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Nusinersen in type 0 spinal muscular atrophy: should we treat?

A male infant affected by type 0 SMA with one copy of SMN2 received early treatment with Nusinersen at the age of 13 days. He showed mild motor improvement 2 months after treatment started but despite also showing some minimal respiratory improvement, required tracheostomy at the age of 4 months and...

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Autores principales: Tiberi, Eloisa, Costa, Simonetta, Pane, Marika, Priolo, Francesca, de Sanctis, Roberto, Romeo, Domenico, Tiziano, Francesco D., Conti, Giorgio, Vento, Giovanni, Mercuri, Eugenio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732235/
https://www.ncbi.nlm.nih.gov/pubmed/33147378
http://dx.doi.org/10.1002/acn3.51126
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author Tiberi, Eloisa
Costa, Simonetta
Pane, Marika
Priolo, Francesca
de Sanctis, Roberto
Romeo, Domenico
Tiziano, Francesco D.
Conti, Giorgio
Vento, Giovanni
Mercuri, Eugenio
author_facet Tiberi, Eloisa
Costa, Simonetta
Pane, Marika
Priolo, Francesca
de Sanctis, Roberto
Romeo, Domenico
Tiziano, Francesco D.
Conti, Giorgio
Vento, Giovanni
Mercuri, Eugenio
author_sort Tiberi, Eloisa
collection PubMed
description A male infant affected by type 0 SMA with one copy of SMN2 received early treatment with Nusinersen at the age of 13 days. He showed mild motor improvement 2 months after treatment started but despite also showing some minimal respiratory improvement, required tracheostomy at the age of 4 months and had increasing cardiac and autonomic dysfunction leading to exitus at 5 months. Our findings, expanding the results available on Nusinersen, confirm its relative efficacy in the most severely affected infants and provide clinical evidence to be used at the time requests for treating severe infants are discussed.
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spelling pubmed-77322352020-12-16 Nusinersen in type 0 spinal muscular atrophy: should we treat? Tiberi, Eloisa Costa, Simonetta Pane, Marika Priolo, Francesca de Sanctis, Roberto Romeo, Domenico Tiziano, Francesco D. Conti, Giorgio Vento, Giovanni Mercuri, Eugenio Ann Clin Transl Neurol Case Study A male infant affected by type 0 SMA with one copy of SMN2 received early treatment with Nusinersen at the age of 13 days. He showed mild motor improvement 2 months after treatment started but despite also showing some minimal respiratory improvement, required tracheostomy at the age of 4 months and had increasing cardiac and autonomic dysfunction leading to exitus at 5 months. Our findings, expanding the results available on Nusinersen, confirm its relative efficacy in the most severely affected infants and provide clinical evidence to be used at the time requests for treating severe infants are discussed. John Wiley and Sons Inc. 2020-11-04 /pmc/articles/PMC7732235/ /pubmed/33147378 http://dx.doi.org/10.1002/acn3.51126 Text en © 2020 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Study
Tiberi, Eloisa
Costa, Simonetta
Pane, Marika
Priolo, Francesca
de Sanctis, Roberto
Romeo, Domenico
Tiziano, Francesco D.
Conti, Giorgio
Vento, Giovanni
Mercuri, Eugenio
Nusinersen in type 0 spinal muscular atrophy: should we treat?
title Nusinersen in type 0 spinal muscular atrophy: should we treat?
title_full Nusinersen in type 0 spinal muscular atrophy: should we treat?
title_fullStr Nusinersen in type 0 spinal muscular atrophy: should we treat?
title_full_unstemmed Nusinersen in type 0 spinal muscular atrophy: should we treat?
title_short Nusinersen in type 0 spinal muscular atrophy: should we treat?
title_sort nusinersen in type 0 spinal muscular atrophy: should we treat?
topic Case Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732235/
https://www.ncbi.nlm.nih.gov/pubmed/33147378
http://dx.doi.org/10.1002/acn3.51126
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