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The neurobiological correlates of anhedonic depression in Parkinson*s disease; associations between dopamine function and functional pathways

The neurobiological correlates of anhedonic depression in Parkinson*s disease; associations between dopamine function and functional pathways - AnHedonic dEpression&Alteration in Dopamine-neurocircuit in Parkinson:AHEAD

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON54140
Enrollment
75
Registered
2020-09-14
Start date
2022-03-02
Completion date
Unknown
Last updated
2024-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

depression Parkinson's disease

Interventions

None listed

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: For the present study, we will select patients from the PPP and PRIME cohorts and from clinical samples from neurologists embedded in Parkinsonnet and/or in the service area of the RadboudUMC. The PPP study is a pro-spective, longitudinal, single-center cohort study of the Radboudumc in the Netherlands which started in October 2017. Enrollment period will take 2 years, in which a total of 650 adult patients diagnosed with PD with

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: Exclusion criteria: • Contraindications for MRI, e.g., claustrophobia, presence of an active implant, pacemaker, insulin pump, neurostimulator, ossicle prosthesis, pregnancy, and/or other medical device or other non-removable metal part incompatible with MRI. • Contraindications for PET e.g., inability to lie flat or lie still for the duration of the scan, claustrophobia (occasionally). • Use of medication or drugs with evident DAT-binding like methylphenidate, buproprion, amphetamines, cocaine that cannot be discontinued according to the PET-protocol. Note that we allow use of anti-depressants with the exception of those antidepressants with a high DAT binding defined as a relatively low Ki of

Design outcomes

Primary

MeasureTime frame
Differences between (anhedonic and non-anhedonic) depressed PD patients and non-depressed PD patients in: (1) Baseline DAT-availability measured with PET; (2) Functional connectivity from seeds with aberrant DAT-availability compared to non-depressed PD.

Secondary

MeasureTime frame
Differences between (anhedonic and non-anhedonic) depressed PD patients and non-depressed PD patients in effort-reward weighting on an effort-reward-choice-task (ERCT), fMRI-based BOLD signal when performing the ERCT during the decisional phase, fMRI-based BOLD signal when performing a reinforcement learning task, neuromelanin, and subjective self-report measurements assessing depression, anhedonia, apathy and anxiety.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)