Journal of the Neurological Sciences
Volume 200, Issue 1 , Pages 27-32, 15 August 2002

Differences in cerebral metabolic impairment between early and late onset types of Alzheimer's disease

  • Setsu Sakamoto

      Affiliations

    • Division of Imaging Research, Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), 520 Saisho-Ko Himeji, Hyogo 670-0981, Japan
  • ,
  • Kazunari Ishii

      Affiliations

    • Corresponding Author InformationCorresponding author. Division of Imaging Research, Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), 520 Saisho-Ko, Himeji, Hyogo 670-0981, Japan. Tel.: +81-792-95-5511; fax: +81-792-95-8199
    • Division of Imaging Research, Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), 520 Saisho-Ko Himeji, Hyogo 670-0981, Japan
  • ,
  • Masahiro Sasaki

      Affiliations

    • Division of Imaging Research, Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), 520 Saisho-Ko Himeji, Hyogo 670-0981, Japan
  • ,
  • Kayo Hosaka

      Affiliations

    • Division of Imaging Research, Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), 520 Saisho-Ko Himeji, Hyogo 670-0981, Japan
    • Department of Radiology, Kobe University School of Medicine, Kobe, Hyogo, Japan
  • ,
  • Tetsuya Mori

      Affiliations

    • Division of Imaging Research, Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), 520 Saisho-Ko Himeji, Hyogo 670-0981, Japan
  • ,
  • Mieko Matsui

      Affiliations

    • Division of Imaging Research, Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), 520 Saisho-Ko Himeji, Hyogo 670-0981, Japan
  • ,
  • Nobutsugu Hirono

      Affiliations

    • Division of Neurosciences,Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Hyogo, Japan
  • ,
  • Etsuro Mori

      Affiliations

    • Division of Neurosciences,Hyogo Institute for Aging Brain and Cognitive Disorders (HI-ABCD), Himeji, Hyogo, Japan

Received 5 February 2002; received in revised form 19 April 2002; accepted 22 April 2002.

Abstract 

The purpose of this study was to delineate the specific patterns of cerebral glucose metabolism with regard to the time of onset of Alzheimer's disease (AD). Methods: Two groups of 20 AD patients with different ages of onset were examined. The early onset (EO) and late onset (LO) groups had mean ages of onset of 53.9 and 72.7 years. Groups of age-matched normal subjects were used as controls. A regional relative cerebral glucose metabolic image of each subject was obtained by 2-[18F] fluoro-2-deoxy-d-glucose (FDG) positron emission tomography (PET). NEUROSTAT program was used for spatial normalization and voxel-based statistical parametric mapping (SPM) 99 was used for statistical analyses. Results: Both AD groups had significant hypometabolic regions in the bilateral parieto-temporal regions compared with the age-matched groups. The EO group had more severe hypometabolism in the bilateral parietal and posterior cingulate cortices and precuneus region than the LO group. However, LO group showed no significant hypometabolic regions compared to the EO group. Conclusion: The effects of time of AD onset were delineated as a double dissociation, that is, EO AD patients have a more severe reduction of glucose metabolism. Our finding suggests the existence of biological subtypes of AD.

Keywords:  Alzheimer's disease, Age, PET, Glucose metabolism, Voxel-by-voxel statistics

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0022-510X(02)00114-4

Journal of the Neurological Sciences
Volume 200, Issue 1 , Pages 27-32, 15 August 2002