IMAJ | volume 28
Journal 2, February 2026
pages: 77-81
1 Department of Neurology and Neurosurgery, Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel
2 Department of Neurology, Sheba Medical Center, Tel Hashomer, Israel
3 Neuroimmunology Unit and Multiple Sclerosis Center, Sheba Medical Center, Tel Hashomer, Israel
4 Neuromuscular Unit, Sheba Medical Center, Tel Hashomer, Israel
5 Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel
Summary
Background:
Neurofilament light chain (NfL) is an established biomarker for detecting axonal injury in various neurological disorders. The Quanterix Single Molecule Array (Simoa) is the current standard; however, automated immunoassays, such as the Siemens Atellica and Centaur, may serve as alternatives.
Objectives:
To compare NfL measurements obtained with the Centaur system to those from the Simoa-SR-X. To assess their agreement and applicability in clinical practice, research, and animal studies.
Methods
: NfL levels were measured in 27 human serum, 8 plasma, and 16 cerebrospinal fluid (CSF) samples, and 9 murine serum samples, by Centaur and Simoa systems. NfL levels in concomitantly drawn serum and plasma were compared in 8 humans. The agreement between platforms was evaluated.
Results
: NfL levels measured by Centaur and Simoa systems demonstrated a strong correlation in serum (Spearman r=0.97,
P < 0.0001) and plasma (Pearson R²=0.95,
P < 0.0001). Centaur measurements were higher (
P = 0.01) than Simoa. Most importantly, system-specific Z-scores corrected these differences. Serum and plasma levels measured by the Centaur system correlated strongly (R²=0.98,
P < 0.0001) and showed similar results. CSF levels measured by the Centaur system were lower (52% bias) than those measured by Simoa, with poor correlation at concentrations within the normal range (R
2=0.32,
P = 0.11). Mouse serum results showed a strong correlation between systems (R²=0.86,
P < 0.001) with similar values.
Conclusions
: The Centaur system offers an alternative to Simoa for measuring NfL in human serum, plasma, and murine serum. System-specific age-adjusted Z-scores are essential for interpretation. CSF evaluation requires further assessment.