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


Journal

NPJ Parkinson's disease
ISSN: 2373-8057
Titre abrégé: NPJ Parkinsons Dis
Pays: United States
ID NLM: 101675390

Informations de publication

Date de publication:
15 Aug 2024
Historique:
received: 12 10 2023
accepted: 29 07 2024
medline: 16 8 2024
pubmed: 16 8 2024
entrez: 15 8 2024
Statut: epublish

Résumé

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.

Identifiants

pubmed: 39147806
doi: 10.1038/s41531-024-00764-5
pii: 10.1038/s41531-024-00764-5
doi:

Types de publication

Journal Article

Langues

eng

Pagination

158

Informations de copyright

© 2024. The Author(s).

Références

Wenning, G. K. et al. The natural history of multiple system atrophy: a prospective European cohort study. Lancet Neurol. 12, 264–274 (2013).
doi: 10.1016/S1474-4422(12)70327-7 pubmed: 23391524 pmcid: 3581815
Vijiaratnam, N., Simuni, T., Bandmann, O., Morris, H. R. & Foltynie, T. Progress towards therapies for disease modification in Parkinson’s disease. Lancet Neurol. 20, 559–572 (2021).
doi: 10.1016/S1474-4422(21)00061-2 pubmed: 34146514
Pagano, G. et al. Trial of prasinezumab in early-stage Parkinson’s disease. N. Engl. J. Med. 387, 421–432 (2022).
doi: 10.1056/NEJMoa2202867 pubmed: 35921451
Johnson, F. R. & Zhou, M. Patient preferences in regulatory benefit-risk assessments: a US perspective. Value Health 19, 741–745 (2016).
doi: 10.1016/j.jval.2016.04.008 pubmed: 27712700
Mühlbacher, A. C., Juhnke, C., Beyer, A. R. & Garner, S. Patient-focused benefit-risk analysis to inform regulatory decisions: the european union perspective. Value Health 19, 734–740 (2016).
doi: 10.1016/j.jval.2016.04.006 pubmed: 27712699
Green, C., Brazier, J. & Deverill, M. Valuing health-related quality of life. A review of health state valuation techniques. Pharmacoeconomics 17, 151–165 (2000).
doi: 10.2165/00019053-200017020-00004 pubmed: 10947338
Gafni, A. The standard gamble method: what is being measured and how it is interpreted. Health Serv. Res. 29, 207 (1994).
pubmed: 8005790 pmcid: 1069999
Torrance, G. W. et al. Multiattribute utility function for a comprehensive health status classification system. Health Utilities Index Mark 2. Med. Care 34, 702–722 (1996).
doi: 10.1097/00005650-199607000-00004 pubmed: 8676608
Adamaszek, M. et al. Consensus paper: cerebellum and emotion. Cerebellum 16, 552–576 (2017).
doi: 10.1007/s12311-016-0815-8 pubmed: 27485952
Schmahmann, J. D. & Caplan, D. Cognition, emotion and the cerebellum. Brain 129, 290–292 (2006).
doi: 10.1093/brain/awh729 pubmed: 16434422
Glanz, B. I. et al. Risk attitudes and risk perceptions in individuals with multiple sclerosis. Mult. Scler. J. Exp. Transl. Clin. 2, 2055217316665406 (2016).
pubmed: 28607735 pmcid: 5453630
Minacapelli, E. et al. Risk attitude and personality in people with multiple sclerosis facing the choice of different disease-modifying therapy scenarios. J. Neurol. Sci. 417, 117064 (2020).
doi: 10.1016/j.jns.2020.117064 pubmed: 32763510
Fox, R. J. et al. Risk tolerance to MS therapies: survey results from the NARCOMS registry. Mult. Scler. Relat. Disord. 4, 241–249 (2015).
doi: 10.1016/j.msard.2015.03.003 pubmed: 26008941
Mansfield, C. et al. Risk tolerance in adjuvant and metastatic melanoma settings: a patient perspective study using the threshold technique. Future Oncol. 17, 2151–2167 (2021).
doi: 10.2217/fon-2020-1193 pubmed: 33709791
Kähler, K. C. et al. The outweigh of toxicity versus risk of recurrence for adjuvant interferon therapy: a survey in German melanoma patients and their treating physicians. Oncotarget 9, 26217–26225 (2018).
doi: 10.18632/oncotarget.25439 pubmed: 29899854 pmcid: 5995230
