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Efficacy and safety of choline alphoscerate (cereton) in patients with parkinson’s disease with cognitive impairments

An open 10-day study in which the therapeutic actions of Cereton were compared with those of piracetam was performed. Cereton was used in 40 patients (experimental group) at a dose of 1000 mg, while piracetam was used in 20 patients at a dose of 2000 mg; both agents were given as intravenous infusions in 200 ml of physiological saline on the background of antiparkinsonism agents. Patients’ status was evaluated using a complex of psychometric scales and neuropsychological tests, along with tools to assess the severity of the main symptoms of parkinsonism, side effects, and quality of life. Use of Cereton produced marked and moderate improvements in the state of cognitive functions more frequently than piracetam (40% and 25%, respectively), while the incidence of deterioration was lower (5% and 15%, p < 0.05). Cereton was very well tolerated by the patients: brief and short-term side effects were seen in only six patients (15%).

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Correspondence to O. S. Levin.

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Translated from Zhurnal Nevrologii i Psikhiatrii imeni S. S. Korsakova, Vol. 109, No. 11, pp. 42–46, November, 2009.

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Levin, O.S., Batukaeva, L.A., Anikina, M.A. et al. Efficacy and safety of choline alphoscerate (cereton) in patients with parkinson’s disease with cognitive impairments. Neurosci Behav Physi 41, 47–51 (2011).

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Key Words

  • Parkinson’s disease
  • cognitive impairments
  • correction
  • Cereton (choline alphoscerate)