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Association of free-water imaging data for the cholinergic nucleus with the motor function and subtypes in Parkinson's disease.

Front Neurol · 2025-04-04

DOI: 10.3389/fneur.2025.1477827PMID: 40255894

Open accessresearch-article; Journal ArticleOriginal source ↗

Research overview

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BackgroundDespite the importance of clinical heterogeneity in Parkinson's disease (PD), its underlying pathophysiology remains unclear.ObjectiveThis study aimed to distinguish the association of free-water (FW) imaging data for the cholinergic nuclei with the motor subtypes of PD.MethodsThe study included 150 cases of idiopathic PD from the Parkinson's Progression Markers Initiative cohort. FW imaging, including FW-corrected diffusion tensor imaging, was used to extract structural metrics from cholinergic nucleus 4 (Ch4) in the basal forebrain and the pedunculopontine nucleus. The motor subtypes were classified as tremor-dominant (TD, n = 99) and non-tremor-dominant (non-TD, n = 51). Statistical analyses were performed at baseline and the 4-year follow-up.ResultsAt baseline, FW value for Ch4 (FW-Ch4) was correlated with the tremor subscore, while FW-corrected fractional anisotropy in Ch4 (FA-t-Ch4) was negatively correlated with the rigidity subscore. However, the TD and non-TD groups showed no differences in cholinergic FW imaging data. Among the 84 patients who were followed-up, 36.36% (20/55) in the TD group and 34.48% (10/29) in the non-TD group showed a subtype shift after 4 years. Multivariate binary logistic regression analysis showed that the normalized FW value for Ch4 (nFW-Ch4) was a predictor of subtype at the 4-year follow-up (p = 0.041). In the TD subgroup, both nFW-Ch4 (p = 0.015) and normalized FW-corrected mean diffusivity in Ch4 (MD-t-Ch4) (p = 0.013) predicted subtype stability. The area under the receiver operating characteristic curve values were 0.69 and 0.73, respectively.ConclusionTremor and rigidity subscores were correlated with Ch4 FW imaging data. Moreover, Ch4 FW imaging predicted the motor subtype at the 4-year follow-up, especially identifying potential postural instability and gait difficulty (PIGD) subtype converters from the TD group.

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