Exploratory Evaluation of the Predictive Value of Serum Neurofilament Light Chain for Autonomic Neuropathy in Hereditary Transthyretin Amyloidosis

Read full text
Authors: Milou Berends, Anne Floor Brunger, Hendrea S. A. Tingen, Johan Bijzet, Charlotte Elisabeth Teunissen, Paul A. van der Zwaag, Rijk O. B. Gans, Bouke P. C. Hazenberg, Fiete Lange, Gea Drost, Walter Noordzij, Hans L. A. Nienhuis
+1 more Riemer H. J. A. Slart
Cited by: 0

Abstract

Background/Objectives: Serum neurofilament light chain (sNfL) is a biomarker for peripheral neuropathy as sNfL correlates with polyneuropathy severity in hereditary transthyretin (ATTRv) amyloidosis. It is unclear whether sNfL also correlates with autonomic neuropathy (ANP). In this exploratory study, we aimed to evaluate the value of sNfL as marker for ANP in patients with ATTRv amyloidosis. Methods: sNfL was measured retrospectively in 10 pathogenic transthyretin gene variant (TTRv) carriers and 28 patients with ATTRv amyloidosis. All 38 individuals underwent a comprehensive evaluation for ANP. Results: Individuals with ANP had a higher median sNfL level compared to those without ANP (p < 0.001). In univariable logistic regression analysis, age-adjusted sNfL status (normal versus abnormal for age) was associated with sex, ANP, and peripheral neuropathy. In multivariable logistic regression analysis, only peripheral neuropathy significantly predicted age-adjusted sNfL status (normal versus abnormal for age), and no signal was detected for ANP. Receiver operating characteristic analysis showed a considerable area under the curve for ANP. However, the confidence interval was wide for both analyses and only four cases with isolated ANP were included. Conclusions: Therefore, in this exploratory cohort, sNfL could not be identified as a marker for ANP, and larger studies are needed to clarify its value.

Fields of Study & Subjects

Amyloidosis: Diagnosis Treatment Outcomes Hereditary Neurological Disorders Peripheral Neuropathies and Disorders

Publication details

Journal / source
Journal of Clinical Medicine
Volume
15
Issue
5
Pages
1862–1862
Publication date
28 February 2026
Language
EN