Evidence map›Paper›PMID 39147806›Full record

ArticleNPJ Parkinson's disease2024

Risk willingness in multiple system atrophy and Parkinson's disease understanding patient preferences.

Alexander Maximilian Bernhardt, Marc Oeller, Isabel Friedrich, Emre Kocakavuk, Eliana Nachman, Kevin Peikert, Malte Roderigo, Andreas Rossmann, Tabea Schröter, Lea Olivia Wilhelm and 21 more

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors.

Alexander Maximilian BernhardtDepartment of Neurology, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID http://orcid.org/0000-0002-2572-5062
Marc OellerDepartment for Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany. oeller@biochem.mpg.de.ORCID http://orcid.org/0000-0003-0597-5950
Isabel FriedrichDepartment of Neurology, University of Leipzig Medical Center, Leipzig, Germany.
Emre KocakavukDepartment of Hematology and Stem Cell Transplantation, West German Cancer Center, University Hospital Essen, Essen, Germany.
Eliana NachmanVIB Center for Brain & Disease Research, Leuven, Belgium.ORCID http://orcid.org/0000-0002-2069-6469
Kevin PeikertTranslational Neurodegeneration Section "Albrecht Kossel", Department of Neurology, University Medical Center Rostock, University of Rostock, Rostock, Germany.ORCID http://orcid.org/0000-0002-0845-2453
Malte RoderigoDepartment of Neurology with Institute of Translational Neurology, University of Muenster, Muenster, Germany.
Andreas RossmannDepartment of Cardiology, Augustinum Klinik München, München, Germany.
Tabea SchröterDepartment of Neurology, Jena University Hospital, Jena, Germany.
Lea Olivia WilhelmMedical School Berlin, Berlin, Germany.
Tino PrellDepartment of Neurology, Jena University Hospital, Jena, Germany.ORCID http://orcid.org/0000-0002-6423-3108
Christoph van RiesenDepartment of Neurology, University Medical Center Göttingen, Göttingen, Germany.
Johanna NiewelerDepartment of Neurology, University Medical Center Göttingen, Göttingen, Germany.
Sabrina KatzdoblerDepartment of Neurology, Ludwig-Maximilians-Universität München, Munich, Germany.
Markus WeilerDepartment of Neurology, Heidelberg University Hospital, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-8942-7662
Heike JacobiDepartment of Neurology, Heidelberg University Hospital, Heidelberg, Germany.
Tobias WarneckeDepartment of Neurology with Institute of Translational Neurology, University of Muenster, Muenster, Germany.
Inga ClausDepartment of Neurology with Institute of Translational Neurology, University of Muenster, Muenster, Germany.
Carla PalleisDepartment of Neurology, Ludwig-Maximilians-Universität München, Munich, Germany.
Stephan BreimannGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Björn FalkenburgerDepartment of Neurology, TU Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-2387-526X
Moritz BrandtDepartment of Neurology, TU Dresden, Dresden, Germany.
Andreas HermannTranslational Neurodegeneration Section "Albrecht Kossel", Department of Neurology, University Medical Center Rostock, University of Rostock, Rostock, Germany.
Jost-Julian RumpfDepartment of Neurology, University of Leipzig Medical Center, Leipzig, Germany.
Joseph ClaßenDepartment of Neurology, University of Leipzig Medical Center, Leipzig, Germany.ORCID http://orcid.org/0000-0001-7182-6967
Günter HöglingerDepartment of Neurology, Ludwig-Maximilians-Universität München, Munich, Germany.
Florin GandorMovement Disorders Clinic, Beelitz-Heilstätten, Germany.ORCID http://orcid.org/0000-0003-2874-9817
Johannes LevinDepartment of Neurology, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID http://orcid.org/0000-0001-5092-4306
Armin GieseMODAG GmbH, Wendelsheim, Germany.
Annette Janzen *Department of Neurology, Philipps-University Marburg, Marburg, Germany.
Wolfgang Hermann Oertel *Department of Neurology, Philipps-University Marburg, Marburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disease-modifying therapeutics in the α-synucleinopathies multiple system atrophy (MSA) and Parkinson's Disease (PD) are in early phases of clinical testing. Involving patients' preferences including therapy-associated risk willingness in initial stages of therapy development has been increasingly pursued in regulatory approval processes. In our study with 49 MSA and 38 PD patients, therapy-associated risk willingness was quantified using validated standard gamble scenarios for varying severities of potential drug or surgical side effects. Demonstrating a non-gaussian distribution, risk willingness varied markedly within, and between groups. MSA patients accepted a median 1% risk [interquartile range: 0.001-25%] of sudden death for a 99% [interquartile range: 99.999-75%] chance of cure, while PD patients reported a median 0.055% risk [interquartile range: 0.001-5%]. Contrary to our hypothesis, a considerable proportion of MSA patients, despite their substantially impaired quality of life, were not willing to accept increased therapy-associated risks. Satisfaction with life situation, emotional, and nonmotor disease burden were associated with MSA patients' risk willingness in contrast to PD patients, for whom age, and disease duration were associated factors. An individual approach towards MSA and PD patients is crucial as direct inference from disease (stage) to therapy-associated risk willingness is not feasible. Such studies may be considered by regulatory agencies in their approval processes assisting with the weighting of safety aspects in a patient-centric manner. A systematic quantitative assessment of patients' risk willingness and associated features may assist physicians in conducting individual consultations with patients who have MSA or PD by facilitating communication of risks and benefits of a treatment option.

Identifiers

PMID39147806
PMCPMC11327309

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