Imaging a Cholinergic Biomarker of Cognition in Parkinson's Disease

NCT05034263 | Terminated

• 1 other identifier: 2020-00669
• Study Type: observational
• Target: 6
• Locations: 1 country
• Sites: 1

Brief Summary

This is an imaging study designed to illuminate the function of the cholinergic system and its association with cognitive skills in people with Parkinson's disease. The hypothesis of this study is that there will be an association between cholinergic terminal density, sex hormones, and cognitive functioning. Participants will receive a PET and MRI scan along with a battery of neurocognitive tests at baseline and again at 18 months follow-up. Hormone levels will be measured at baseline.

Conditions

Parkinson's Disease

Keywords

Acetylcholine; PET; MRI

Outcome Measures

Primary Outcomes (29)

• Cholinergic terminal density at baseline

  Measured by PET scan 18F\[VAT\] distribution volume

  Baseline

• Cholinergic terminal density change between baseline and 18-months follow-up

  Measured by the difference in PET scan 18F\[VAT\] distribution volume at baseline and 18-months follow-up

  Baseline and 18 months follow-up

• Overall cognitive functioning at baseline

  As measured by the Montreal Cognitive Assessment (MoCA). The MoCA measures eight domains commonly affected by mild cognitive impairment. The one-page 30-point test includes assessments of short-term and delayed memory recall, visuospatial abilities, language, orientation to time and space, and executive functions including attention, concentration, and working memory. The MoCA has been shown to be sensitive to change over time. Scores on the MocA range from 0-30 with higher scores indicating better cognitive functioning.

  Baseline

• Change in overall cognitive functioning

  As measured by the difference between the Montreal Cognitive Assessment (MoCA) score at baseline and at 18-months follow-up.The MoCA measures eight domains commonly affected by mild cognitive impairment. The one-page 30-point test includes assessments of short-term and delayed memory recall, visuospatial abilities, language, orientation to time and space, and executive functions including attention, concentration, and working memory. The MoCA has been shown to be sensitive to change over time. Scores on the MocA range from 0-30 with higher scores indicating better cognitive functioning.

  Baseline and 18 Months

• Attention/working memory at baseline as measured by the Trail Making A Test

  The Trail Making Test is a quickly and easily administered test which assesses cognitive abilities such as visual-conceptual and visual-motor tracking, sustained attention, and task alternation abilities. Administration time for the Trail Making Test A is 5 minutes.

  Baseline

• Attention/working memory change from baseline to 18-months follow-up as measured by the Trail Making A Test

  The Trail Making Test is a quickly and easily administered test which assesses cognitive abilities such as visual-conceptual and visual-motor tracking, sustained attention, and task alternation abilities. Administration time for the Trail Making Test A is 5 minutes.

  18 months

• Attention/working memory at baseline as measured by the Symbol Digit Modalities Test (SDMT)

  Symbol Digit Modalities Test (SDMT) takes five minutes to complete and has demonstrated sensitivity in detecting changes in cognitive functioning over time.

  Baseline

• Attention/working memory change from baseline to 18-months follow-up as measured by the Symbol Digit Modalities Test

  Symbol Digit Modalities Test (SDMT) takes five minutes to complete and has demonstrated sensitivity in detecting changes in cognitive functioning over time.

  Baseline and 18- months follow-up

• Executive function at baseline as measured by the Clock Drawing Test

  The Clock Drawing Test is a quick screening test for cognitive dysfunction secondary to a range of neurological disorders and takes less than 5 minutes to administer.

  Baseline

• Executive function change from baseline to 18-months follow-up as measured by the Clock Drawing Test

  The Clock Drawing Test is a quick screening test for cognitive dysfunction secondary to a range of neurological disorders and takes less than 5 minutes to administer.

  Baseline and 18-month follow-up

• Executive function at baseline as measured by the Trail Making Test B

  The Trail Making Test is a quickly and easily administered test which assesses cognitive abilities such as visual-conceptual and visual-motor tracking, sustained attention, and task alternation abilities. Administration time for the Trail Making Test B is 10 minutes.

  Baseline

• Executive function change from baseline to 18-months follow-up as measured by the Trail Making Test B

  The Trail Making Test is a quickly and easily administered test which assesses cognitive abilities such as visual-conceptual and visual-motor tracking, sustained attention, and task alternation abilities. Administration time for the Trail Making Test B is 10 minutes.

  Baseline and 18-month follow-up

• Language at baseline as measured by the Animal Naming Test

  The Animal Naming Test is a semantic fluency test that takes one minute to administer.

  Baseline

• Language change from baseline to 18-month follow-up as measured by the Animal Naming Test

  The Animal Naming Test is a semantic fluency test that takes one minute to administer.

  Baseline and 18-months follow-up

• Language at baseline as measured by the Boston Naming Test

  The Boston Naming Test measures confrontational word retrieval and takes about 15 minutes to administer.

  Baseline

• Language change from baseline to 18-months follow-up as measured by the Boston Naming Test

  The Boston Naming Test measures confrontational word retrieval and takes about 15 minutes to administer.

  Baseline and 18-months follow-up

• Language change between baseline and 18-month follow-up as measured by the Boston Naming Test

  The Boston Naming Test measures confrontational word retrieval and takes about 15 minutes to administer.

