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Cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy

INTRODUCTION/AIMS: There is limited information on the potential effects of repeated intrathecal antisense oligonucleotide drug delivery on cerebrospinal fluid (CSF) biochemical and blood cell profiles. This study aimed to examine longitudinal changes in the biochemical components (glucose, protein)...

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Autores principales: Orbach, Rotem, Sagi, Liora, Sadot, Efraim, Tokatly Latzer, Itay, Shtamler, Anna, Zisberg, Tehila, Fattal‐Valevski, Aviva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828332/
https://www.ncbi.nlm.nih.gov/pubmed/36214191
http://dx.doi.org/10.1002/mus.27731
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author Orbach, Rotem
Sagi, Liora
Sadot, Efraim
Tokatly Latzer, Itay
Shtamler, Anna
Zisberg, Tehila
Fattal‐Valevski, Aviva
author_facet Orbach, Rotem
Sagi, Liora
Sadot, Efraim
Tokatly Latzer, Itay
Shtamler, Anna
Zisberg, Tehila
Fattal‐Valevski, Aviva
author_sort Orbach, Rotem
collection PubMed
description INTRODUCTION/AIMS: There is limited information on the potential effects of repeated intrathecal antisense oligonucleotide drug delivery on cerebrospinal fluid (CSF) biochemical and blood cell profiles. This study aimed to examine longitudinal changes in the biochemical components (glucose, protein) and blood cell counts in the CSF of spinal muscular atrophy (SMA) patients treated with intrathecal nusinersen. METHODS: We collected and analyzed clinical and CSF parameters (cell count, protein, glucose, culture) of 50 individuals with SMA during nusinersen treatment (22 type 1, 17 type 2, and 11 type 3). RESULTS: The median protein concentration at baseline and during treatment was within the normal range but rose during treatment and was significantly above baseline at the time of the ninth intrathecal injection (p = 0.02, two‐tailed Wilcoxon matched‐pairs test, and p = 0.0015, Friedman test for repeated measures). Further analysis showed that the increase in CSF protein concentration was evident for SMA types 2 and 3 patients, but not for type 1. This observation was also demonstrated by a significant correlation between the SMN2 gene copy number and the increase in CSF protein concentration (Spearman rank correlation test). DISCUSSION: Our results demonstrate that a delayed increase in CSF protein concentration is expected during nusinersen treatment for SMA types 2 and 3. This might reflect the medication's effect and a possible therapeutic biochemical marker.
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spelling pubmed-98283322023-01-10 Cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy Orbach, Rotem Sagi, Liora Sadot, Efraim Tokatly Latzer, Itay Shtamler, Anna Zisberg, Tehila Fattal‐Valevski, Aviva Muscle Nerve Clinical Research Short Reports INTRODUCTION/AIMS: There is limited information on the potential effects of repeated intrathecal antisense oligonucleotide drug delivery on cerebrospinal fluid (CSF) biochemical and blood cell profiles. This study aimed to examine longitudinal changes in the biochemical components (glucose, protein) and blood cell counts in the CSF of spinal muscular atrophy (SMA) patients treated with intrathecal nusinersen. METHODS: We collected and analyzed clinical and CSF parameters (cell count, protein, glucose, culture) of 50 individuals with SMA during nusinersen treatment (22 type 1, 17 type 2, and 11 type 3). RESULTS: The median protein concentration at baseline and during treatment was within the normal range but rose during treatment and was significantly above baseline at the time of the ninth intrathecal injection (p = 0.02, two‐tailed Wilcoxon matched‐pairs test, and p = 0.0015, Friedman test for repeated measures). Further analysis showed that the increase in CSF protein concentration was evident for SMA types 2 and 3 patients, but not for type 1. This observation was also demonstrated by a significant correlation between the SMN2 gene copy number and the increase in CSF protein concentration (Spearman rank correlation test). DISCUSSION: Our results demonstrate that a delayed increase in CSF protein concentration is expected during nusinersen treatment for SMA types 2 and 3. This might reflect the medication's effect and a possible therapeutic biochemical marker. John Wiley & Sons, Inc. 2022-10-19 2022-12 /pmc/articles/PMC9828332/ /pubmed/36214191 http://dx.doi.org/10.1002/mus.27731 Text en © 2022 The Authors. Muscle & Nerve published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Clinical Research Short Reports
Orbach, Rotem
Sagi, Liora
Sadot, Efraim
Tokatly Latzer, Itay
Shtamler, Anna
Zisberg, Tehila
Fattal‐Valevski, Aviva
Cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy
title Cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy
title_full Cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy
title_fullStr Cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy
title_full_unstemmed Cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy
title_short Cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy
title_sort cerebrospinal fluid characteristics of patients treated with intrathecal nusinersen for spinal muscular atrophy
topic Clinical Research Short Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828332/
https://www.ncbi.nlm.nih.gov/pubmed/36214191
http://dx.doi.org/10.1002/mus.27731
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