4.6 Article

Longitudinal thalamic white and grey matter changes associated with visual hallucinations in Parkinson's disease

Journal

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
Volume 93, Issue 2, Pages 169-179

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/jnnp-2021-326630

Keywords

Parkinson's disease; hallucinations

Funding

  1. Alzheimer's Research UK Clinical Research Fellowship [2018B-001]
  2. National Institute for Health Research
  3. Wellcome Clinical Research Career Development Fellowship [205167/Z/16/Z]
  4. Wellcome Trust [205167/Z/16/Z] Funding Source: Wellcome Trust

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Patients with Parkinson's disease hallucinations show significant white matter changes, particularly in posterior connections and thalamic nuclei. Cortical thickness changes are less extensive. Thalamic nucleus of the right medial mediodorsal showed both connectivity and volume loss in PD hallucinations.
Objective Visual hallucinations are common in Parkinson's disease (PD) and associated with worse outcomes. Large-scale network imbalance is seen in PD-associated hallucinations, but mechanisms remain unclear. As the thalamus is critical in controlling cortical networks, structural thalamic changes could underlie network dysfunction in PD hallucinations. Methods We used whole-brain fixel-based analysis and cortical thickness measures to examine longitudinal white and grey matter changes in 76 patients with PD (15 hallucinators, 61 non-hallucinators) and 26 controls at baseline, and after 18 months. We compared white matter and cortical thickness, adjusting for age, gender, time-between-scans and intracranial volume. To assess thalamic changes, we extracted volumes for 50 thalamic subnuclei (25 each hemisphere) and mean fibre cross-section (FC) for white matter tracts originating in each subnucleus and examined longitudinal change in PD-hallucinators versus non-hallucinators. Results PD hallucinators showed white matter changes within the corpus callosum at baseline and extensive posterior tract involvement over time. Less extensive cortical thickness changes were only seen after follow-up. White matter connections from the right medial mediodorsal magnocellular thalamic nucleus showed reduced FC in PD hallucinators at baseline followed by volume reductions longitudinally. After follow-up, almost all thalamic subnuclei showed tract losses in PD hallucinators compared with non-hallucinators. Interpretation PD hallucinators show white matter loss particularly in posterior connections and in thalamic nuclei, over time with relatively preserved cortical thickness. The right medial mediodorsal thalamic nucleus shows both connectivity and volume loss in PD hallucinations. Our findings provide mechanistic insights into the drivers of network imbalance in PD hallucinations and potential therapeutic targets.

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