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Nusinersen Induces Disease-Severity-Specific Neurometabolic Effects in Spinal Muscular Atrophy

Authors :
Francesco Errico
Carmen Marino
Manuela Grimaldi
Tommaso Nuzzo
Valentina Bassareo
Valeria Valsecchi
Chiara Panicucci
Elia Di Schiavi
Tommaso Mazza
Claudio Bruno
Adele D’Amico
Manolo Carta
Anna Maria D’Ursi
Enrico Bertini
Livio Pellizzoni
Alessandro Usiello
Errico, Francesco
Marino, Carmen
Grimaldi, Manuela
Nuzzo, Tommaso
Bassareo, Valentina
Valsecchi, Valeria
Panicucci, Chiara
Di Schiavi, Elia
Mazza, Tommaso
Bruno, Claudio
D'Amico, Adele
Carta, Manolo
D'Ursi, Anna Maria
Bertini, Enrico
Pellizzoni, Livio
Usiello, Alessandro
D’Amico, Adele
Maria D’Ursi, Anna
Source :
Biomolecules; Volume 12; Issue 10; Pages: 1431
Publication Year :
2022

Abstract

Intrathecal delivery of Nusinersen–an antisense oligonucleotide that promotes survival motor neuron (SMN) protein induction–is an approved therapy for spinal muscular atrophy (SMA). Here, we employed nuclear magnetic resonance (NMR) spectroscopy to longitudinally characterize the unknown metabolic effects of Nusinersen in the cerebrospinal fluid (CSF) of SMA patients across disease severity. Modulation of amino acid metabolism is a common denominator of biochemical changes induced by Nusinersen, with distinct downstream metabolic effects according to disease severity. In severe SMA1 patients, Nusinersen stimulates energy-related glucose metabolism. In intermediate SMA2 patients, Nusinersen effects are also related to energy homeostasis but involve ketone body and fatty acid biosynthesis. In milder SMA3 patients, Nusinersen mainly modulates amino acid metabolism. Moreover, Nusinersen modifies the CSF metabolome of a more severe clinical group towards the profile of untreated SMA patients with milder disease. These findings reveal disease severity-specific neurometabolic signatures of Nusinersen treatment, suggesting a selective modulation of peripheral organ metabolism by this CNS-directed therapy in severe SMA patients.

Details

Language :
English
Database :
OpenAIRE
Journal :
Biomolecules; Volume 12; Issue 10; Pages: 1431
Accession number :
edsair.doi.dedup.....971cdcfad0d1479e9bd40479c3078dea