Validation and attempts of revision of the MDS-recommended tests for the screening of Parkinson's disease dementia
The Movement Disorders Society (MDS) formulated diagnostic criteria and assessment guidelines for the screening of dementia in Parkinson's disease (PD). We carried out a validation of the cognitive measures suggested in the screening algorithm (i.e. the Mini Mental State Examination – MMSE – to...
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| Published in | Parkinsonism & related disorders Vol. 20; no. 1; pp. 32 - 36 |
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| Main Authors | , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
England
Elsevier Ltd
01.01.2014
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| Subjects | |
| Online Access | Get full text |
| ISSN | 1353-8020 1873-5126 1873-5126 |
| DOI | 10.1016/j.parkreldis.2013.09.008 |
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| Abstract | The Movement Disorders Society (MDS) formulated diagnostic criteria and assessment guidelines for the screening of dementia in Parkinson's disease (PD). We carried out a validation of the cognitive measures suggested in the screening algorithm (i.e. the Mini Mental State Examination – MMSE – total score, serial 7s subtraction, 3-word recall, pentagons copy, and one minute letter fluency) in 86 patients with PD. Thirty-six percent of participants were diagnosed with dementia using the MDS algorithm, but with the Dementia Rating Scale instead of the MMSE. The original MDS procedure misclassified 11 patients (12.8%) as false negatives and 3 (3.5%) as false positives, leading to 65% sensitivity and 95% specificity. The main reason for misdiagnoses was insensitivity of the MMSE total score. Three attempts were made to reach a better screening performance, which warrants high sensitivity more than high specificity: 1. exclusion of the MMSE total score as a diagnostic requirement; 2. determination of a better cut off through Receiver Operating Characteristic curve analysis; 3. replacement of the MMSE with the equally undemanding, but more PD-specific, Mini Mental Parkinson. The first two strategies generally yielded high sensitivity, but poor specificity. The best outcome was achieved using a Mini Mental Parkinson total score <27 as cognitive criterion: sensitivity was 87% and negative predictive value was 90%; however, specificity was only 67%. Our findings seem to suggest that MDS practical guidelines are specific, but might benefit from the use of more PD-oriented tools than the MMSE in terms of sensitivity. |
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| AbstractList | Abstract The Movement Disorders Society (MDS) formulated diagnostic criteria and assessment guidelines for the screening of dementia in Parkinson's disease (PD). We carried out a validation of the cognitive measures suggested in the screening algorithm (i.e. the Mini Mental State Examination – MMSE – total score, serial 7s subtraction, 3-word recall, pentagons copy, and one minute letter fluency) in 86 patients with PD. Thirty-six percent of participants were diagnosed with dementia using the MDS algorithm, but with the Dementia Rating Scale instead of the MMSE. The original MDS procedure misclassified 11 patients (12.8%) as false negatives and 3 (3.5%) as false positives, leading to 65% sensitivity and 95% specificity. The main reason for misdiagnoses was insensitivity of the MMSE total score. Three attempts were made to reach a better screening performance, which warrants high sensitivity more than high specificity: 1. exclusion of the MMSE total score as a diagnostic requirement; 2. determination of a better cut off through Receiver Operating Characteristic curve analysis; 3. replacement of the MMSE with the equally undemanding, but more PD-specific, Mini Mental Parkinson. The first two strategies generally yielded high sensitivity, but poor specificity. The best outcome was achieved using a Mini Mental Parkinson total score <27 as cognitive criterion: sensitivity was 87% and negative predictive value was 90%; however, specificity was only 67%. Our findings seem to suggest that MDS practical guidelines are specific, but might benefit from the use of more PD-oriented tools than the MMSE in terms of sensitivity. The Movement Disorders Society (MDS) formulated diagnostic criteria and assessment guidelines for the screening of dementia in Parkinson's disease (PD). We carried out a validation of the cognitive measures suggested in the screening algorithm (i.e. the Mini Mental State Examination – MMSE – total score, serial 7s subtraction, 3-word recall, pentagons copy, and one minute letter fluency) in 86 patients with PD. Thirty-six percent of participants were diagnosed with dementia using the MDS algorithm, but with the Dementia Rating Scale instead of the MMSE. The original MDS procedure misclassified 11 patients (12.8%) as false negatives and 3 (3.5%) as false positives, leading to 65% sensitivity and 95% specificity. The main reason for misdiagnoses was insensitivity of the MMSE total score. Three attempts were made to reach a better screening performance, which warrants high sensitivity more than high specificity: 1. exclusion of the MMSE total score as a diagnostic requirement; 2. determination of a better cut off through Receiver Operating Characteristic curve analysis; 3. replacement of the MMSE with the equally undemanding, but more PD-specific, Mini Mental Parkinson. The first two strategies generally yielded high sensitivity, but poor specificity. The best outcome was achieved using a Mini Mental Parkinson total score <27 as cognitive criterion: sensitivity was 87% and negative predictive value was 90%; however, specificity was only 67%. Our findings seem to suggest that MDS practical guidelines are specific, but might benefit from the use of more PD-oriented tools than the MMSE in terms of sensitivity. The Movement Disorders Society (MDS) formulated