  Baseline

• Memory at baseline as measured by the Free and Cued Selective Reminding Test

  The Free and Cued Selective Reminding Test is an episodic memory test which assesses immediate and delayed free and cued-facilitated recall.

  Baseline

• Memory change from baseline to 18-months follow-up as measured by the Free and Cued Selective Reminding Test

  The Free and Cued Selective Reminding Test is an episodic memory test which assesses immediate and delayed free and cued-facilitated recall.

  Baseline and 18-months follow-up

• Memory at baseline as measured by the Brief Visuospatial Memory Test-Revised Selective Reminding Test

  The Brief Visuospatial Memory Test-Revised is a brief measure of visuospatial memory that takes approximately 45 minutes to administer.

  Baseline

• Memory change from baseline to 18-months follow-up as measured by the Brief Visuospatial Memory Test-Revised

  The Brief Visuospatial Memory Test-Revised is a brief measure of visuospatial memory that takes approximately 45 minutes to administer.

  Baseline and 18-months follow-up

• Memory change between baseline and 18-month follow-up

  As measured by the change in Free and Cued Selective Reminding Test and the Brief Visuospatial Memory Test-Revised scores at baseline and at 18-months follow-up.

  Baseline and 18-month follow-up

• Visuospatial at baseline as measured by the Judgement of Line Orientation Test

  Judgement of Line Orientation measures visuospatial perception and takes less than 15 minutes to administer.

  Baseline

• Visuospatial change from baseline to 18-months follow-up as measured by the Judgement of Line Orientation Test

  Judgement of Line Orientation measures visuospatial perception and takes less than 15 minutes to administer.

  Baseline and 18-months follow-up

• Visuospatial at baseline as measured by the Intersecting Pentagons Test

  Intersecting Pentagons is a measure of visuospatial sense that takes less than 5 minutes to administer.

  Baseline

• Visuospatial change from baseline to 18-months follow-up as measured by the Intersecting Pentagons Test

  Intersecting Pentagons is a measure of visuospatial perception that takes less than 5 minutes to administer.

  Baseline and 18-months follow-up

• Estrogen levels in blood at baseline

  Estrogen levels (picograms of estradiol per milliliter of serum) will be measured via blood draw performed at baseline

  Baseline

• Progesterone levels in blood as baseline

  Progesterone levels (nanograms of progesterone per milliliter of serum) will be measured via blood draw at baseline

  Baseline

• Testosterone levels in blood at baseline

  Levels of free testosterone (picograms testosterone per milliliter serum) and total testosterone (nanograms testosterone/deciliter serum) will be measured via blood draw performed at the baseline visit.

  Baseline

Secondary Outcomes (6)

• Cholinergic terminal binding potential at baseline

  Baseline

• Cholinergic terminal binding potential change between baseline and 18-months follow-up

  Baseline and 18-month follow-up

• MRI Fractional anisotropy (FA) Values at baseline

  Baseline

• Change in MRI Fractional anisotropy (FA) Values from baseline to 18-months follow-up

  Baseline and 18-months follow-up

• MRI Resting-state functional connectivity at baseline

  Baseline

Eligibility Criteria

• Age: 50 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

People with Parkinson's disease who have normal cognition or mild cognitive impairment

You may qualify if:

• Age 50-80
• Diagnosis of Parkinson's disease
• Ability to provide informed consent
• Ability to speak English
• Normal cognition or mild cognitive impairment
• Willingness to go off parkinsonian medication for 12 hours prior to two of the study visits

You may not qualify if:

• Contraindication for MRI
• Abnormal clinical brain MRI, specifically with evidence of large-vessel stroke or mass lesion
• History of stereotactic or ablative brain surgery
• Pregnancy
• Recent participation in other research studies involving radiation such that the annual research radiation dose would exceed FDA Limit if participating in this study
• Prior brain injury (eg., TBI)
• Baseline cognitive impairment due to genetic or developmental disorder
• Active illicit drug use or alcohol abuse
• Incapable of staying still for a 2-hour PET or MRI study
• Use of CNS-penetrating medications affecting the cholinergic system, including cholinesterase inhibitors and anticholinergics, up to 60 days prior to study participation

Sponsors & Collaborators

• Stony Brook University: lead
• Parkinson's Foundation: collaborator

Study Sites (1)

Stony Brook Medical Center

Stony Brook, New York, 11794, United States

Location

MeSH Terms

Conditions

Parkinson Disease

Condition Hierarchy (Ancestors)

Parkinsonian Disorders; Basal Ganglia Diseases; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Movement Disorders; Synucleinopathies; Neurodegenerative Diseases

Study Officials

• Chuan Huang, PhD

  Stony Brook Medical Center

  PRINCIPAL INVESTIGATOR

• Carine Maurer, PhD

  Stony Brook Medical Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Assistant Professor of Radiology

Study Record Dates

• First Submitted: August 17, 2021
• First Posted: September 5, 2021
• Study Start: May 27, 2021
• Primary Completion: May 27, 2024
• Study Completion: May 27, 2024
• Last Updated: April 6, 2025

Record last verified: 2025-04

Locations

US (1)