Reversible Alcohol-related Dementia: A Five-year Follow-up Study Using FDG-PET and Neuropsychological Tests

  • Asada Tomohiko
    Human Brain Research Center, Kyoto University Graduate School of Medicine
  • Takaya Shigetoshi
    Human Brain Research Center, Kyoto University Graduate School of Medicine Radioisotope Research Center, Kyoto University
  • Takayama Yoshihiro
    Department of Speech Physiology, Graduate School of Medicine, University of Tokyo
  • Yamauchi Hiroshi
    Human Brain Research Center, Kyoto University Graduate School of Medicine
  • Hashikawa Kazuo
    Human Brain Research Center, Kyoto University Graduate School of Medicine National Hospital Organization, Osaka Minami Medical Center
  • Fukuyama Hidenao
    Human Brain Research Center, Kyoto University Graduate School of Medicine

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Abstract

Objective As the pathophysiology of alcohol-related dementia (ARD) is unclear, we examined a patient with reversible ARD using neuropsychological tests and 18F-fluorodeoxyglucose positron emission tomography (FDG-PET).<br> Methods Design: A five-year follow-up case study with neuropsychological tests and FDG-PET. Setting: Kyoto University Hospital.<br> Patients A 42-year-old patient who was unable to perform his office duties because of slowly progressive amnesia with executive dysfunction.<br> Results The initial evaluation with neuropsychological tests showed severe verbal memory disturbance. The patient did not discuss his excessive alcohol consumption in the initial history-taking session and thiamine deficiency was absent; therefore, early-stage Alzheimer's disease was suspected. Later, the patient revealed prior excessive alcohol intake and his cognitive function improved markedly after a period of abstinence. Retrospective analysis of initial FDG-PET images using a voxel-wise statistical method revealed glucose hypometabolism in the diencephalon and basal forebrain. Follow-up for 5 years after the initial evaluation showed improved cognitive function and recovery of glucose metabolism in the two brain regions.<br> Conclusion Hypofunction in the diencephalon and basal forebrain was associated with cognitive decline in our patient. This case may provide evidence for the etiopathic brain regions in reversible type ARD.<br>

Journal

  • Internal Medicine

    Internal Medicine 49 (4), 283-287, 2010

    The Japanese Society of Internal Medicine

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