TY - JOUR
T1 - The Luxembourg Parkinson's Study
T2 - A comprehensive approach for stratification and early diagnosis
AU - Hipp, Geraldine
AU - Vaillant, Michel
AU - Diederich, Nico J.
AU - Roomp, Kirsten
AU - Satagopam, Venkata P.
AU - Banda, Peter
AU - Sandt, Estelle
AU - Mommaerts, Kathleen
AU - Schmitz, Sabine K.
AU - Longhino, Laura
AU - Schweicher, Alexandra
AU - Hanff, Anne Marie
AU - Nicolai, Béatrice
AU - Kolber, Pierre
AU - Reiter, Dorothea
AU - Pavelka, Lukas
AU - Binck, Sylvia
AU - Pauly, Claire
AU - Geffers, Lars
AU - Betsou, Fay
AU - Gantenbein, Manon
AU - Klucken, Jochen
AU - Gasser, Thomas
AU - Hu, Michele T.
AU - Balling, Rudi
AU - Krüger, Rejko
N1 - Publisher Copyright:
Copyright © 2018 Hipp, Vaillant, Diederich, Roomp, Satagopam, Banda, Sandt, Mommaerts, Schmitz, Longhino, Schweicher, Han, Nicolai, Kolber, Reiter, Pavelka, Binck, Pauly, Geers, Betsou, Gantenbein, Klucken, Gasser, Hu, Balling and Krüger.
PY - 2018
Y1 - 2018
N2 - 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.
AB - 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.
KW - Cohort
KW - Deep phenotyping
KW - Longitudinal
KW - Parkinsonism
KW - Stratification
UR - http://www.scopus.com/inward/record.url?scp=85058847422&partnerID=8YFLogxK
U2 - 10.3389/fnagi.2018.00326
DO - 10.3389/fnagi.2018.00326
M3 - Article
AN - SCOPUS:85058847422
SN - 1663-4365
VL - 10
JO - Frontiers in Aging Neuroscience
JF - Frontiers in Aging Neuroscience
M1 - 326
ER -