diagnostic criteria and assessment guidelines for the screening of dementia in Parkinson's disease (PD). We carried out a validation of the cognitive measures suggested in the screening algorithm (i.e. the Mini Mental State Examination - MMSE - total score, serial 7s subtraction, 3-word recall, pentagons copy, and one minute letter fluency) in 86 patients with PD. Thirty-six percent of participants were diagnosed with dementia using the MDS algorithm, but with the Dementia Rating Scale instead of the MMSE. The original MDS procedure misclassified 11 patients (12.8%) as false negatives and 3 (3.5%) as false positives, leading to 65% sensitivity and 95% specificity. The main reason for misdiagnoses was insensitivity of the MMSE total score. Three attempts were made to reach a better screening performance, which warrants high sensitivity more than high specificity: 1. exclusion of the MMSE total score as a diagnostic requirement; 2. determination of a better cut off through Receiver Operating Characteristic curve analysis; 3. replacement of the MMSE with the equally undemanding, but more PD-specific, Mini Mental Parkinson. The first two strategies generally yielded high sensitivity, but poor specificity. The best outcome was achieved using a Mini Mental Parkinson total score <27 as cognitive criterion: sensitivity was 87% and negative predictive value was 90%; however, specificity was only 67%. Our findings seem to suggest that MDS practical guidelines are specific, but might benefit from the use of more PD-oriented tools than the MMSE in terms of sensitivity.The Movement Disorders Society (MDS) formulated diagnostic criteria and assessment guidelines for the screening of dementia in Parkinson's disease (PD). We carried out a validation of the cognitive measures suggested in the screening algorithm (i.e. the Mini Mental State Examination - MMSE - total score, serial 7s subtraction, 3-word recall, pentagons copy, and one minute letter fluency) in 86 patients with PD. Thirty-six percent of participants were diagnosed with dementia using the MDS algorithm, but with the Dementia Rating Scale instead of the MMSE. The original MDS procedure misclassified 11 patients (12.8%) as false negatives and 3 (3.5%) as false positives, leading to 65% sensitivity and 95% specificity. The main reason for misdiagnoses was insensitivity of the MMSE total score. Three attempts were made to reach a better screening performance, which warrants high sensitivity more than high specificity: 1. exclusion of the MMSE total score as a diagnostic requirement; 2. determination of a better cut off through Receiver Operating Characteristic curve analysis; 3. replacement of the MMSE with the equally undemanding, but more PD-specific, Mini Mental Parkinson. The first two strategies generally yielded high sensitivity, but poor specificity. The best outcome was achieved using a Mini Mental Parkinson total score <27 as cognitive criterion: sensitivity was 87% and negative predictive value was 90%; however, specificity was only 67%. Our findings seem to suggest that MDS practical guidelines are specific, but might benefit from the use of more PD-oriented tools than the MMSE in terms of sensitivity. |
| Author | Poletti, M. Bonuccelli, U. Vista, M. Mapelli, C. De Gaspari, D. Siri, C. Appollonio, I.M. Pezzoli, G. Antonini, A. Isella, V. |
| Author_xml | – sequence: 1 givenname: V. surname: Isella fullname: Isella, V. email: valeria.isella@unimib.it organization: Neurology Section, S. Gerardo Hospital, University of Milan Bicocca, Monza, Italy – sequence: 2 givenname: C. surname: Mapelli fullname: Mapelli, C. organization: Neurology Section, S. Gerardo Hospital, University of Milan Bicocca, Monza, Italy – sequence: 3 givenname: C. surname: Siri fullname: Siri, C. organization: Parkinson Institute, Istituti Clinici di Perfezionamento, Milan, Italy – sequence: 4 givenname: D. surname: De Gaspari fullname: De Gaspari, D. organization: Parkinson Institute, Istituti Clinici di Perfezionamento, Milan, Italy – sequence: 5 givenname: G. surname: Pezzoli fullname: Pezzoli, G. organization: Parkinson Institute, Istituti Clinici di Perfezionamento, Milan, Italy – sequence: 6 givenname: A. surname: Antonini fullname: Antonini, A. organization: Parkinson Institute, Istituti Clinici di Perfezionamento, Milan, Italy – sequence: 7 givenname: M. surname: Poletti fullname: Poletti, M. organization: Department of Neuroscience, University of Pisa, Italy – sequence: 8 givenname: U. surname: Bonuccelli fullname: Bonuccelli, U. organization: Department of Neuroscience, University of Pisa, Italy – sequence: 9 givenname: M. surname: Vista fullname: Vista, M. organization: Neurology Section, Campo di Marte Hospital, Lucca, Italy – sequence: 10 givenname: I.M. surname: Appollonio fullname: Appollonio, I.M. organization: Neurology Section, S. Gerardo Hospital, University of Milan Bicocca, Monza, Italy |
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| Cites_doi | 10.1212/WNL.0b013e3181fc29c9 10.1002/mds.22877 10.1002/mds.21844 10.1155/1995/304876 10.1002/mds.24059 10.1002/mds.23322 10.1002/gps.2331 10.1097/WCO.0b013e3283168df0 10.1016/j.parkreldis.2011.05.017 10.1111/j.1532-5415.2005.53221.x 10.1001/archneur.1993.00540020018011 10.1002/mds.21507 10.1007/s00702-011-0638-1 10.1212/01.WNL.0000091864.39702.1C 10.1002/mds.23362 |
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| SubjectTerms | Aged Algorithms Dementia - diagnosis Dementia - etiology Female Humans Male MDS guidelines Mini Mental Parkinson Mini Mental State Examination Neurology Neuropsychological Tests - standards Parkinson Disease - complications Parkinson Disease - psychology Parkinson's disease dementia ROC Curve Sensitivity and Specificity |
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| Title | Validation and attempts of revision of the MDS-recommended tests for the screening of Parkinson's disease dementia |
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