The differential diagnosis for the causes of impairment along that spectrum is also wide, and often difficult to distinguish clinically, which has led to an increasing role for neuroimaging tools in that evaluation. The most frequent causes of dementia are neurodegenerative disorders, Alzheimer's disease being the most prevalent among them, and they produce significant alterations in brain metabolism, with devastating neuropathologic, clinical, social, and economic consequences. These alterations are detectable through positron emission tomography (PET), even in their earliest stages. The most commonly performed PET studies of the brain are performed with 18F-fluorodeoxyglucose as the imaged radiopharmaceutical. Such scans have demonstrated diagnostic and prognostic utility for clinicians evaluating patients with cognitive impairment and in distinguishing among primary neurodegenerative disorders and other etiologies contributing to cognitive decline. In addition to focusing on the effects on cerebral metabolism examined with 18F-fluorodeoxyglucose PET, some other changes occurring in the brains of cognitively impaired patients assessable with other radiotracers will be considered. As preventive and disease-modifying treatments are developed, early detection of accurately diagnosed disease processes facilitated by the use of PET has the potential to substantially impact on the enormous human toll exacted by these diseases.

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PII: S0001-2998(08)00029-9

doi:10.1053/j.semnuclmed.2008.02.006

Seminars in Nuclear Medicine
Volume 38, Issue 4 , Pages 251-261, July 2008