Measuring mild cognitive impairment in patients with Parkinson's disease

C Marras, MJ Armstrong, CA Meaney, S Fox… - Movement …, 2013 - Wiley Online Library
C Marras, MJ Armstrong, CA Meaney, S Fox, B Rothberg, W Reginold, DF Tang‐Wai, D Gill…
Movement Disorders, 2013Wiley Online Library
We examined the frequency of Parkinson disease with mild cognitive impairment (PD‐MCI)
and its subtypes and the accuracy of 3 cognitive scales for detecting PD‐MCI using the new
criteria for PD‐MCI proposed by the Movement Disorders Society. Nondemented patients
with Parkinson's disease completed a clinical visit with the 3 screening tests followed 1 to 3
weeks later by neuropsychological testing. Of 139 patients, 46 met Level 2 Task Force
criteria for PD‐MCI when impaired performance was based on comparisons with normative …
Abstract
We examined the frequency of Parkinson disease with mild cognitive impairment (PD‐MCI) and its subtypes and the accuracy of 3 cognitive scales for detecting PD‐MCI using the new criteria for PD‐MCI proposed by the Movement Disorders Society. Nondemented patients with Parkinson's disease completed a clinical visit with the 3 screening tests followed 1 to 3 weeks later by neuropsychological testing. Of 139 patients, 46 met Level 2 Task Force criteria for PD‐MCI when impaired performance was based on comparisons with normative scores. Forty‐two patients (93%) had multi‐domain MCI. At the lowest cutoff levels that provided at least 80% sensitivity, specificity was 44% for the Montreal Cognitive Assessment and 33% for the Scales for Outcomes in Parkinson's Disease‐Cognition. The Mini‐Mental State Examination could not achieve 80% sensitivity at any cutoff score. At the highest cutoff levels that provided specificity of at least 80%, sensitivities were low (≤44%) for all tests. When decline from estimated premorbid levels was considered evidence of cognitive impairment, 110 of 139 patients were classified with PD‐MCI, and 103 (94%) had multi‐domain MCI. We observed dramatic differences in the proportion of patients who had PD‐MCI using the new Level 2 criteria, depending on whether or not decline from premorbid level of intellectual function was considered. Recommendations for methods of operationalizing decline from premorbid levels constitute an unmet need. Among the 3 screening tests examined, none of the instruments provided good combined sensitivity and specificity for PD‐MCI. Other tests recommended by the Task Force Level 1 criteria may represent better choices, and these should be the subject of future research. © 2013 Movement Disorder Society
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