Determining cut-points for Alzheimer’s disease biomarkers: statistical issues, methods and challenges

Author:

Bartlett Jonathan W12,Frost Chris12,Mattsson Niklas34,Skillbäck Tobias3,Blennow Kaj3,Zetterberg Henrik234,Schott Jonathan M5

Affiliation:

1. Centre for Statistical Methodology, London School of Hygiene & Tropical Medicine, Keppel Street, London, WC1E 7HT, UK

2. UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK

3. Institute of Neuroscience & Physiology, Department of Psychiatry & Neurochemistry, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden

4. Laboratory of Clinical Chemistry, Sahlgrenska University Hospital, S-413 45 Gothenburg, Sweden

5. UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK.

Abstract

New proposed criteria for the clinical diagnosis of Alzheimer’s disease increasingly incorporate biomarkers, most of which are normally measured on a continuous scale. Operationalizing such criteria thus requires continuous biomarkers to be dichotomized, which in turns requires the selection of a cut-point at which to dichotomize. In this article, we review the statistical principles underlying the choice of cut-points, describe some of the most commonly adopted statistical approaches used to estimate cut-points, highlight potential pitfalls in some of the approaches and characterize in what sense the estimated cut-point from each approach is optimal. We also emphasize that how a cut-point is selected must be made in reference to how the resulting dichotomized biomarker is to be used, and in particular what actions will follow from a positive or negative test result.

Publisher

Future Medicine Ltd

Subject

Biochemistry, medical,Clinical Biochemistry,Drug Discovery

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