Literature DB >> 32883119

Neurofilament light chain, a biomarker for polyneuropathy in systemic amyloidosis.

Jelger Louwsma1,2, Anne F Brunger1,2, Johan Bijzet2,3, Bart J Kroesen2,4, Wilfried W H Roeloffzen2,5, Antje Bischof6, Jens Kuhle6, Gea Drost2,7, Fiete Lange2,7, Jan B M Kuks2,7, Reinold O B Gans1,2, Bouke P C Hazenberg2,3, Hans L A Nienhuis1,2.   

Abstract

OBJECTIVE: To study serum neurofilament light chain (sNfL) in amyloid light chain (AL) amyloidosis patients with and without polyneuropathy (PNP) and to corroborate previous observations that sNfL is increased in hereditary transthyretin-related (ATTRv) amyloidosis patients with PNP.
METHODS: sNfL levels were assessed retrospectively in patients with AL amyloidosis with and without PNP (AL/PNP+ and AL/PNP-, respectively), patients with ATTRv amyloidosis and PNP (ATTRv/PNP+), asymptomatic transthyretin (TTR) gene mutation carriers (TTRv carriers) and healthy controls. Healthy controls (HC) were age- and sex-matched to both AL/PNP- (HC/AL) and TTRv carriers (HC/TTRv). The single-molecule array (Simoa) assay was used to assess sNfL levels.
RESULTS: sNfL levels were increased both in 10 AL/PNP+ patients (p < .001) and in 10 AL/PNP- patients (p < .005) compared to 10 HC/AL individuals. sNfL levels were higher in AL/PNP+ patients than in AL/PNP- patients (p < .005). sNfL levels were also increased in 15 ATTRv/PNP+ patients, compared to both 15 HC/TTRv (p < .0001) and 15 TTRv carriers (p < .0001). ATTRv/PNP+ patients with progressive PNP (PND-score > I) had the highest sNfL levels compared to patients with early PNP (PND-score I) (p = .05). sNfL levels did not differ between TTRv carriers and HC/TTRv individuals. In the group comprising all healthy controls and in the group of TTRv carriers, sNfL levels correlated with age.
CONCLUSION: sNfL levels are increased in patients with PNP in both AL and ATTRv amyloidosis and are related to severity of PNP in ATTRv amyloidosis. sNfL is a promising biomarker to detect PNP, not only in ATTRv but also in AL amyloidosis.

Entities:  

Keywords:  AL amyloidosis; ATTRv amyloidosis; Neurofilament light chain; biomarker; polyneuropathy; systemic amyloidosis

Mesh:

Substances:

Year:  2020        PMID: 32883119     DOI: 10.1080/13506129.2020.1815696

Source DB:  PubMed          Journal:  Amyloid        ISSN: 1350-6129            Impact factor:   7.141


  3 in total

1.  Patisiran in hATTR Amyloidosis: Six-Month Latency Period before Efficacy.

Authors:  Luca Gentile; Massimo Russo; Marco Luigetti; Giulia Bisogni; Andrea Di Paolantonio; Angela Romano; Valeria Guglielmino; Ilenia Arimatea; Mario Sabatelli; Antonio Toscano; Giuseppe Vita; Anna Mazzeo
Journal:  Brain Sci       Date:  2021-04-19

2.  Motor Conduction Studies and Handgrip in Hereditary TTR Amyloidosis: Simple Tools to Evaluate the Upper Limbs.

Authors:  Vincenzo Di Stefano; Ewan Thomas; Valerio Giustino; Salvatore Iacono; Angelo Torrente; Guglielmo Pillitteri; Andrea Gagliardo; Antonino Lupica; Antonio Palma; Giuseppe Battaglia; Filippo Brighina
Journal:  Front Neurol       Date:  2022-02-28       Impact factor: 4.003

Review 3.  Inherited Neuromuscular Disorders: Which Role for Serum Biomarkers?

Authors:  Antonino Lupica; Vincenzo Di Stefano; Andrea Gagliardo; Salvatore Iacono; Antonia Pignolo; Salvatore Ferlisi; Angelo Torrente; Sonia Pagano; Massimo Gangitano; Filippo Brighina
Journal:  Brain Sci       Date:  2021-03-21
  3 in total

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