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Br J Haematol ; 198(4): 721-728, 2022 08.
Artigo em Inglês | MEDLINE | ID: mdl-35582775

RESUMO

Patients with Langerhans cell histiocytosis (LCH) may develop progressive neurodegeneration in the central nervous system (ND-CNS-LCH). Neurofilament light protein (NFL) in cerebrospinal fluid (CSF) is a promising biomarker to detect and monitor ND-CNS-LCH. We compared paired samples of NFL in plasma (p-NFL) and CSF in 10 patients (19 samples). Nine samples had abnormal CSF-NFL (defined as ≥380 ng/l) with corresponding p-NFL ≥ 2 ng/l. Ten samples had CSF-NFL < 380 ng/l; eight (80%) with p-NFL < 2 ng/l (p < 0.001; Fisher's exact test). Thus, our results suggest that p-NFL may be used to screen for ND-CNS-LCH. Further studies are encouraged, including the role of p-NFL for monitoring of ND-CNS-LCH.


Assuntos
Disfunção Cognitiva , Histiocitose de Células de Langerhans , Biomarcadores , Histiocitose de Células de Langerhans/diagnóstico , Humanos , Filamentos Intermediários , Proteínas de Neurofilamentos/líquido cefalorraquidiano
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