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Low brain cholinergic activity links to freezing of gait in Parkinson's patients on medication

PET imaging shows reduced cholinergic activity in brainstem and thalamus tracks with medication-ON freezing of gait in Parkinson's, pointing beyond dopamine.

vendredi 9 octobre 2026 1 vue
Publié dans Brain
Glowing PET brain scan with highlighted brainstem and thalamus beside an elderly person's feet hesitating at a doorway

Résumé

Freezing of gait, the sudden inability to step forward, is a disabling Parkinson's symptom that sometimes persists even when dopamine medication is working. Researchers in Denmark scanned 14 Parkinson's patients with ON-state freezing using two PET tracers: one marking cholinergic nerve terminals (18F-FEOBV) and one measuring glucose metabolism (18F-FDG). They found that lower cholinergic activity in the thalamus, hippocampus, striatum, anterior cingulate and a brainstem region involved in locomotion was linked to more severe freezing and worse gait while on medication. This cholinergic pattern did not track with disease duration or general motor severity, and showed no link to freezing in the OFF state. Metabolic patterns did not correlate with freezing. The findings suggest cholinergic loss may help drive medication-ON freezing, though the sample was small.

Résumé détaillé

Gait problems, especially freezing of gait (FoG), become more common as Parkinson's disease advances and raise the risk of falls. FoG that persists despite dopamine medication is particularly troublesome because it suggests non-dopamine systems are involved. The underlying biology remains incompletely understood.

This study asked whether the brain's cholinergic system contributes. Fourteen people with Parkinson's disease and FoG in the medication ON state underwent two PET scans on separate days: 18F-FEOBV, which marks cholinergic nerve terminals, and 18F-FDG, which reflects glucose metabolism. Using principal component analysis, the team derived spatial covariance networks and correlated individual expression of these patterns with ON-state FoG, a lower body and gait subscore of the MDS-UPDRS part III, and accelerometer-based gait measures collected at home.

A cholinergic pattern correlated with ON-FoG (R² = 0.47, P = 0.045) and with other lower body and gait signs (R² = 0.79, P = 0.0077). Lower cholinergic activity in the thalamus, hippocampus, striatum, anterior cingulate and brainstem areas consistent with the mesencephalic locomotor region accompanied worse freezing and gait. This pattern was unrelated to disease duration or standard motor scores, and there was no correlation with OFF-state FoG. The metabolic pattern did not correlate with FoG, though a subset of gait symptoms showed an association.

The results support a role for cholinergic dysfunction in dopamine-resistant freezing and may help guide future therapies targeting cholinergic pathways.

Caveats are substantial: the sample was very small, there was no control group in the analysis, correlations do not prove causation, and findings need replication in larger cohorts.

Principales conclusions

  • A cholinergic PET pattern correlated with medication-ON freezing of gait (R² = 0.47, P = 0.045) in 14 Parkinson's patients.
  • Lower cholinergic activity in thalamus, hippocampus, striatum, anterior cingulate and brainstem locomotor region tracked with worse gait.
  • The cholinergic pattern was unrelated to disease duration or overall motor severity scores.
  • No cholinergic correlation was found with freezing in the OFF medication state.
  • Glucose metabolism (FDG) patterns did not correlate with freezing, though a subset of gait symptoms showed association.

Méthodologie

Cross-sectional PET imaging study of 14 Parkinson's patients with ON-state freezing of gait, scanned with 18F-FEOBV and 18F-FDG on separate days. Spatial covariance networks were derived by principal component analysis and correlated with clinical FoG ratings, a UPDRS III lower body and gait subscore, and home accelerometer gait data.

Limites de l'étude

The very small sample (n=14) and exploratory, correlational design limit statistical power and prevent causal conclusions; P-values were modest and multiple analyses were performed. Results require replication in larger, independent cohorts with comparison groups.

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