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Establishing the Ukrainian Parkinson’s Disease Cohort within GP2: Early Results from the UPGRADE-PD Initiative

S. Bandrivska, H. Houlden, F. Magrinelli, A. Kolodii, V. Bashynska, I. Halushko, Y. Tsyoma, A. Bondarieva, A. Shevchenko, R. Svistilnik, O. Borysenko, O. Kripchak, L. Maksymova, R. Nasalyk, S. Shkrobot, I. Khubetova, A. Cherkez, P. Marushchenko, T. Slobodin (London, United Kingdom)

Meeting: 2026 International Congress

Keywords: Neurogenesis, Parkinson’s, Parkinsonism

Category: Parkinson's Disease: Epidemiology, Phenomenology, Clinical Assessment, Rating Scales

Objective: To describe the early establishment and recruitment outcomes of the Ukrainian Parkinson’s disease cohort within the Global Parkinson’s Genetics Program (GP2).

Background: Eastern European populations remain underrepresented in Parkinson’s disease (PD) genetics research. UPGRADE-PD was established to integrate Ukrainian patients into GP2 while building local movement disorders research infrastructure.

Method: Ethics approvals and material transfer agreements were completed between May and September 2025. Recruitment began in September 2025 and expanded to 13 centres through remote coordination, on-site visits, and training in standardised study procedures. Participants with PD, atypical parkinsonism, and healthy controls underwent harmonised clinical phenotyping, including MDS-UPDRS, Hoehn and Yahr staging, MoCA, PDQ-8, HADS, environmental/risk-factor questionnaires, and smell testing where available. Blood was collected from all participants, with optional cerebrospinal fluid, neuroimaging, and plasma collection where feasible. DNA samples entered the GP2 whole-genome sequencing pipeline.

Results: By 28 February 2026, 173 participants had been recruited and whole-genome sequencing initiated for 63 DNA samples. In an analysed subset of 75 participants, 55 (73.3%) had PD, 15 (20.0%) were controls, and 5 (6.7%) had atypical parkinsonian syndromes. Mean age was 58.9 years (range 36–78), and 52.0% were female. Among PD participants, tremor was the most common initial motor symptom (60.8%), followed by stiffness/frozen shoulder (21.6%) and impaired manual dexterity (19.6%). Non-motor onset features included pain, anxiety, constipation, and cognitive symptoms. Mild cognitive impairment was present in 21.0%, and 63.1% were Hoehn and Yahr stage 2–3.

Conclusion: These findings show that multicentre PD recruitment and biosample collection are feasible in Ukraine. UPGRADE-PD expands Eastern European representation in PD genetics and provides a foundation for future genomic and translational research.

To cite this abstract in AMA style:

S. Bandrivska, H. Houlden, F. Magrinelli, A. Kolodii, V. Bashynska, I. Halushko, Y. Tsyoma, A. Bondarieva, A. Shevchenko, R. Svistilnik, O. Borysenko, O. Kripchak, L. Maksymova, R. Nasalyk, S. Shkrobot, I. Khubetova, A. Cherkez, P. Marushchenko, T. Slobodin. Establishing the Ukrainian Parkinson’s Disease Cohort within GP2: Early Results from the UPGRADE-PD Initiative [abstract]. Mov Disord. 2026; 41 (suppl 1). https://www.mdsabstracts.org/abstract/establishing-the-ukrainian-parkinsons-disease-cohort-within-gp2-early-results-from-the-upgrade-pd-initiative/. Accessed October 1, 2026.
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