Cognitive and metabolic responses to metrifonate therapy in Alzheimer disease

Neuropsychiatry Neuropsychol Behav Neurol. 2001 Jan;14(1):63-8.

Abstract

Objective: The objective of this study was to identify the relation between the cognitive benefit seen with the cholinesterase inhibitor metrifonate and changes in brain metabolism as visualized with [18F]-fluorodeoxyglucose positron emission tomography (FDG-PET).

Background: The regional metabolic correlates of treatment with cholinesterase inhibitors are poorly understood.

Methods: Six patients with mild to moderate Alzheimer disease (AD) were evaluated before and after treatment with the long-lasting cholinesterase inhibitor metrifonate. Patients were given 60 or 80 mg of metrifonate per day (based on weight) for 6 to 12 weeks. Clinical evaluations included the cognitive portion of the Alzheimer's Disease Assessment Scale (ADAS-cog), the Mini-Mental State Examination (MMSE), and the Neuropsychiatric Inventory. Imaging was carried out using FDG-PET. The PET studies, registered to a probabilistic anatomic atlas, were normalized across the group's mean intensity levels and subjected to voxel-by-voxel subtraction of the posttreatment minus pretreatment studies. Subvolume thresholding corrected random lobar noise to produce a three-dimensional functional significance map.

Results: The criteria for cognitive improvement with treatment were met for the MMSE (>2 points improvement from baseline), and the drawing subscale of the ADAS-cog was significantly improved with treatment. The three-dimensional significance map revealed a significant metabolic increase of the dorsolateral frontoparietal network on the left and bilateral temporal cortex with metrifonate treatment.

Conclusion: The clinical benefits observed in AD with cholinesterase inhibitor therapy are associated with a metabolic increase of heteromodal cognitive and medial temporal networks.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / complications
  • Alzheimer Disease / drug therapy*
  • Brain / drug effects
  • Brain / physiology*
  • Cholinesterase Inhibitors / pharmacology*
  • Cognition Disorders / drug therapy*
  • Cognition Disorders / etiology
  • Female
  • Fluorodeoxyglucose F18
  • Humans
  • Male
  • Radiopharmaceuticals
  • Tomography, Emission-Computed
  • Treatment Outcome
  • Trichlorfon / pharmacology*

Substances

  • Cholinesterase Inhibitors
  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18
  • Trichlorfon