Evidence map›Paper›PMID 32925072›Full record

ArticleJournal of Alzheimer's disease : JAD2020

An Operational Definition of 'Abnormal Cognition' to Optimize the Prediction of Progression to Dementia: What Are Optimal Cut-Off Points for Univariate and Multivariate Normative Comparisons?

Nathalie R de Vent, Joost A Agelink van Rentergem, Hilde M Huizenga, Wiesje M van der Flier, Sieske A M Sikkes, Jaap M J Murre, Karlijn A van den Bosch, Philip Scheltens, Ben A Schmand

Abstract readComparative Study
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Nathalie R de VentBrain and Cognition, Department of Psychology, University of Amsterdam, Amsterdam, The Netherlands.
Joost A Agelink van RentergemBrain and Cognition, Department of Psychology, University of Amsterdam, Amsterdam, The Netherlands.
Hilde M HuizengaDevelopmental Psychology, Department of Psychology, University of Amsterdam, Amsterdam, The Netherlands.
Wiesje M van der FlierAlzheimer Center, Department of Neurology, VU University Medical Center, Neuroscience Campus Amsterdam, Amsterdam, The Netherlands.
Sieske A M SikkesDepartment of Epidemiology & Biostatistics, VU University Medical Center, Neuroscience Campus Amsterdam, Amsterdam, The Netherlands.
Jaap M J MurreBrain and Cognition, Department of Psychology, University of Amsterdam, Amsterdam, The Netherlands.
Karlijn A van den BoschAlzheimer Center, Department of Neurology, VU University Medical Center, Neuroscience Campus Amsterdam, Amsterdam, The Netherlands.
Philip ScheltensAlzheimer Center, Department of Neurology, VU University Medical Center, Neuroscience Campus Amsterdam, Amsterdam, The Netherlands.
Ben A SchmandBrain and Cognition, Department of Psychology, University of Amsterdam, Amsterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn neuropsychology and neurology, there is no consensus on the definition of abnormal cognition.

objectiveTo operationally define 'abnormal cognition' for optimally predicting progression to dementia in a memory clinic sample, and to test whether multivariate profile analysis of cognitive test results improves this prediction compared to standard clinical evaluation.

methodsWe used longitudinal data from 835 non-demented patients of the Amsterdam Dementia Cohort. For 10 cognitive measures at baseline, we determined which number of abnormal tests and which magnitude of score deviations best predicted progression.

resultsPredictive ability for progression to dementia of one, two, and three abnormal test scores out of 10 is highly similar (Cox hazard ratios: 3.7-4.1) provided cut-off values are adapted appropriately. Cut-offs have to be less stringent if the number of abnormal tests required increases: the optimal cut-off is z < -1.45 when one deviating score is required, z < -1.15 when two abnormal tests are required, and z < -0.70 when three abnormal tests are required. The profile analysis has similar predictive ability at the cut-off of p < 0.22 (hazard ratio 3.8). A likelihood ratio test showed that this analysis improves prediction of progression to dementia when added to standard clinical evaluation (p < 0.001).

conclusionAbnormal cognition may be defined as one, two, or three abnormal test scores out of 10 if the magnitude of score deviations is adapted accordingly. An abnormal score profile predicts decline to dementia equally well, and improves the prediction when used complimentary to standard clinical evaluation.

Indexed as

Disease ProgressionAgedCognitionCognitive DysfunctionDementiaFemaleFollow-Up StudiesHumansLongitudinal StudiesMaleMental Status and Dementia TestsMiddle AgedMultivariate AnalysisNetherlandsCognitiondementiamild cognitive impairmentmultivariate normative comparisonprofile analysis

Identifiers

PMID32925072
PMCPMC7683061

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.