Analytical aspects of molecular Alzheimer’s disease biomarkers

Author:

Andreasson Ulf1,Vanmechelen Eugeen2,Shaw Leslie M3,Zetterberg Henrik456,Vanderstichele Hugo2

Affiliation:

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

2. ADx NeuroSciences, Technologiepark 4, 9052 Gent, Belgium

3. Department of Pathology & Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

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

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

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

Abstract

In general, a biomarker has multiple uses such as a diagnostic tool and a method to monitor therapy. The quality of a biomarker depends on how big the difference is between, for example, patients and healthy controls, but also on the capacity of the method used to measure it (the uncertainty in the method should be much less than the difference between the groups). A good biomarker should also be specific towards a disease, allowing for differentiation between clinically related syndromes. In addition, it is of importance that the stability of the methods used is high enough to establish cut-off levels both in individual laboratories and on a global scale. In the field of Alzheimer’s disease, there are currently three cerebrospinal fluid markers that have been verified in multiple studies and the analytical aspects of measuring them will be discussed.

Publisher

Future Medicine Ltd

Subject

Biochemistry (medical),Clinical Biochemistry,Drug Discovery

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