Preanalytical stability of plasma biomarkers for Alzheimer's disease pathology

Author:

Sunde Anita L.12ORCID,Alsnes Ingvild V.3,Aarsland Dag14,Ashton Nicholas J.1567,Tovar‐Rios Diego A.189,De Santis Giovanni5,Blennow Kaj5,Zetterberg Henrik510111213,Kjosavik Svein R.14

Affiliation:

1. Centre for Age‐Related Medicine (SESAM) Stavanger University Hospital Stavanger Norway

2. Department of Clinical Medicine University of Bergen Bergen Norway

3. Department of Public Health University of Stavanger Stavanger Norway

4. Department of Old Age Psychiatry Institute of Psychiatry Psychology and Neuroscience King's College London UK

5. Department of Psychiatry and Neurochemistry Institute of Neuroscience & Physiology the Sahlgrenska Academy at the University of Gothenburg Mölndal Sweden

6. King's College London Institute of Psychiatry Psychology and Neuroscience Maurice Wohl Institute Clinical Neuroscience Institute London London UK

7. NIHR Biomedical Research Centre for Mental Health & Biomedical Research Unit for Dementia at South London & Maudsley NHS Foundation London UK

8. Faculty of Health Sciences University of Stavanger Stavanger Norway

9. Grupo INFERIR Facultad de Ingeniería Universidad del Valle Santiago de Cali Valle del Cauca Colombia

10. Clinical Neurochemistry Laboratory Sahlgrenska University Hospital Mölndal Sweden

11. Department of Neurodegenerative Disease UCL Institute of Neurology London UK

12. UK Dementia Research Institute at UCL London UK

13. Hong Kong Center for Neurodegenerative Diseases Hong Kong China

14. The General Practice and Care Coordination Research Group Stavanger University Hospital Stavanger Norway

Abstract

AbstractIntroductionPlasma tests have demonstrated high diagnostic accuracy for identifying Alzheimer's disease pathology. To facilitate the transition to clinical utility, we assessed whether plasma storage duration and temperature affect the biomarker concentrations.MethodsPlasma samples from 13 participants were stored at +4°C and +18°C. Concentrations of six biomarkers were measured after 2, 4, 6, 8, 10, and 24 h by single molecule array assays.ResultsPhosphorylated tau 181 (p‐tau181), phosphorylated tau 231 (p‐tau231), neurofilament light (NfL), and glial fibrillary acidic protein (GFAP) concentrations were unchanged both when stored at +4°C and +18°C. Amyloid‐β 40 (Aβ40) and amyloid‐β 42 (Aβ42) concentrations were stable for 24 h at +4°C but declined when stored at +18°C for longer than 6 h. This decline did not affect the Aβ42/Aβ40 ratio.DiscussionPlasma samples can be stored for 24 h at +4°C or +18°C and result in valid assay results for p‐tau181, p‐tau231, Aβ42/Aβ40 ratio, GFAP, and NfL.HIGHLIGHTS Plasma samples were stored for 24 h at +4°C and +18°C, mimicking clinical practice. Concentrations for Alzheimer's disease biomarkers were measured at six time‐points. p‐tau181, p‐tau231, NfL, and GFAP concentrations were unchanged during the experiment. Storage at +18°C affected Aβ40 and Aβ42 concentrations while storage at +4°C did not. The Aβ42/Aβ40 ratio was unaffected. These plasma tests seem suitable for use in general practice.

Funder

Helse Vest

Publisher

Wiley

Subject

Psychiatry and Mental health,Neurology (clinical)

Reference21 articles.

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