Brain stem serotonin-synthesizing neurons in Alzheimer's disease: a clinicopathological correlation

Acta Neuropathol. 1992;84(6):638-50. doi: 10.1007/BF00227741.

Abstract

The location and number of brain stem serotonin-synthesizing neurons were analyzed in 11 patients with Alzheimer's disease (AD) and 5 age-matched controls using immunohistochemical techniques. In addition, the number of neuritic plaques and neurofibrillary tangles in the cortex and brain stem raphe was evaluated, as was the number of Nissl-stained raphe neurons. AD patients could be classified into two groups based on their raphe pathology; patients with such pathology (AD+) and those without (AD-). The number of large raphe neurons correlated significantly with the number of serotonin-synthesizing neurons in control material, indicating that all large neurons were serotonergic. This relationship was not apparent in AD+ patients, in whom the number of serotonin-synthesizing neurons correlated with the number of neurofibrillary tangles in the raphe of these patients. This indicates that in AD+ patients the serotonin-synthesizing neurons were selectively affected. There was no correlation between raphe and cortical pathology or raphe pathology and patient sex, age, mini-mental score or depression score, even when such scores were weighted for the interval between testing and death. There was a trend for the raphe pathology to correlate with the age of onset and duration of dementia and the Blessed dementia score in AD+ patients. Most AD+ patients with severe raphe lesions had clinical dementia only, while AD- patients had additional clinical features. The raphe lesions were more dramatic in AD+ patients with a rapid progression of symptoms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / metabolism*
  • Alzheimer Disease / pathology
  • Alzheimer Disease / psychology
  • Brain Stem / cytology
  • Brain Stem / metabolism*
  • Brain Stem / pathology
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / pathology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neurofibrillary Tangles / pathology
  • Neurons / metabolism*
  • Psychiatric Status Rating Scales
  • Raphe Nuclei / metabolism
  • Raphe Nuclei / pathology
  • Serotonin / biosynthesis*
  • Staining and Labeling

Substances

  • Serotonin