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P100 latency of pattern reversal visual evoked potential and visual hallucination in Parkinson’s disease

M. Kohsaka, T. Oeda, A. Umemura, S. Tomita, K. Park, K. Yamamoto, H. Sugiyama, H. Sawada (Kyoto, Japan)

Meeting: 2016 International Congress

Abstract Number: 360

Keywords: Evoked potentials, Hallucinations, Parkinsonism

Session Information

Date: Monday, June 20, 2016

Session Title: Parkinson's disease: Non-motor symptoms

Session Time: 12:30pm-2:00pm

Location: Exhibit Hall located in Hall B, Level 2

Objective: To investigate whether P100 latency of pattern reversal visual evoked potential (PR-VEP) can predict the development of visual hallucination (VH) in Parkinson’s disease (PD).

Background: VH is often observed in PD, and visual dysfunction is assumed to be associated with VH, as our previous study had shown*. PR-VEP detects abnormalities in the visual pathway to the primary visual cortex. P100 component of PR-VEP originates from the lamina 2/3 in the primary visual cortex.

Methods: 99 consecutive PD patients in whom PR-VEP test had been performed were analyzed. Among them, subjects with current or previous VH at the enrollment were assigned to VH group (n=37) and subjects without VH were assigned to non-VH group (n=62). P100 latency was compared between the two groups. To elucidate whether P100 latency can predict ensuing VH development, non-VH group patients who have never developed VH (n=48) were divided into two subgroups at the median of P100 latency (110.0 msec), and a survival time analysis was performed to compare the time to VH occurrence between the subgroups.

Results: P100 latency was significantly prolonged in VH group (119.8 ± 9.1 msec) compared to those in non-VH group (110.3 ± 8.6 msec) (p<0.0001). A survival time analysis in non-VH group showed that VH occurred significantly earlier in the P100 upper half group than in the lower half group (Log-rank test p=0.0007). Cox hazard models demonstrated that P100 latency was statistically significant risk factors with age-adjusted hazard ratio of 14.3 (95% CI, 3.0-69.2).

Conclusions: P100 latency was prolonged in PD with VH, suggesting that VH was associated with the impairment of projection to the lamina 2/3 in the primary visual cortex. In addition the survival time analysis showed that extended P100 latency could be a predictor of VH in PD.

*10th International Congress on Non-Motor Dysfunctions in Parkinson’s disease and Related Disorders (Niece, 2014).

To cite this abstract in AMA style:

M. Kohsaka, T. Oeda, A. Umemura, S. Tomita, K. Park, K. Yamamoto, H. Sugiyama, H. Sawada. P100 latency of pattern reversal visual evoked potential and visual hallucination in Parkinson’s disease [abstract]. Mov Disord. 2016; 31 (suppl 2). https://www.mdsabstracts.org/abstract/p100-latency-of-pattern-reversal-visual-evoked-potential-and-visual-hallucination-in-parkinsons-disease/. Accessed May 15, 2025.
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