Neurobiology of Aging
Volume 27, Issue 10 , Pages 1372-1384, October 2006

Hippocampal synaptic loss in early Alzheimer's disease and mild cognitive impairment

  • Stephen W. Scheff

      Affiliations

    • Sanders-Brown Center on Aging and the Alzheimer's Disease Research Center, University of Kentucky College of Medicine, 101 Sanders-Brown, Lexington, KY 40536-0230, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1 859 257 1412x270; fax: +1 859 323 2866.
  • ,
  • Douglas A. Price

      Affiliations

    • Sanders-Brown Center on Aging and the Alzheimer's Disease Research Center, University of Kentucky College of Medicine, 101 Sanders-Brown, Lexington, KY 40536-0230, USA
  • ,
  • Frederick A. Schmitt

      Affiliations

    • Sanders-Brown Center on Aging and the Alzheimer's Disease Research Center, University of Kentucky College of Medicine, 101 Sanders-Brown, Lexington, KY 40536-0230, USA
  • ,
  • Elliott J. Mufson

      Affiliations

    • Department of Neurological Sciences and Alzheimer's Disease Center, Rush University Medical Center, Chicago, IL, USA

Received 24 May 2005; received in revised form 2 September 2005; accepted 9 September 2005. published online 14 November 2005.

Abstract 

One of the major neuropathological findings in the brains of individuals with Alzheimer's disease (AD) is a loss of synaptic contacts in both the neocortex and hippocampus. Here we report, for the first time, an estimate of the total number of synapses in the outer molecular layer (OML) of the human dentate gyrus, in individuals with early Alzheimer's disease (eAD), mild cognitive impairment (MCI), or no cognitive impairment (NCI). An unbiased stereologic sampling scheme coupled with transmission electron microscopy to directly visualize synaptic contacts, was used to estimate the total number of synapses in short postmortem autopsy tissue. Individuals with eAD had significantly fewer synapses than the other two diagnostic groups. Seventy-five percent of the individuals with MCI had synaptic values that were lower than the NCI group mean. The number of synapses showed a significant correlation with the subject's Mini-Mental State score and with cognitive tests involving delayed recall. Synaptic loss showed no relationship to Braak stage or to apoE genotype. The volume of the OML was significantly reduced in eAD compared to the other two diagnositic groups that were not different from each other. These data suggest that a loss of afferents from the entorhinal cortex underlie the synapse loss seen in eAD. This study supports the concept that synapse loss is an early event in the disease process and suggests that MCI may be a transition stage between eAD and NCI with synaptic loss a structural correlate involved in cognitive decline.

Keywords: Aging, Cognition, Memory, Synapse, Limbic system, Hippocampus

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: S0197-4580(05)00283-6

doi:10.1016/j.neurobiolaging.2005.09.012

Neurobiology of Aging
Volume 27, Issue 10 , Pages 1372-1384, October 2006