In our study we evaluated the sensitivity and specificity of different neuropsychological tests (Addenbrooke鈥檚 Cognitive Examination, ACE; Frontal Assessment Battery, FAB and Mattis Dementia Rating Scale, MDRS) in 73 Parkinson鈥檚 disease patients without depression. By receiver operating characteristic curve analysis, these screening instruments were tested against the recently established clinical diagnostic criteria of PDD.
Best cut-off score for ACE to identify PDD was 80 points (sensitivity聽=聽74.0%, specificity聽=聽78.1%). For FAB the most optimal cut-off value was 12 points (sensitivity聽=聽66.3%, specificity聽=聽72.2%); whereas for MDRS it was 125 points (sensitivity聽=聽89.8%, specificity聽=聽98.3%). Among the examined test batteries, MDRS had the best clinicometric profile for detecting PDD.
Although the types of applied screening instruments might differ from movement disorder clinic to clinic within a country, determination of the most specific and sensitive test for the given population remains to be an important task. Our results demonstrated that the specificity and sensitivity of MDRS was better than those of ACE, FAB and MMSE in Hungary. However, further studies with larger sample size and more uniform criteria for participation are required to determine the most suitable screening instrument for cognitive impairment.