Brain Changes by Rivastigmine According to Butyrylcholinesterase Alleles

Sponsor
Seoul National University Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT02063269
Collaborator
Novartis Korea Ltd. (Industry)
70
1
1
40
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Study Details

Study Description

Brief Summary

Butyrylcholinesterase (BuChE) activity is increasing in Alzheimer Disease (AD) process (Lane et al., 2006). BuChE wild type has stronger butyrylcholine esterase activity than BuChE K variant allele and this strong activity can affect AD brain negatively by choline depletion. Rivastigmine has unique dual action - acetylcholine esterase inhibition and butyrylcholine esterase inhibition. Therefore, rivastigmine can lower serum butyrylcholine esterase activity and delay functional decrease of Fluorodeoxyglucose positron emission tomography (FDG PET) images in AD patients with BuChE wild type allele by strong BuChE inhibition.

It suggests that rivastigmine can affect brain function differently by BuChE genotype in AD. Therefore, we will try to find the different changes of serum butyrylcholine esterase activity by ELISA and functional and structural changes of brain between BuChE wild type and K-variant type by FDG PET and MRI pre and post images after 12 month use of rivastigmine.

  1. Primary objective:

  2. the mean changes of Standardized Uptake Values (SUVmean) in PET imaging

  3. the mean changes of serum BuChE activity between BuChE wild type and K-variant type.

  4. Secondary objectives:

  5. the mean changes of cortical thickness in brain MRI

  6. the cognitive changes in Alzheimer's Disease Assessment Scale-cognitive subscale (ADAS-cog)

  7. the cognitive changes in Mini-Mental State Exam (MMSE)

  8. the daily function changes by Alzheimer's Disease Cooperative Study - Activities of Daily Living (ADCS-ADL)

  9. the behavioural changes by Caregiver-Administered Neuropsychiatric Inventory (NPI)

  10. the disease severity changes by Clinical Dementia Rating Scale-Sum of Boxes (CDR-SB) between BuChE wild type and K-variant type.

Condition or Disease Intervention/Treatment Phase
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Differences of Functional Changes in Brain by Rivastigmine According to Butyrylcholinesterase Alleles in Alzheimer's Disease Patients(Rivastigmine, Imaging, and BuChE in AD: RIBA)
Study Start Date :
Feb 1, 2014
Anticipated Primary Completion Date :
Jun 1, 2017
Anticipated Study Completion Date :
Jun 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Rivastigmine

Rivastigmine

Drug: Rivastigmine
9-18mg/rivastigmine for 52 weeks
Other Names:
  • Exelon
  • Outcome Measures

    Primary Outcome Measures

    1. the mean changes of Standardized Uptake Values (SUVmean) in PET imaging [screening and 52weeks (2 times)]

      Unit: mg/100g/min

    2. the mean changes of serum BuChE activity between BuChE wild type and K-variant type [screening and 52weeks (2 times)]

      unit of umil ACSCh/h/mg

    Secondary Outcome Measures

    1. the mean changes of cortical thickness in brain MRI [screening and 52weeks (2 times)]

      unit of mm

    2. the cognitive changes in Alzheimer's Disease Assessment Scale-cognitive subscale (ADAS-cog) [screening, 26, and 52 weeks (3 times)]

      unit in points

    3. the cognitive changes in Mini-Mental State Exam (MMSE) [screening, 26, and 52 weeks (3 times)]

      unit in points

    4. the daily function changes by Alzheimer's Disease Cooperative Study - Activities of Daily Living (ADCS-ADL) [screening, 26, and 52 weeks (3 times)]

      unit in points

    5. the behavioural changes by Caregiver-Administered Neuropsychiatric Inventory (NPI) [screening, 26, and 52 weeks (3 times)]

      unit in points

    6. the disease severity changes by Clinical Dementia Rating Scale-Sum of Boxes (CDR-SB) between BuChE wild type and K-variant type [screening, 26, and 52 weeks (3 times)]

      unit in points

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    55 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Clinical diagnosis of Alzheimer's Disease (NINCD-ADRDA and MMSE between 10 ~26)

    • Who didn't take Cholinesterase Inhibitor on liver within 3 months

    Exclusion Criteria:
    • diagnosed with diseases other than AD that affect brain atrophy according to Brain MRI

    • Diagnosed with diseases other than AD which affect cognitive functions (i.g. Schizophrenia, Major Depression, Mental Retardation, encephalopathy, etc.)

    • Didn't suspect of drug or alcohol addictions within last decade

    • Unable to participate the study due to poor sight and hearing

    • Who aren't suitable to participate according to the researchers' judgement

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Seoul Metropolitan Government Seoul National University Boramae Medical Center Seoul Korea, Republic of 156-707

    Sponsors and Collaborators

    • Seoul National University Hospital
    • Novartis Korea Ltd.

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Jun Young Lee, MD, Seoul National University Hospital
    ClinicalTrials.gov Identifier:
    NCT02063269
    Other Study ID Numbers:
    • CENA713DKR15T
    First Posted:
    Feb 14, 2014
    Last Update Posted:
    May 14, 2015
    Last Verified:
    May 1, 2015
    Keywords provided by Jun Young Lee, MD, Seoul National University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 14, 2015