The GBA Multimodal Study in Parkinson's Disease

Last updated: November 4, 2024
Sponsor: Pacific Parkinson's Research Centre
Overall Status: Active - Recruiting

Phase

N/A

Condition

Gaucher Disease

Treatment

neuroQWERTY

PET scan

Clinical Study ID

NCT04101968
16451
  • Ages 18-80
  • All Genders

Study Summary

This study plans to analyze the molecular and clinical mechanisms of the relationship between the GBA mutations and Parkinson's disease. This will be assessed through the use of advanced neuroimaging techniques called PET (positron emission tomography) to study the accumulation of the tau protein and the dysfunction of acetylcholine and dopamine in the brain of people with a mutation in the GBA gene, with and without Parkinson's disease. The ingestigators will also use a technology-based assessment to study the typing patterns as possible biomarkers of early motor dysfunctions.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • heterozygous for a pathogenic GBA mutation (e.g., p.L444P, p.N370S) or polymorphism;

  • age 18 to 80 years.

Exclusion

Exclusion Criteria:

  • co-occurrence of other neurological disorders;

  • implants that contraindicate the MRI scanning (e.g. cardiac pacemaker, ferromagneticimplants or devices);

  • severe claustrophobia;

  • intolerance to antiparkinsonian drug withdrawal (for GBA-PD subjects);

  • ongoing treatment with cholinergic drugs

Study Design

Total Participants: 25
Treatment Group(s): 2
Primary Treatment: neuroQWERTY
Phase:
Study Start date:
May 01, 2019
Estimated Completion Date:
December 30, 2025

Study Description

Study Rationale: People who have a mutation in the GBA gene have a higher risk of developing Parkinson's disease (PD) and, if they have PD, are more likely to have cognitive decline and dementia. Cognitive problems in people with PD is related to dysfunction of the brain chemical acetylcholine and likely to the accumulation of the tau protein in the brain. Another observation in previous studies is that analyzing the patterns of typing into a computer can help differentiate healthy people from people with PD.

Hypothesis: The investigators hypothesize that people with GBA-related PD will have higher acetylcholine dysfunction and tau accumulation compared with non-GBA patients, and that these changes may start in the asymptomatic phase (i.e., people with the mutation but without symptoms of PD). The investigators also believe that the investigators will be able to detect subjects with higher degree of dopamine loss just by analyzing the way they type into a computer.

Study Design: The investigators will recruit 25 subjects with a GBA mutation (10 subjects with PD and 15 asymptomatic carriers). All the participants will have a clinical evaluation and a typing session, and subsequently will undergo a brain MRI and three PET scans with a tau tracer, an acetylcholine tracer, and a dopaminergic tracer. A blood sample will also be taken for the analysis of GCase (the enzyme related to the GBA mutation).

Impact on Diagnosis/Treatment of Parkinson's Disease: The results will help understand the changes that take place in the brain of people with GBA-related Parkinson's disease, and hopefully will shed light also on the pathophysiology of non-GBA-related Parkinson's, as well as on the molecular correlates of cognitive decline, especially in its early stage. The typing data along with dopaminergic imaging will clarify the possible role of using typing patterns to identify subjects with early stage Parkinson's disease.

Next Steps for Development: The findings of this study may help identify biomarkers for cognitive decline in early Parkinson's disease, with a potential role in clinical trials. Also, if the hypothesis on the typing is confirmed, this approach may be studied in larger cohorts for early diagnosis of Parkinson's in other at-risk populations.

Connect with a study center

  • Pacific Parkinson's Research Centre | University of British Columbia

    Vancouver, British Columbia
    Canada

    Active - Recruiting

  • Oregon Health & Science University

    Portland, Oregon 97239
    United States

    Active - Recruiting

  • University of Washington

    Seattle, Washington 98108-1595
    United States

    Active - Recruiting

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