Acute response to cholinergic challenge predicts long-term response to galantamine treatment in patients with Alzheimer's disease.


Journal

British journal of clinical pharmacology
ISSN: 1365-2125
Titre abrégé: Br J Clin Pharmacol
Pays: England
ID NLM: 7503323

Informations de publication

Date de publication:
06 2022
Historique:
revised: 30 11 2021
received: 18 06 2021
accepted: 09 12 2021
pubmed: 30 12 2021
medline: 18 5 2022
entrez: 29 12 2021
Statut: ppublish

Résumé

Cholinesterase inhibitors (CEIs) have been shown to improve cognitive functioning in Alzheimer's disease (AD) patients, but are associated with multiple side effects and only 20-40% of the patients clinically improve. In this study, we aimed to investigate the acute pharmacodynamic (PD) effects of administration of a single dose of galantamine on central nervous system (CNS) functioning in mild to moderate AD patients and its potential to predict long-term treatment response. This study consisted of a challenge and treatment phase. In the challenge phase, a single dose of 16 mg galantamine was administered to 50 mild to moderate AD patients in a double-blind, placebo-controlled cross-over fashion. Acute PD effects were monitored up to 5 hours after administration with use of the NeuroCart CNS test battery and safety and pharmacokinetics were assessed. In the treatment phase, patients were treated with open-label galantamine according to regular clinical care. After 6 months of galantamine treatment, patients were categorized as either responder or as non-responder based on their minimental state examination (MMSE), neuropsychiatric inventory (NPI) and disability assessment in dementia (DAD) scores. An analysis of covariance was performed to study the difference in acute PD effects during the challenge phase between responders and non-responders. A single dose of galantamine significantly reduced saccadic reaction time (-0.0099; 95% CI = -0.0195, -0.0003; P = .0430), absolute frontal EEG parameters in alpha (-14.9; 95% CI = -21.0, -8.3; P = .0002), beta (-12.6; 95% CI = -19.4, -5.3; P = .0019) and theta (-17.9; 95% CI = -25.0, -10.0; P = .0001) frequencies. Relative frontal (-1.669; 95% CI = -2.999, -0.339; P = .0156) and occipital (-1.856; 95% CI = -3.339, -0.372; P = .0166) EEG power in theta frequency and relative occipital EEG power in the gamma frequency (1.316; 95% CI = 0.158, 2.475; P = .0273) also increased significantly compared to placebo. Acute decreases of absolute frontal alpha (-20.4; 95% CI = -31.6, -7.47; P = .0046), beta (-15.7; 95% CI = -28.3, -0.93; P = .0390) and theta (-25.9; 95% CI = -38.4, -10.9; P = .0024) EEG parameters and of relative frontal theta power (-3.27%; 95% CI = -5.96, -0.58; P = .0187) on EEG significantly distinguished responders (n = 11) from non-responders (n = 32) after 6 months. This study demonstrates that acute PD effects after single dose of galantamine are correlated with long-term treatment effects and that patients who demonstrate a reduction in EEG power in the alpha and theta frequency after a single administration of galantamine 16 mg will most likely respond to treatment.

Identifiants

pubmed: 34964149
doi: 10.1111/bcp.15206
pmc: PMC9306507
doi:

Substances chimiques

Cholinesterase Inhibitors 0
Nootropic Agents 0
Galantamine 0D3Q044KCA

Banques de données

ISRCTN
['ISRCTN82825745']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2814-2829

Informations de copyright

© 2021 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

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Auteurs

Anne Catrien Baakman (AC)

Centre for Human Drug Research, Leiden, The Netherlands.

Carmen Gavan (C)

Clinicii de neurologie a Spitalului Universitar de Urgenta, Bucharest, Romania.

Lotte van Doeselaar (L)

Centre for Human Drug Research, Leiden, The Netherlands.

Marieke de Kam (M)

Centre for Human Drug Research, Leiden, The Netherlands.

Karen Broekhuizen (K)

Centre for Human Drug Research, Leiden, The Netherlands.

Ovidiu Bajenaru (O)

Clinicii de neurologie a Spitalului Universitar de Urgenta, Bucharest, Romania.

Laura Camps (L)

Centre for Human Drug Research, Leiden, The Netherlands.

Eleonora L Swart (EL)

Department of Clinical Pharmacology and Pharmacy, Amsterdam UMC, Amsterdam, The Netherlands.

Kees Kalisvaart (K)

Department of Neurology, Spaarne Gasthuis, Haarlem, The Netherlands.

Niki Schoonenboom (N)

Department of Neurology, Spaarne Gasthuis, Haarlem, The Netherlands.

Evelien Lemstra (E)

Alzheimer Center Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.

Philip Scheltens (P)

Alzheimer Center Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.

Adam Cohen (A)

Centre for Human Drug Research, Leiden, The Netherlands.

Joop van Gerven (J)

Centre for Human Drug Research, Leiden, The Netherlands.

Geert Jan Groeneveld (GJ)

Centre for Human Drug Research, Leiden, The Netherlands.
Leiden University Medical Center, Leiden, The Netherlands.

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