Lacy, B. E. et al. IBS patientsʼ willingness to take risks with medications. Am. J. Gastroenterol. 107, 804–809 (2012).
doi: 10.1038/ajg.2011.485 pubmed: 22664841
Hussain, A. I. et al. Eliciting patient risk willingness in clinical consultations as a means of improving decision‐making of aortic valve replacement. J. Am. Heart Assoc. 5, e002828 (2016).
Zafar, A. M., Harris, T. J., Murphy, T. P. & Machan, J. T. Patients’ perspective about risks and benefits of treatment for peripheral arterial disease. J. Vasc. Interv. Radiol. 22, 1657–1661 (2011).
doi: 10.1016/j.jvir.2011.08.027 pubmed: 22115578
Tversky, A. & Kahneman, D. The framing of decisions and the psychology of choice. Science 211, 453–458 (1981).
doi: 10.1126/science.7455683 pubmed: 7455683
McNeil, B. J., Pauker, S. G., Sox, H. C. & Tversky, A. On the elicitation of preferences for alternative therapies. N. Engl. J. Med. 306, 1259–1262 (1982).
doi: 10.1056/NEJM198205273062103 pubmed: 7070445
Gilman, S. et al. Second consensus statement on the diagnosis of multiple system atrophy. Neurology 71, 670–676 (2008).
doi: 10.1212/01.wnl.0000324625.00404.15 pubmed: 18725592 pmcid: 2676993
Postuma, R. B. & Berg, D. The new diagnostic criteria for Parkinson’s disease. Int. Rev. Neurobiol. 132, 55–78 (2017).
doi: 10.1016/bs.irn.2017.01.008 pubmed: 28554421
Dawson, N. V. et al. Health state valuation in mild to moderate cognitive impairment: feasibility of computer-based, direct patient utility assessment. Med Decis. Mak. 28, 220–232 (2008).
doi: 10.1177/0272989X07311750
Meertens, R. M. & Lion, R. Measuring an individual’s tendency to take risks: the risk propensity scale1. J. Appl. Soc. Psychol. 38, 1506–1520 (2008).
doi: 10.1111/j.1559-1816.2008.00357.x
Schrag, A. et al. Health-related quality of life in multiple system atrophy. Mov. Disord. 21, 809–815 (2006).
doi: 10.1002/mds.20808 pubmed: 16502399
Goetz, C. G. et al. Movement Disorder Society-sponsored revision of the Unified Parkinson’s Disease Rating Scale (MDS-UPDRS): scale presentation and clinimetric testing results. Mov. Disord. 23, 42 (2008).
doi: 10.1002/mds.22340
Wenning, G. K. et al. Development and validation of the Unified Multiple System Atrophy Rating Scale (UMSARS). Mov. Disord. 19, 1391–1402 (2004).
doi: 10.1002/mds.20255 pubmed: 15452868
Hoehn, M. M. & Yahr, M. D. Parkinsonism: onset, progression, and mortality. Neurology 17, 427–442 (1967).
doi: 10.1212/WNL.17.5.427 pubmed: 6067254
R Core team. R: A language and environment for statistical computing. R Foundation for Statistical Computing Vienna, Austria (2022).
Wickham, H. Ggplot2. (Springer, New York, NY, 2009). https://doi.org/10.1007/978-0-387-98141-3 .
Strobl, C., Boulesteix, A.-L., Kneib, T., Augustin, T. & Zeileis, A. Conditional variable importance for random forests. BMC Bioinform. 9, 307 (2008).
doi: 10.1186/1471-2105-9-307
Vabalas, A., Gowen, E., Poliakoff, E. & Casson, A. J. Machine learning algorithm validation with a limited sample size. PLoS ONE 14, e0224365 (2019).
doi: 10.1371/journal.pone.0224365 pubmed: 31697686 pmcid: 6837442

Auteurs

Alexander Maximilian Bernhardt (AM)

Department of Neurology, Ludwig-Maximilians-Universität München, Munich, Germany.
German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.

Marc Oeller (M)

Department for Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany. oeller@biochem.mpg.de.

Isabel Friedrich (I)

Department of Neurology, University of Leipzig Medical Center, Leipzig, Germany.

Emre Kocakavuk (E)

Department of Hematology and Stem Cell Transplantation, West German Cancer Center, University Hospital Essen, Essen, Germany.

