An Investigation of Levetiracetam in Alzheimer's Disease (ILiAD): a double-blind, placebo-controlled, randomised crossover proof of concept study.

Anti-seizure medication Cognition Dementia Epilepsy Levetiracetam Pilot Proof of concept Randomised controlled trial Seizure

Journal

Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253

Informations de publication

Date de publication:
31 Jul 2021
Historique:
received: 18 10 2020
accepted: 27 06 2021
entrez: 1 8 2021
pubmed: 2 8 2021
medline: 4 8 2021
Statut: epublish

Résumé

Although Alzheimer's disease affects around 800,000 people in the UK and costs almost £23 billion per year, currently licenced treatments only offer modest benefit at best. Seizures, which are more common in patients with Alzheimer's disease than age matched controls, may contribute to the loss of nerve cells and abnormal brain discharges can disrupt cognition. This aberrant electrical activity may therefore present potentially important drug targets. The anti-seizure medication levetiracetam can reduce abnormal cortical discharges and reverse memory deficits in a mouse model of Alzheimer's disease. Levetiracetam has also been shown to improve memory difficulties in patients with mild cognitive impairment, a precursor to Alzheimer's disease. Clinical use of levetiracetam is well-established in treatment of epilepsy and extensive safety data are available. Levetiracetam thus has the potential to provide safe and efficacious treatment to help with memory difficulties in Alzheimer's disease. The proposed project is a proof of concept study to test whether levetiracetam can help cognitive function in people with dementia. We plan to recruit thirty patients with mild to moderate Alzheimer's disease with no history of previous seizures or other significant co-morbidity. Participants will be allocated to a double-blind placebo-controlled crossover trial that tests levetiracetam against placebo. Standardised scales to assess cognition and a computer-based touchscreen test that we have developed to better detect subtle improvements in hippocampal function will be used to measure changes in memory. All participants will have an electroencephalogram (EEG) at baseline. The primary outcome measure is a change in the computer-based touchscreen cognitive task while secondary outcomes include the effect of levetiracetam on mood, quality of life and modelling of the EEG, including time series measures and feature-based analysis to see whether the effect of levetiracetam can be predicted. The effect of levetiracetam and placebo will be compared within a given patient using the paired t-test and the analysis of covariance adjusting for baseline values. This is the first study to evaluate if an anti-seizure medication can offer meaningful benefit to patients with Alzheimer's disease. If this study demonstrates at least stabilisation of memory function and/or good tolerability, the next step will be to rapidly progress to a larger study to establish whether levetiracetam may be a useful and cost-effective treatment for patients with Alzheimer's disease. ClinicalTrials.gov NCT03489044 . Registered on April 5, 2018.

Sections du résumé

BACKGROUND BACKGROUND
Although Alzheimer's disease affects around 800,000 people in the UK and costs almost £23 billion per year, currently licenced treatments only offer modest benefit at best. Seizures, which are more common in patients with Alzheimer's disease than age matched controls, may contribute to the loss of nerve cells and abnormal brain discharges can disrupt cognition. This aberrant electrical activity may therefore present potentially important drug targets. The anti-seizure medication levetiracetam can reduce abnormal cortical discharges and reverse memory deficits in a mouse model of Alzheimer's disease. Levetiracetam has also been shown to improve memory difficulties in patients with mild cognitive impairment, a precursor to Alzheimer's disease. Clinical use of levetiracetam is well-established in treatment of epilepsy and extensive safety data are available. Levetiracetam thus has the potential to provide safe and efficacious treatment to help with memory difficulties in Alzheimer's disease.
METHODS METHODS
The proposed project is a proof of concept study to test whether levetiracetam can help cognitive function in people with dementia. We plan to recruit thirty patients with mild to moderate Alzheimer's disease with no history of previous seizures or other significant co-morbidity. Participants will be allocated to a double-blind placebo-controlled crossover trial that tests levetiracetam against placebo. Standardised scales to assess cognition and a computer-based touchscreen test that we have developed to better detect subtle improvements in hippocampal function will be used to measure changes in memory. All participants will have an electroencephalogram (EEG) at baseline. The primary outcome measure is a change in the computer-based touchscreen cognitive task while secondary outcomes include the effect of levetiracetam on mood, quality of life and modelling of the EEG, including time series measures and feature-based analysis to see whether the effect of levetiracetam can be predicted. The effect of levetiracetam and placebo will be compared within a given patient using the paired t-test and the analysis of covariance adjusting for baseline values.
DISCUSSION CONCLUSIONS
This is the first study to evaluate if an anti-seizure medication can offer meaningful benefit to patients with Alzheimer's disease. If this study demonstrates at least stabilisation of memory function and/or good tolerability, the next step will be to rapidly progress to a larger study to establish whether levetiracetam may be a useful and cost-effective treatment for patients with Alzheimer's disease.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov NCT03489044 . Registered on April 5, 2018.

