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Updated: Nov 15, 2025

Rapid Fractionation and Isolation of Whole Blood Components in Samples Obtained from a Community-based Setting
Published on: November 30, 2015
Blood neurofilament light in remote settings: Alternative protocols to support sample collection in challenging
Joel Simrén1,2, Nicholas J Ashton1,3,4,5, Kaj Blennow1,2
1Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, The Sahlgrenska Academy University of Gothenburg Mölndal Sweden.
Introduction:
This study investigated alternative pre-analytical handling of blood for neurofilament light (NfL) analysis where resources are limited.
Method:
Plasma NfL was measured with single molecule array after alternative blood processing procedures: dried plasma spots (DPS), dried blood spots (DBS), and delayed 48-hour centrifugation. These were compared to standardized plasma processing (reference standard [RS]). In a discovery cohort (n = 10) and a confirmatory cohort (n = 21), whole blood was obtained from individuals with unknown clinical etiology. In the confirmatory cohort, delayed centrifugation protocol was paired with either 37°C incubation or sample shaking to test the effect of these parameters.
Results:
Delayed centrifugation (R2 = 0.991) and DPS (discovery cohort, R2 = 0.954; confirmatory cohort, DPS: R2 = 0.961) methods were strongly associated with the RS. Delayed centrifugation with higher temperatures (R2 = 0.995) and shaking (R2 = 0.975) did not affect this association. DPS (P < 0.001) returned concentrations considerably lower than the RS.
Discussion:
DPS or delayed centrifugation are viable pre-analytical procedures for the accurate quantification of plasma NfL.
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