Eliana Nachman (E)

VIB Center for Brain & Disease Research, Leuven, Belgium.
KU Leuven Department of Neurosciences, Leuven Brain Institute, Mission Lucidity, Leuven, Belgium.

Kevin Peikert (K)

Translational Neurodegeneration Section "Albrecht Kossel", Department of Neurology, University Medical Center Rostock, University of Rostock, Rostock, Germany.
Center for Transdisciplinary Neurosciences Rostock (CTNR), University Medical Center Rostock, Rostock, Germany.
United Neuroscience Campus Lund-Rostock (UNC), Rostock, Germany.

Malte Roderigo (M)

Department of Neurology with Institute of Translational Neurology, University of Muenster, Muenster, Germany.

Andreas Rossmann (A)

Department of Cardiology, Augustinum Klinik München, München, Germany.

Tabea Schröter (T)

Department of Neurology, Jena University Hospital, Jena, Germany.

Lea Olivia Wilhelm (LO)

Medical School Berlin, Berlin, Germany.

Tino Prell (T)

Department of Neurology, Jena University Hospital, Jena, Germany.
Department of Geriatrics, Halle University Hospital, Halle, Germany.

Christoph van Riesen (C)

Department of Neurology, University Medical Center Göttingen, Göttingen, Germany.
German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.

Johanna Nieweler (J)

Department of Neurology, University Medical Center Göttingen, Göttingen, Germany.

Sabrina Katzdobler (S)

Department of Neurology, Ludwig-Maximilians-Universität München, Munich, Germany.
German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.

Markus Weiler (M)

Department of Neurology, Heidelberg University Hospital, Heidelberg, Germany.

Heike Jacobi (H)

Department of Neurology, Heidelberg University Hospital, Heidelberg, Germany.

Tobias Warnecke (T)

Department of Neurology with Institute of Translational Neurology, University of Muenster, Muenster, Germany.
Department of Neurology and Neurorehabilitation, Hospital Osnabrück, Osnabrück, Germany.

Inga Claus (I)

Department of Neurology with Institute of Translational Neurology, University of Muenster, Muenster, Germany.

Carla Palleis (C)

Department of Neurology, Ludwig-Maximilians-Universität München, Munich, Germany.
German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.

Stephan Breimann (S)

German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Department of Bioinformatics, Wissenschaftszentrum Weihenstephan, Technical University of Munich, Freising, Germany.
Metabolic Biochemistry, Ludwig-Maximilians-University Munich, Munich, Germany.

Björn Falkenburger (B)

Department of Neurology, TU Dresden, Dresden, Germany.
Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Dresden, Germany.

Moritz Brandt (M)

Department of Neurology, TU Dresden, Dresden, Germany.
Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Dresden, Germany.

Andreas Hermann (A)

Translational Neurodegeneration Section "Albrecht Kossel", Department of Neurology, University Medical Center Rostock, University of Rostock, Rostock, Germany.
Center for Transdisciplinary Neurosciences Rostock (CTNR), University Medical Center Rostock, Rostock, Germany.
German Center for Neurodegenerative Diseases (DZNE), Rostock/Greifswald, Germany.

Jost-Julian Rumpf (JJ)

Department of Neurology, University of Leipzig Medical Center, Leipzig, Germany.

Joseph Claßen (J)

Department of Neurology, University of Leipzig Medical Center, Leipzig, Germany.

Günter Höglinger (G)

Department of Neurology, Ludwig-Maximilians-Universität München, Munich, Germany.
German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.

Florin Gandor (F)

Movement Disorders Clinic, Beelitz-Heilstätten, Germany.
Department of Neurology, Otto-von-Guericke University, Magdeburg, Germany.

Johannes Levin (J)

Department of Neurology, Ludwig-Maximilians-Universität München, Munich, Germany.
German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
MODAG GmbH, Wendelsheim, Germany.

Armin Giese (A)

MODAG GmbH, Wendelsheim, Germany.
Center for Neuropathology and Prion Research, Ludwig-Maximilians-University Munich, Munich, Germany.

Annette Janzen (A)

Department of Neurology, Philipps-University Marburg, Marburg, Germany.

Wolfgang Hermann Oertel (WH)

Department of Neurology, Philipps-University Marburg, Marburg, Germany.
Institute for Neurogenomics, Helmholtz Center for Environment and Health, München, Germany.

Classifications MeSH