Identifiants

pubmed: 34332638
doi: 10.1186/s13063-021-05404-4
pii: 10.1186/s13063-021-05404-4
pmc: PMC8325256
doi:

Substances chimiques

Levetiracetam 44YRR34555

Banques de données

ClinicalTrials.gov
['NCT03489044']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

508

Subventions

Organisme : Medical Research Foundation
ID : Confidence in Concept - letter attached
Organisme : UCB Pharma
ID : Investigator initiated study - letter attached

Informations de copyright

© 2021. The Author(s).

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Auteurs

Arjune Sen (A)

Oxford Epilepsy Research Group, NIHR Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK. arjune.sen@ndcn.ox.ac.uk.
Department of Neurology, John Radcliffe Hospital, Oxford, OX3 9DU, UK. arjune.sen@ndcn.ox.ac.uk.
Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford, OX3 9DU, UK. arjune.sen@ndcn.ox.ac.uk.

Mary Akinola (M)

Local Clinical Trials Network, John Radcliffe Hospital, Oxford, OX3 9DU, UK.

Xin You Tai (XY)

Oxford Epilepsy Research Group, NIHR Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK.
Department of Neurology, John Radcliffe Hospital, Oxford, OX3 9DU, UK.

Mkael Symmonds (M)

Oxford Epilepsy Research Group, NIHR Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK.
Department of Clinical Neurophysiology, John Radcliffe Hospital, Oxford, OX3 9DU, UK.

Gabriel Davis Jones (G)

Oxford Epilepsy Research Group, NIHR Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK.
Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford, OX3 9DU, UK.

Sergio Mura (S)

Clinical Trials Pharmacy, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 9DU, UK.

Joanne Galloway (J)

CPSU, Oxford Health Foundation Trust, Oxford, OX1 5RW, UK.

Angela Hallam (A)

St Mary's Pharmaceutical Unit, Cardiff University, Cardiff, 20 Fieldway, Cardiff, CF14 4HY, UK.

Jane Y C Chan (JYC)

Freeline Therapeutics, King's Court, London Road, Stevenage, SG1 2NG, UK.
Translational Medicine, UCB Pharma, 208 Bath Road, Slough, SL1 3WE, UK.

Ivan Koychev (I)

Department of Psychiatry, University of Oxford, Oxford, OX3 7JX, UK.

Chris Butler (C)

Faculty of Medicine, Department of Brain Sciences, Imperial College, Sir Alexander Fleming Building, South Kensington Campus, London, SW7 2BU, UK.

John Geddes (J)

Department of Psychiatry, University of Oxford, Warneford Hospital, Oxford, OX3 7JX, UK.

Rohan Van Der Putt (R)

Memory and Cognition Research Delivery Team, Warneford Hospital, Warneford Lane, Headington, Oxford, OX3 7JX, UK.

Sian Thompson (S)

Department of Neurology, John Radcliffe Hospital, Oxford, OX3 9DU, UK.

Sanjay G Manohar (SG)

Department of Neurology, John Radcliffe Hospital, Oxford, OX3 9DU, UK.
Nuffield Department of Clinical Neuroscience, University of Oxford, Oxford, OX3 9DU, UK.

Eleni Frangou (E)

MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, Faculty of Pop Health Sciences, University College London, London, UK.
Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Windmill Road, Oxford, OX3 7LD, UK.

Sharon Love (S)

MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, Faculty of Pop Health Sciences, University College London, London, UK.
Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Windmill Road, Oxford, OX3 7LD, UK.

Rupert McShane (R)

Department of Psychiatry, University of Oxford, Warneford Hospital, Oxford, OX3 7JX, UK.

Masud Husain (M)

Oxford Epilepsy Research Group, NIHR Biomedical Research Centre, John Radcliffe Hospital, Oxford, UK.
Cognitive Neurology Research Group, Nuffield Dept Clinical Neurosciences & Department of Experimental Psychology, University of Oxford, West Wing, John Radcliffe Hospital, Oxford, OX3 9DU, UK.

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