A Comparison of Operational Definitions for Mild Cognitive Impairment

Author:

Polcher Alexandra12,Wolfsgruber Steffen2,Peters Oliver34,Frölich Lutz5,Wiltfang Jens678,Kornhuber Johannes9,Hüll Michael10,Rüther Eckart6,Lewczuk Piotr911,Maier Wolfgang12,Jessen Frank1213,Wagner Michael12

Affiliation:

1. Department of Neurodegenerative Diseases and Geriatric Psychiatry, University Hospital Bonn, Bonn, Germany

2. German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany

3. Department of Psychiatry and Psychotherapy, Charité, Campus Benjamin Franklin, Berlin, Germany

4. German Center for Neurodegenerative Diseases (DZNE), Berlin, Germany

5. Department of Geriatric Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany

6. Department of Psychiatry and Psychotherapy, University Medical Center Göttingen (UMG), University of Göttingen, Göttingen, Germany

7. German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany

8. iBiMED, Medical Science Department, University of Aveiro, Aveiro, Portugal

9. Department of Psychiatry and Psychotherapy, University Hospital Erlangen, and Friedrich-Alexander University of Erlangen-Nürnberg, Erlangen, Germany

10. Center for Geriatric Medicine and Gerontology, University of Freiburg, Freiburg, Germany

11. Department of Neurodegeneration Diagnostics, Medical University of Biasłystok, and Department of Biochemical Diagnostics, University Hospital of Bialystok, Bialystok, Poland

12. German Center for Neurodegenerative Diseases (DZNE), Cologne, Germany

13. Department of Psychiatry and Psychotherapy, University Hospital Cologne, Cologne, Germany

Abstract

Background: Consideration of many tests from different cognitive domains in defining mild cognitive impairment (MCI) is clinical routine, but guidelines for a neuropsychological operationalization of MCI are lacking. Objective: Among different operational MCI criteria, to identify those which are best in predicting either conversion to dementia, or a biomarker profile indicative for Alzheimer’s disease (AD). Methods: Memory clinic patients without dementia (N = 558; mean age = 66; up to 3 years of follow-up; n = 360 with baseline CSF biomarkers) were included in an observational study using most liberal criteria of cognitive impairment. Four operational definitions of MCI were retrospectively applied: 1) amnestic MCI (CERAD word list delayed recall), 2) CERAD total score, 3) comprehensive criteria and 4) base rate corrected CERAD. We compared their accuracy in predicting incident all-cause dementia or AD dementia within three years, or a concurrent CSF Aβ42/tau-ratio indicative of AD. Results: The four definitions overlapped considerably, classified 35–58% of the original sample as impaired and were associated with markedly increased PPVs regarding incident all-cause dementia (39–46% versus 26% of the original sample), AD dementia and AD biomarker positivity. The base rate corrected MCI definition had the highest prognostic accuracy. Conclusion: he operational criteria examined seem suitable to specify MCI in memory clinic settings, as they identify subjects at high risk of clinical progression. Depending on the neuropsychological battery in use, one or several of these criteria could help to calibrate the clinical judgment of test results, reduce false-positive decisions, and define risk-enriched groups for clinical trials.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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