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Synapse loss in frontal cortex biopsies in Alzheimer's disease: correlation with cognitive severity

S T DeKosky1, S W Scheff

  • 1Department of Neurology, Lexington Veterans Administration, Medical Center, KY.

Insights

Alzheimer's disease (AD) brains show decreased synapse numbers, but increased synapse size, suggesting early neural plasticity. By end-stage AD, both synapse number and size decline, overwhelming compensatory mechanisms.

Area of Science:

  • Neuroscience
  • Neuropathology
  • Alzheimer's Disease Research

Background:

  • Alzheimer's disease (AD) is characterized by progressive neurodegeneration.
  • Synaptic loss is a key feature of AD neuropathology.
  • Understanding synaptic changes is crucial for developing AD therapies.

Purpose of the Study:

  • To investigate ultrastructural changes in synapses in mild to moderate Alzheimer's disease (AD).
  • To correlate synaptic alterations with cognitive decline and enzyme activity in AD patients.

Main Methods:

  • Ultrastructural analysis of biopsied and autopsied cortical tissue from AD patients and age-matched controls.
  • Quantification of synapse number, size, and synaptic contact area.
  • Measurement of choline acetyltransferase activity.

Main Results:

  • Significant decrease in synapse number in lamina III of Brodmann's area 9 in AD brains compared to controls.
  • Enlargement of mean synaptic apposition length correlated with synapse loss; synapse size increased as density declined.
  • Total synaptic contact area remained stable in biopsied AD patients due to compensatory synapse enlargement.
  • Choline acetyltransferase activity was significantly decreased in AD patients.

Conclusions:

  • Evidence of neural plasticity in early to moderate AD, with synaptic enlargement potentially compensating for numerical loss.
  • In end-stage AD, compensatory mechanisms are exceeded, leading to a decline in both synapse number and synaptic contact area.
  • Synapse loss correlates with cognitive impairment (Mini-Mental State examination scores) in AD patients.

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