Neurofilament light chain and profilin-1 dynamics in 30 spinal muscular atrophy type 3 patients treated with nusinersen.
Giulia MussoL BelloG CapeceV BozzoniL CaumoDaniele SabbatiniV ZangaroE SogusC CosmaA PetrosinoGianni SorarùM PlebaniElena PegoraroPublished in: European journal of neurology (2024)
Cerebrospinal fluid NfL levels did not qualify as an optimal surrogate treatment biomarker in adult spinal muscular atrophy patients with a long disease duration, whilst PFN-1 might to a greater extent represent lower motor neuron pathological processes. The observed biomarker level variation during the first 2 months of nusinersen treatment might suggest a limited effect on axonal remodeling or rearrangement.