4.6 Article

Visual dysfunction is a better predictor than retinal thickness for dementia in Parkinson's disease

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BMJ PUBLISHING GROUP
DOI: 10.1136/jnnp-2023-331083

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vision; dementia; Parkinson's disease; cognition

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Visual dysfunction in Parkinson's disease predicts dementia and poor outcomes, while retinal thickness has less predictive power. This suggests that cortical structures play a role in the progression of Parkinson's dementia, and visual tests may be useful for stratification in clinical trials.
BackgroundDementia is a common and devastating symptom of Parkinson's disease (PD). Visual function and retinal structure are both emerging as potentially predictive for dementia in Parkinson's but lack longitudinal evidence. MethodsWe prospectively examined higher order vision (skew tolerance and biological motion) and retinal thickness (spectral domain optical coherence tomography) in 100 people with PD and 29 controls, with longitudinal cognitive assessments at baseline, 18 months and 36 months. We examined whether visual and retinal baseline measures predicted longitudinal cognitive scores using linear mixed effects models and whether they predicted onset of dementia, death and frailty using time-to-outcome methods. ResultsPatients with PD with poorer baseline visual performance scored lower on a composite cognitive score (beta=0.178, SE=0.05, p=0.0005) and showed greater decreases in cognition over time (beta=0.024, SE=0.001, p=0.013). Poorer visual performance also predicted greater probability of dementia (chi(2) (1)=5.2, p=0.022) and poor outcomes (chi(2) (1) =10.0, p=0.002). Baseline retinal thickness of the ganglion cell-inner plexiform layer did not predict cognitive scores or change in cognition with time in PD (beta=-0.013, SE=0.080, p=0.87; beta=0.024, SE=0.001, p=0.12). ConclusionsIn our deeply phenotyped longitudinal cohort, visual dysfunction predicted dementia and poor outcomes in PD. Conversely, retinal thickness had less power to predict dementia. This supports mechanistic models for Parkinson's dementia progression with onset in cortical structures and shows potential for visual tests to enable stratification for clinical trials.

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