Data-driven subtypes show distinct glucose metabolic patterns in Parkinson’s disease, indicating potential profiling benefits.
Background Previously reported Parkinson’s disease (PD) subtyping schemes often show limited stability and cross-cohort generalizability. Objective To derive data-driven oculomotor subtypes in PD using multi-task eye-movement assessment and to characterize their cerebral glucose metabolic patterns. Methods We administered a non-invasive multi-task eye-movement battery to 122 patients with PD and 69 healthy controls. Multidimensional oculomotor features were analyzed using unsupervised k-means clustering to identify PD subtypes. In a PD subset undergoing 18 F-fluorodeoxyglucose positron emission tomography (FDG-PET; n = 30), regional cerebral glucose metabolism was quantified to compare metabolic profiles between subtypes. Results Clustering identified two PD subtypes: an oculomotor-efficient subtype (PD-E) and an oculomotor-inefficient subtype (PD-I). The subtypes differed across multiple oculomotor parameters, with antisaccade (AS) metrics showing the most prominent divergence. Compared with PD-I, PD-E showed higher FDG uptake in frontotemporal cortices. Metabolic differences were directionally concordant with groupwise patterns in cognitive measures. Conclusion Integrating eye-movement digital phenotypes with FDG-PET metabolism may provide complementary information for cognitive-domain profiling and assessment in PD. Longitudinal studies and independent cohort validation are needed to confirm stability and clinical translatability.
No takes yet. Share an insight, caveat, or question.
Zhang et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: