Frontiers in Aging Neuroscience (Oct 2018)

The Luxembourg Parkinson’s Study: A Comprehensive Approach for Stratification and Early Diagnosis

  • Geraldine Hipp,
  • Geraldine Hipp,
  • Michel Vaillant,
  • Nico J. Diederich,
  • Kirsten Roomp,
  • Venkata P. Satagopam,
  • Peter Banda,
  • Estelle Sandt,
  • Kathleen Mommaerts,
  • Kathleen Mommaerts,
  • Sabine K. Schmitz,
  • Laura Longhino,
  • Alexandra Schweicher,
  • Anne-Marie Hanff,
  • Béatrice Nicolai,
  • Pierre Kolber,
  • Pierre Kolber,
  • Dorothea Reiter,
  • Dorothea Reiter,
  • Lukas Pavelka,
  • Lukas Pavelka,
  • Sylvia Binck,
  • Sylvia Binck,
  • Claire Pauly,
  • Claire Pauly,
  • Lars Geffers,
  • Fay Betsou,
  • Manon Gantenbein,
  • Jochen Klucken,
  • Thomas Gasser,
  • Michele T. Hu,
  • Rudi Balling,
  • Rejko Krüger,
  • Rejko Krüger

DOI
https://doi.org/10.3389/fnagi.2018.00326
Journal volume & issue
Vol. 10

Abstract

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While genetic advances have successfully defined part of the complexity in Parkinson’s disease (PD), the clinical characterization of phenotypes remains challenging. Therapeutic trials and cohort studies typically include patients with earlier disease stages and exclude comorbidities, thus ignoring a substantial part of the real-world PD population. To account for these limitations, we implemented the Luxembourg PD study as a comprehensive clinical, molecular and device-based approach including patients with typical PD and atypical parkinsonism, irrespective of their disease stage, age, comorbidities, or linguistic background. To provide a large, longitudinally followed, and deeply phenotyped set of patients and controls for clinical and fundamental research on PD, we implemented an open-source digital platform that can be harmonized with international PD cohort studies. Our interests also reflect Luxembourg-specific areas of PD research, including vision, gait, and cognition. This effort is flanked by comprehensive biosampling efforts assuring high quality and sustained availability of body liquids and tissue biopsies. We provide evidence for the feasibility of such a cohort program with deep phenotyping and high quality biosampling on parkinsonism in an environment with structural specificities and alert the international research community to our willingness to collaborate with other centers. The combination of advanced clinical phenotyping approaches including device-based assessment will create a comprehensive assessment of the disease and its variants, its interaction with comorbidities and its progression. We envision the Luxembourg Parkinson’s study as an important research platform for defining early diagnosis and progression markers that translate into stratified treatment approaches.

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