As a postdoc in Rick Helmich's research group, you will use cutting-edge neuroimaging and neuromodulation techniques to investigate how the clinical phenotype of Parkinson's disease (PD) is shaped by longitudinal changes in compensatory brain mechanisms. This position aims to develop new biomarkers of brain compensation based on resting-state functional MRI. On this topic, we currently offer two postdoctoral researcher positions. This vacancy is for position 1. Position 2 aims to alleviate PD symptoms by enhancing brain compensation using modern non-invasive neuromodulation technology (low-intensity transcranial ultrasound sonification [TUS]). You are welcome to apply for both positions. In that case, it is sufficient to apply for 1 vacancy and clearly indicate in your letter that you are applying for both vacancies.
Background PD is a common, debilitating neurodegenerative condition characterized by motor and non-motor symptoms that worsen over time. The pathological hallmark of PD, progressive cell loss in the nigro-striatal dopaminergic system, cannot fully account for this worsening, suggesting that the clinical course of PD must be determined by additional brain mechanisms. In support of this, we recently demonstrated that the clinical phenotype of PD depends on the integrity of compensatory mechanisms located in parietal and premotor areas of the cerebral cortex.
This raises exciting questions about how cortical compensation changes over time, how these changes influence the progression of symptoms, and whether they can be targeted to manipulate the clinical course of PD. The aim of this project is to better understand the role that compensatory mechanisms play in shaping the clinical progression of PD. In pursuit of this aim, we offer two postdoctoral researcher positions that focus on different aspects of compensation: quantification and manipulation.
Position This position is funded by the EU Joint Programme - Neurodegenerative Disease Research and focuses on improving the quantification of compensation in clinically feasible environments. To achieve this, you will translate previously developed indices of brain compensation, acquired using task-based functional MRI, into the domain of resting-state functional MRI, where they can validated against measurements of compensation derived from MEG and PET data in independent cohorts.
In Nijmegen, you will be embedded in the research group of Dr. Rick Helmich at the Donders Institute, Centre for Cognitive Neuroimaging. In addition, you will take part in a collaboration between 4 countries (Netherlands, Germany, Sweden, Czech Republic). Your project will rely on an existing, unique longitudinal PD cohort (Personalized Parkinson Project, PPP) that is being followed in Nijmegen since 2018.
The PPP is a single-center longitudinal observational study in 520 early PD patients (0-5 years disease duration, 2-year observation period, yearly clinical evaluations). All patients undergo clinical assessments at Radboudumc in Nijmegen and all of them are scanned twice (baseline and after 2 years) with the same 3T MRI scanner at the Donders Institute.
Tasks - Use dynamic causal modelling (DCM) to derive neurophysiologically plausible indices of cortical compensation from task-based functional MRI.
- Adapt the DCM approach to resting-state functional MRI.
- Implement the resting-state based DCM approach in independent cohorts within the consortium and validate it against MEG and PET markers of compensation.
- Coordinate knowledge transfer within the international consortium.