Importance of cerebrospinal fluid storage conditions for the Alzheimer’s disease diagnostics on an automated platform

Author:

Ferrer Rosa1,Zhu Nuole2,Arranz Javier2,Porcel Inmaculada1,El Bounasri Shaimaa2,Sánchez Oriol2,Torres Soraya2,Julve Josep3,Lleó Alberto24,Blanco-Vaca Francisco135,Alcolea Daniel24,Tondo Mireia136ORCID

Affiliation:

1. Department of Biochemistry , Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute (IIB) Sant Pau , Barcelona , Spain

2. Sant Pau Memory Unit, Department of Neurology , Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute (IIB) Sant Pau , Barcelona , Spain

3. Center of Biomedical Investigation Network for Diabetes and Metabolic Diseases (CIBERDEM) , Madrid , Spain

4. Center of Biomedical Investigation Network for Neurodegenerative Diseases (CIBERNED) , Madrid , Spain

5. Department of Biochemistry and Molecular Biology , Universitat Autònoma de Barcelona , Barcelona , Spain

6. Comisión de Neuroquímica y Enfermedades Neurológicas, Sociedad Española de Medicina de Laboratorio , Barcelona , Spain

Abstract

Abstract Objectives Alzheimer’s disease (AD) is considered the most common cause of dementia in older people. Cerebrospinal fluid (CSF) Aβ1-42, Aβ1-40, total Tau (t-Tau), and phospho Tau (p-Tau) are important biomarkers for the diagnosis, however, they are highly dependent on the pre-analytical conditions. Our aim was to investigate the potential influence of different storage conditions on the simultaneous quantification of these biomarkers in a fully-automated platform to accommodate easier pre-analytical conditions for laboratories. Methods CSF samples were obtained from 11 consecutive patients. Aβ1-42, Aβ1-40, p-Tau, and t-Tau were quantified using the LUMIPULSE G600II automated platform. Results Temperature and storage days significantly influenced Aβ1-42 and Aβ1-40 with concentrations decreasing with days spent at 4 °C. The use of the Aβ1-42/Aβ1-40 ratio could partly compensate it. P-Tau and t-Tau were not affected by any of the tested storage conditions. For conditions involving storage at 4 °C, a correction factor of 1.081 can be applied. Diagnostic agreement was almost perfect in all conditions. Conclusions Cutoffs calculated in samples stored at −80 °C can be safely used in samples stored at −20 °C for 15–16 days or up to two days at RT and subsequent freezing at −80 °C. For samples stored at 4 °C, cutoffs would require applying a correction factor, allowing to work with the certainty of reaching the same clinical diagnosis.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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