Attitudes in Patients With Prodromal and Overt α ‐Synucleinopathy Toward Risk Disclosure: A Nationwide Registry
- 22 July 2026
- journal article
- research article
- Published by Wiley in Movement Disorders Clinical Practice
Abstract
Background: Identification of individuals at increased risk for synucleinopathies is becoming more feasible with advances in biomarkers. However, the ethical and practical aspects of communicating disease risk remain unresolved, particularly across diagnostic groups and cultural contexts. Objectives: We aimed to evaluate attitudes toward disclosure of future synucleinopathy risk among individuals with isolated/idiopathic REM sleep behavior disorder (iRBD), as well as in individuals who developed Parkinson's disease (PD), or multiple system atrophy (MSA), in a large non‐Western registry. Methods: This nationwide survey study included participants from 28 movement disorders and sleep centers across Türkiye. Questionnaires assessing attitudes toward risk disclosure, additional testing, and clinical trial participation were administered face‐to‐face. Responses were analyzed using contingency tables and regression models. Results are reported following the Consensus‐Based Checklist for Reporting of Survey Studies (CROSS) guideline. Results: Among 1385 participants (1039 PD, 107 MSA, 239 iRBD), individuals with iRBD showed the highest support for risk disclosure (88.3%), exceeding PD (64.4%) and MSA (51.9%). Approval declined modestly (3–8%) when framed within the absence of disease‐modifying treatment. iRBD participants were more willing for additional testing but less willing to join clinical trials (31.8%) than PD (45.3%) or MSA (48%). MSA patients expressed the greatest concern about psychological impact. Male sex had more favorable views on disclosure and trial participation, while younger and better‐educated participants favored additional testing. Conclusions: Attitudes toward risk disclosure differ markedly across the synucleinopathy spectrum and demographic characteristics. Culturally informed and diagnosis‐specific disclosure strategies will be essential for trial recruitment and patient‐centered care.Keywords
This publication has 31 references indexed in Scilit:
- Preferences regarding Disclosure of Risk for Parkinson's Disease in a Population‐based StudyMovement Disorders Clinical Practice, 2024
- Disclosing the Risk Associated with Isolated REM Behavior Disorder: The Sleep Experts’ PerspectiveMovement Disorders Clinical Practice, 2024
- Impact of sharing Alzheimer's disease biomarkers with individuals without dementia: A systematic review and meta‐analysis of empirical dataAlzheimer's & Dementia, 2023
- The heterogeneity of Parkinson’s diseaseJournal of Neural Transmission, 2023
- The Views of Patients with Isolated Rapid Eye Movement Sleep Behavior Disorder on Risk DisclosureMovement Disorders, 2023
- Challenges in the study of individuals at risk for Parkinson disease2023
- The Movement Disorder Society Criteria for the Diagnosis of Multiple System AtrophyMovement Disorders, 2022
- Risk Disclosure in Prodromal Parkinson's DiseaseMovement Disorders, 2021
- A Consensus-Based Checklist for Reporting of Survey Studies (CROSS)Journal of General Internal Medicine, 2021
- Research electronic data capture (REDCap)—A metadata-driven methodology and workflow process for providing translational research informatics supportJournal of Biomedical Informatics, 2009