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Neuroimaging biomarkers for clinical trials in atypical parkinsonian disorders: Proposal for a Neuroimaging Biomarker Utility System

Nico Bohnen; Alessandro Tessitore; Stephane Lehericy; Axel Rominger; Oury Monchi; José Ángel Pineda-Pardo; Angelo Antonini; Alexander Drzezga; Matej Ondrus; Stephane Thobois; María Rodríguez-Oroz; Antonio P. Strafella; Gregor Wenning; Simon Lewis; Makoto Higuchi; Klaus Seppi; Peter Nestor; James B. Rowe; for the MDS Neuroimaging Study Group and the JPND Working Group ASAP-SynTau; María Cecilia Peralta; Thilo van Eimeren; Daniela Berg; Irena Rektorová; Hartwig R. Siebner; Roberto Ceravolo; Paola Piccini; A. Jon Stoessl; Günter U. Höglinger; Valtteri Kaasinen; Nicola Pavese

Neuroimaging biomarkers for clinical trials in atypical parkinsonian disorders: Proposal for a Neuroimaging Biomarker Utility System

Nico Bohnen
Alessandro Tessitore
Stephane Lehericy
Axel Rominger
Oury Monchi
José Ángel Pineda-Pardo
Angelo Antonini
Alexander Drzezga
Matej Ondrus
Stephane Thobois
María Rodríguez-Oroz
Antonio P. Strafella
Gregor Wenning
Simon Lewis
Makoto Higuchi
Klaus Seppi
Peter Nestor
James B. Rowe; for the MDS Neuroimaging Study Group and the JPND Working Group ASAP-SynTau
María Cecilia Peralta
Thilo van Eimeren
Daniela Berg
Irena Rektorová
Hartwig R. Siebner
Roberto Ceravolo
Paola Piccini
A. Jon Stoessl
Günter U. Höglinger
Valtteri Kaasinen
Nicola Pavese
Katso/Avaa
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Lataukset: 

Elsevier Inc
doi:10.1016/j.dadm.2019.01.011
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042821870
Tiivistelmä


Introduction

Therapeutic strategies targeting protein aggregations are ready for clinical trials in atypical parkinsonian disorders. Therefore, there is an urgent need for neuroimaging biomarkers to help with the early detection of neurodegenerative processes, the early differentiation of the underlying pathology, and the objective assessment of disease progression. However, there currently is not yet a consensus in the field on how to describe utility of biomarkers for clinical trials in atypical parkinsonian disorders.


Methods

To promote standardized use of neuroimaging biomarkers for clinical trials, we aimed to develop a conceptual framework to characterize in more detail the kind of neuroimaging biomarkers needed in atypical parkinsonian disorders, identify the current challenges in ascribing utility of these biomarkers, and propose criteria for a system that may guide future studies.


Results

As a consensus outcome, we describe the main challenges in ascribing utility of neuroimaging biomarkers in atypical parkinsonian disorders, and we propose a conceptual framework that includes a graded system for the description of utility of a specific neuroimaging measure. We included separate categories for the ability to accurately identify an intention-to-treat patient population early in the disease (Early), to accurately detect a specific underlying pathology (Specific), and the ability to monitor disease progression (Progression).


Discussion

We suggest that the advancement of standardized neuroimaging in the field of atypical parkinsonian disorders will be furthered by a well-defined reference frame for the utility of biomarkers. The proposed utility system allows a detailed and graded description of the respective strengths of neuroimaging biomarkers in the currently most relevant areas of application in clinical trials.

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