Elucidating the Role of Cholinergic Degeneration in Cognitive Fluctuations in Lewy Body Dementia
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About
The proposed study aims to address the critical gaps in understanding the mechanisms of CF (Cognitive Fluctuations) by leveraging recently emerged molecular biomarkers, advanced neuroimaging techniques to assess measures of cholinergic degeneration, and synchronous EEG and assessments of attention. One of the overarching innovations of study is combining all of these assessments into one integrated research plan
Full description
Aim 1 is a cross-sectional case control study in which cholinergic degeneration in 45 participants with DLB or PDD with CF will be compared to a group of 45 individuals with Lewy Body disease without CF and 30 healthy controls. The first 20 participants who are eligible for Aim 2 and consent will also participate in an 8-week pre-post interventional cohort study immediately following Aim 1 procedures. For Aim 3, Aim 1 participants will complete annual follow-up evaluations for 2 years to understand factors influencing the change in cognitive fluctuations over time.
Enrollment
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Volunteers
Inclusion criteria
Arm 1:
- Age range: 50 ≤ age < 90.
- Diagnosis of dementia with Lewy bodies (DLB), Parkinson disease dementia (PDD), Parkinson disease with Mild Cognitive Impairment (PD-MCI), Mild Cognitive Impairment with Lewy bodies (MCI-LB).
- DLB participants must fulfill criteria for clinically probable DLB based on the 2017 4th consensus report of the DLB consortium.
- PDD participants must meet criteria for clinically probable PD according to the MDS Clinical Diagnostic Criteria for Parkinson's Disease and must also meet criteria for probable PDD based on the 2007 Movement Disorders Society clinical diagnostic criteria.
- PD-MCI participants must meet criteria for clinically probable PD according to the MDS Clinical Diagnostic Criteria for Parkinson's Disease and meet criteria for Mild Cognitive Impairment on cognitive testing at screening.
- MCI-LB participants with must meet established research criteria.
- Capacity to provide informed consent or, if unable, availability of a legally authorized representative or guardian who can provide informed consent.
- Availability of informant (for participants meeting criteria for dementia).
- Ability and willingness to comply with the study-related procedures.
- Fluent in spoken and written English (due to cognitive testing)
Exclusion criteria
Arm 1
- History of cognitive disorder or psychiatric disorder other than that related to dementia with Lewy bodies or Parkinson disease dementia.
- History of deep brain stimulation or any neurosurgical procedure.
- History of structural brain disease or known significant cerebrovascular disease.
- History of seizures or epilepsy and/or use of sodium channel blockers, i.e. carbamazepine, oxcarbazepine, phenytoin, topiramate, lamotrigine, felbamate, zonisamide, rufinamide, lacosamide, eslicarbazepine, and valproate.
- Greater than two alcoholic drinks per day for men and one per day for women.
- Regular use of benzodiazepines or barbiturates. (If benzodiazepines are taken as needed only, these medications cannot be taken within 5 half-lives of screening visit or between screening visit and EEG.)
- Severe dementia (based on PI assessment of subject dependence level for instrumental activities of daily living)
- Any contraindication to brain MRI.
- Any medical condition that would interfere with ability to complete all study procedures.
- Participants must not be pregnant, planning to become pregnant, or father a child for the duration of the study
Inclusion Criteria:
Arm 2 (Cholinesterase inhibitor cohort) inclusion criteria:
- Completed Aim 1.
- Clinical diagnosis of LBD (DLB or PDD) with CF.
- Not taking a cholinesterase inhibitor and has not taken a cholinesterase inhibitor in the previous 90 days.
- Ability and willingness to comply with the ChEI Cohort procedures (including galantamine administration), or a caregiver willing and able to ensure compliance.
Exclusion Criteria:
Arm 2 (Cholinesterase inhibitor cohort) exclusion criteria:
- Severe hepatic impairment.
- Renal failure.
- Significant bradycardia (<50 bpm) at screening or history of AV block.
- Any contraindication to galantamine administration based on PI discretion.
Inclusion criteria:
Arm 3 (Healthy Controls)
- Age range: 50 ≤ age < 90.
- Healthy controls should not have any known neurologic conditions that could interfere with study procedures or results.
- Capacity to provide informed consent or, if unable, availability of a legally authorized representative or guardian who can provide informed consent.
- Availability of informant (for participants meeting criteria for dementia).
- Ability and willingness to comply with the study-related procedures.
- Fluent in spoken and written English (due to cognitive testing).
Exclusion Criteria:
Arm 3 (Healthy Controls)
- No History of cognitive disorder or psychiatric disorder other than that related to dementia with Lewy bodies or Parkinson disease dementia.
- No History of deep brain stimulation or any neurosurgical procedure.
- No History of structural brain disease or known significant cerebrovascular disease.
- No History of seizures or epilepsy and/or use of sodium channel blockers, i.e. carbamazepine, oxcarbazepine, phenytoin, topiramate, lamotrigine, felbamate, zonisamide, rufinamide, lacosamide, eslicarbazepine, and valproate.
- Any medical condition that would interfere with ability to complete all study procedures.
- Participants must not be pregnant, planning to become pregnant, or father a child for the duration of the study
Trial design
Primary purpose
Allocation
Interventional model
Masking
120 participants in 3 patient groups
Trial contacts and locations
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Central trial contact
Kara McHaney
Data sourced from clinicaltrials.gov
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