Background
Movement Disorder Society–Unified Parkinson's Rating Scale Part III (MDS‐UPDRS III) is the gold standard for assessing medication effects in patients with Parkinson's disease (PD). However, short and rater‐independent measurements would be ideal for future trials.
Objectives
To assess the ability of 3 different finger tapping tasks to detect levodopa/carbidopa‐induced changes over time and to determine their correlation and compare their discriminatory power with MDS‐UPDRS III.
Methods
This was a randomized, double‐blind, crossover study in 20 patients with PD receiving levodopa/carbidopa and placebo capsules after overnight medication withdrawal. Pre‐ and up to 3.5 hours postdose, MDS‐UPDRS III and tapping tasks were performed. Tasks included 2 touchscreen‐based alternate finger tapping tasks (index finger versus index–middle finger tapping) and a thumb–index finger task using a goniometer.
Results
In the alternate index finger tapping task, levodopa/carbidopa compared with placebo resulted in significantly faster (total taps: 12.5 [95% confidence interval, CI, 6.7–18.2]) and less accurate tapping (total spatial error: 240 mm [95% CI, 123–357 mm]) with improved rhythm (intertap interval standard deviation [SD], −16.3% [95% CI, −29.9% to 0.0%]). In the thumb–index finger task, tapping was significantly faster (mean opening velocity, 151 degree/s [64–237 degree/s]), with a higher mean amplitude (8.4 degrees [3.7–13.0 degrees]) and improved rhythm (intertap interval SD, −46.4% [95% CI, −63.7% to −20.9%]). The speed‐related endpoints showed a moderate‐to‐strong correlation with the MDS‐UPDRS III (r = 0.45–0.70). The effect sizes of total taps and spatial error in the alternate index finger tapping task and opening velocity in the thumb–index finger task were comparable with the MDS‐UPDRS III. In contrast, the MDS‐UPDRS III performed better than the alternate index–middle finger task.
Conclusion
The alternate index finger and the thumb–index finger tapping tasks provide short, rater‐independent measurements that are sensitive to levodopa/carbidopa effects with a similar effect size as the MDS‐UPDRS III.