Voorspellen van medicatie effect bij Dementie

Method to predict side effects of cholinesterase inhibitors in patients with cellular degenerative and vascular dementia

 

Liza van Eijkc , Erwin R. Grootd , Maritza van Spronsene , Yvonne J. Maase , Daniel Keeserb , Oliver Pogarellb & Hessel J. Engelbregta,b
a Hersencentrum, Amsterdam, The Netherlands
b Ludwig-Maximilian University, Munich, Germany
c VU University, Department of Clinical Neuropsychology, Amsterdam, The Netherlands
d Albert Schweitzer Hospital, Dordrecht, the Netherlands
e Leiden University Faculty of Social Sciences, Leiden, The Netherlands
Mailing address: Department of Clinical Neuropsychology, VU University, De Boelelaan 1105, 1081 HV, Amsterdam, The Netherlands. Correspondence should be addressed to Liza van Eijk; liza@hersencentrum.nl.
  • Received 9 November 2014; Revised 10 May 2015; Accepted 25 May 2015
  • Academic Editor: Stavros Baloyannis


Abstract
This study investigates a method to predict medical outcome of cholinesterase inhibitors in patients with Alzheimer’s disease (AD) and Vascular dementia (VaD). Van Gool predicts that patients with cholinergic deficit symptoms will benefit from treatment whereas patients without will experience side effects because of overstimulation of the cholinergic system. We predicted that AD and VaD patients with a longer RT experience fewer side effects than patients with a faster response and that VaD patients have a longer RT than AD patients. A number of 71 patients with AD or VaD diagnosis were included. A sustained attention task was administered, as well as the MMSE and a questionnaire about side effects. Results indicated that VaD patients with a longer RT reported fewer side effects. Furthermore, patients with VaD had a longer RT than patients with AD. MMSE was negatively correlated with RT in the VaD group. Thus, the performance on the attention task seems associated with suffering from side effects and thus tends to predict medical outcome in VaD, but not in AD. Perhaps this attention task was not sensitive enough to measure cholinergic deficit symptoms in AD patients. Furthermore, different doses of medication might confound the effect for the AD group.

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Method to predict side effects of cholinesterase inhibitors in patients with cellular degenerative and vascular dementia