MADE: Melatonin in Alzheimer's Disease: Effect on Disease Progression and Epileptiform Activity.

Sponsor
Universitair Ziekenhuis Brussel (Other)
Overall Status
Recruiting
CT.gov ID
NCT04522960
Collaborator
(none)
60
1
2
32.3
1.9

Study Details

Study Description

Brief Summary

This is a long-term, prospective, observational study to investigate and compare the levels and rhythm of melatonin in patients with AD dementia, mild cognitive impairment due to AD and healthy volunteers. The investigators would like to validate the use of salivary and urine melatonin measurements as an alternative for blood/CSF melatonin. Furthermore, the investigators would like to assess the effects of melatonin levels on cognition by correlating the levels and changes on cognitive tasks over a two year time frame. The investigators will also investigate whether these effects could be due to its anticonvulsive properties.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: MEG+hdEEG+MRI
N/A

Detailed Description

Melatonin production gets disrupted in AD, as shown in post-mortem pineal glands and CSF of AD patients. CSF melatonin levels are known to significantly drop in patients with Alzheimer's dementia. It is known that CSF melatonin levels are much higher than blood melatonin levels, due to melatonin secretion from the pineal recess directly into the third ventricle. It has never been investigated whether blood melatonin accurately correlates with CSF melatonin in AD, nor whether saliva or urine melatonin levels accurately reflect blood/CSF melatonin in the AD continuum. The investigators want to validate the use of blood, saliva and urine melatonin levels as alternative for CSF melatonin in the AD continuum to pave the way for further use of less invasive collection techniques (blood, saliva, urine instead of CSF) and to possibly study circadian rhythm in a less disrupting, in home environment (saliva, urine).

Furhtermore, melatonin exerts several potential anti-AD properties, including anti-inflammatory, anti-oxidant, tilting APP processing towards the non-amyloidogenic pathway, exerting positive effects on sleep and so on. In vivo studies furthermore point to anticonvulsive and antiepileptic effects of melatonin in a whole range of rodent models. Some evidence exists for a role of melatonin in prevention of epileptic seizures in humans.

The investigators want to investigate influence of melatonin on changes in cognition in a longitudinal way, and investigate influence on (sub)clinical epileptiform activity.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Melatonin in Alzheimer's Disease: Effect on Disease Progression and Epileptiform Activity.
Actual Study Start Date :
Oct 20, 2020
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Jul 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Patients with dementia or mild cognitive impairment due to AD

Dementia or MCI due to AD according to NIA-AA research criteria.

Diagnostic Test: MEG+hdEEG+MRI
We will perform several tests: Neuropsychological testing to evaluate evolution of cognition during our study. Lumbar puncture, blood sampling, saliva and urine collection to assess melatonin levels at several timepoints within these biological fluids. MEG+hdEEG and MRI (to project MEG information) ; LTM-EEG to detect epileptiform activity in patients and healthy controls
Other Names:
  • Lumbar puncture
  • Long-term EEG monitoring
  • Blood sampling
  • Saliva collection
  • Urine collection
  • Neuropsychological examination
  • Active Comparator: Healthy volunteers

    Age-and-gender matched healthy controls.

    Diagnostic Test: MEG+hdEEG+MRI
    We will perform several tests: Neuropsychological testing to evaluate evolution of cognition during our study. Lumbar puncture, blood sampling, saliva and urine collection to assess melatonin levels at several timepoints within these biological fluids. MEG+hdEEG and MRI (to project MEG information) ; LTM-EEG to detect epileptiform activity in patients and healthy controls
    Other Names:
  • Lumbar puncture
  • Long-term EEG monitoring
  • Blood sampling
  • Saliva collection
  • Urine collection
  • Neuropsychological examination
  • Outcome Measures

    Primary Outcome Measures

    1. CSF and blood melatonin levels in patients with AD dementia, MCI due to AD and healthy volunteers [24 hours]

      Comparison of CSF and blood melatonin levels between patients with MCI and dementia due to AD and healthy volunteers.

    2. Blood, saliva and urine melatonin correlations [24 hours]

      Correlation between blood melatonin and urinary and salivary melatonin in the AD continuum

    3. Melatonin influence on cognition [2 years]

      Correlations between melatonin levels and cognitive performance over a 2 year time frame. This will be assessed by use of neuropsychological testing including MMSE, MoCA, RBANS, VAT, ...

    4. Melatonin influence on epileptiform activity [8 weeks]

      Correlations between melatonin levels and (subclinical) epileptiform activity. Over a time frame of 8 weeks patients will undergo neuropsychological testing (with MMSE, MoCA, RBANS, VAT...), LTM-EEG monitoring (during 24 hours), MEG + hdEEG.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. Dementia due to AD, according to National Institute on Aging-Alzheimer's Association (NIA-AA) criteria

    2. MCI due to AD, according to NIA-AA criteria

    3. Healthy controls: Age- and gender matched healthy controls

    Exclusion Criteria:

    Patients (AD dementia, MCI)

    • Age < 18 years old

    • Pregnancy

    • Expected death due to illness within 2 years

    • Pacemaker or other ferrromagnetic material that is not MRI compatible

    • Other neurodegenerative or cerebrovascular disease

    • Pattern compatible with NPH (clinically, imaging)

    • Epilepsy

    • Multiple sclerosis or other demyelinating disease

    • Depression, psychosis or other mental disease

    • Use of anti-epileptic drugs

    • Alcohol or substance abuse

    • Korsakoff syndrome

    • Symptomatic liver disease

    • Uncontrolled thyroid disorders

    • Untreated HIV or syphilis

    • Clinically significant vitamin B12 deficiency

    • Severe systemic medical illness (eg end-stage cardiac disease, …)

    • Use of melatonin, agomelatine, or other sleep medications

    • Night worker

    • REM sleep behavior disorder, OSAS

    Healthy controls

    • Age < 18 years old

    • Pregnancy

    • Pacemaker or other ferromagnetic material that is not MRI compatible

    • Mild cognitive impairment or dementia of any cause

    • Epilepsy

    • Multiple sclerosis or other demyelinating disease

    • Depression, psychosis or other mental disease

    • Use of anti-epileptic drugs

    • Alcohol or substance abuse

    • Symptomatic liver disease

    • Uncontrolled thyroid disorders

    • Untreated HIV or syphilis

    • Clinically significant vitamin B12 deficiency

    • Severe systemic medical illness (eg end-stage cardiac disease, …)

    • Use of melatonin, agomelatine, or other sleep medications

    • Night worker

    • REM sleep behavior disorder, OSAS

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Universitair Ziekenhuis Brussel Brussels Jette Belgium 1090

    Sponsors and Collaborators

    • Universitair Ziekenhuis Brussel

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Universitair Ziekenhuis Brussel
    ClinicalTrials.gov Identifier:
    NCT04522960
    Other Study ID Numbers:
    • UZB-NEU-002
    First Posted:
    Aug 21, 2020
    Last Update Posted:
    May 18, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 18, 2022