Authors
Victor Fellipe Bispo Macêdo, Alana Madeiro de Melo Barboza, Yasmin Lopes Silva Nogueira, Amanda Sena Cocivera Machado, Nilcele Freire de Oliveira
Published in
Tremor and other hyperkinetic movements (New York, N.Y.). Volume 16. Pages 40. Epub Jun 15, 2026.
Abstract
Parkinsonian tremor remains one of the least understood motor manifestations of Parkinson's disease. Unlike bradykinesia and rigidity, tremor often shows weak correlation with dopaminergic degeneration and variable responses to pharmacological and surgical treatments, suggesting mechanisms beyond classical basal ganglia dysfunction. Increasing evidence indicates that tremor may arise from interactions between multiple motor circuits rather than from a single oscillatory generator.
This mechanistic review integrates evidence from electrophysiological recordings, neuroimaging studies, lesion observations, and computational modeling studies investigating the neural mechanisms of parkinsonian tremor. Relevant literature addressing basal ganglia circuits, cerebello-thalamo-cortical pathways, and tremor-related neural oscillations was analyzed to develop a conceptual network framework.
Available evidence supports the involvement of a distributed oscillatory network in tremor generation. Within this framework, basal ganglia circuits, particularly the subthalamic nucleus-globus pallidus externa loop, act as primary oscillatory generators. Cerebello-thalamo-cortical pathways and brainstem nuclei modulate synchronization and amplitude of tremor-related activity, while thalamic nuclei function as resonance hubs integrating network oscillations and translating them into rhythmic motor output.
Conceptualizing parkinsonian tremor as a distributed network disorder helps explain several clinical observations, including the dissociation between tremor and other motor symptoms, variability in levodopa responsiveness, and heterogeneous tremor phenotypes. This framework also highlights the potential relevance of oscillatory biomarkers and network-based neuromodulation strategies, including adaptive deep brain stimulation, for future therapeutic approaches.
PMID:
42434540
Bibliographic data and abstract were imported from PubMed on 11 Jul 2026.
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