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      The spatial patterns of plaques and tangles in Alzheimer's disease do not support the 'cascade hypothesis'.

      Dementia (Basel, Switzerland)
      Aged, Alzheimer Disease, pathology, Amyloid beta-Peptides, metabolism, Brain, Cerebral Cortex, Humans, Intermediate Filaments, Middle Aged, Neurofibrillary Tangles, Silver Staining

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          Abstract

          In Alzheimer's disease (AD), the 'Cascade hypothesis' proposes that the formation of paired helical filaments (PHF) may be casually linked to the deposition of beta/A4 protein. Hence, there should be a close spatial relationship between senile plaques and cellular neurofibrillary tangles in a local region of the brain. In tissue from 6 AD patients, plaques and tangles occurred in clusters and individual clusters were often regularly spaced along the cortical strip. However, the clusters of plaques and tangles were in phase in only 4/32 cortical tissues examined. Hence, the data were not consistent with the 'Cascade hypothesis' that beta/A4 and PHF are directly linked in AD.

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