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Natalizumab Induces Changes of Cerebrospinal Fluid Measures in Multiple Sclerosis
Background: There is a lack of knowledge about the evolution of cerebrospinal fluid (CSF) markers in multiple sclerosis (MS) patients undergoing natalizumab treatment. Aim: We aimed to evaluate the effect of natalizumab on basic inflammatory CSF and MRI measures. Methods: Together, 411 patients were...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699923/ https://www.ncbi.nlm.nih.gov/pubmed/34943468 http://dx.doi.org/10.3390/diagnostics11122230 |
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author | Ganapathy Subramanian, Ranjani Horakova, Dana Vaneckova, Manuela Lorincz, Balazs Krasensky, Jan Kubala Havrdova, Eva Uher, Tomas |
author_facet | Ganapathy Subramanian, Ranjani Horakova, Dana Vaneckova, Manuela Lorincz, Balazs Krasensky, Jan Kubala Havrdova, Eva Uher, Tomas |
author_sort | Ganapathy Subramanian, Ranjani |
collection | PubMed |
description | Background: There is a lack of knowledge about the evolution of cerebrospinal fluid (CSF) markers in multiple sclerosis (MS) patients undergoing natalizumab treatment. Aim: We aimed to evaluate the effect of natalizumab on basic inflammatory CSF and MRI measures. Methods: Together, 411 patients were screened for eligibility and 93 subjects with ≥2 CSF examinations ≤6 months before and ≥12 months after natalizumab initiation were recruited. The effect of natalizumab on CSF as well as clinical and paraclinical measures was analyzed using adjusted mixed models. Results: Natalizumab induced a decrease in CSF leukocytes (p < 1 × 10(−15)), CSF protein (p = 0.00007), the albumin quotient (p = 0.007), the IgG quotient (p = 6 × 10(−15)), the IgM quotient (p = 0.0002), the IgG index (p = 0.0004), the IgM index (p = 0.003) and the number of CSF-restricted oligoclonal bands (OCBs) (p = 0.0005). CSF-restricted OCBs positivity dropped from 94.6% to 86% but 26 patients (28%) had an increased number of OCBs at the follow-up. The baseline to follow-up EDSS and T2-LV were stable; a decrease in the relapse rate was consistent with a decrease in the CSF inflammatory markers and previous knowledge about the effectiveness of natalizumab. The average annualized brain volume loss during the follow-up was −0.50% (IQR = −0.96, −0.16) and was predicted by the baseline IgM index (B = −0.37; p = 0.003). Conclusions: Natalizumab is associated with a reduction of basic CSF inflammatory measures supporting its strong anti-inflammatory properties. The IgM index at the baseline predicted future brain volume loss during the course of natalizumab treatment. |
format | Online Article Text |
id | pubmed-8699923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86999232021-12-24 Natalizumab Induces Changes of Cerebrospinal Fluid Measures in Multiple Sclerosis Ganapathy Subramanian, Ranjani Horakova, Dana Vaneckova, Manuela Lorincz, Balazs Krasensky, Jan Kubala Havrdova, Eva Uher, Tomas Diagnostics (Basel) Article Background: There is a lack of knowledge about the evolution of cerebrospinal fluid (CSF) markers in multiple sclerosis (MS) patients undergoing natalizumab treatment. Aim: We aimed to evaluate the effect of natalizumab on basic inflammatory CSF and MRI measures. Methods: Together, 411 patients were screened for eligibility and 93 subjects with ≥2 CSF examinations ≤6 months before and ≥12 months after natalizumab initiation were recruited. The effect of natalizumab on CSF as well as clinical and paraclinical measures was analyzed using adjusted mixed models. Results: Natalizumab induced a decrease in CSF leukocytes (p < 1 × 10(−15)), CSF protein (p = 0.00007), the albumin quotient (p = 0.007), the IgG quotient (p = 6 × 10(−15)), the IgM quotient (p = 0.0002), the IgG index (p = 0.0004), the IgM index (p = 0.003) and the number of CSF-restricted oligoclonal bands (OCBs) (p = 0.0005). CSF-restricted OCBs positivity dropped from 94.6% to 86% but 26 patients (28%) had an increased number of OCBs at the follow-up. The baseline to follow-up EDSS and T2-LV were stable; a decrease in the relapse rate was consistent with a decrease in the CSF inflammatory markers and previous knowledge about the effectiveness of natalizumab. The average annualized brain volume loss during the follow-up was −0.50% (IQR = −0.96, −0.16) and was predicted by the baseline IgM index (B = −0.37; p = 0.003). Conclusions: Natalizumab is associated with a reduction of basic CSF inflammatory measures supporting its strong anti-inflammatory properties. The IgM index at the baseline predicted future brain volume loss during the course of natalizumab treatment. MDPI 2021-11-29 /pmc/articles/PMC8699923/ /pubmed/34943468 http://dx.doi.org/10.3390/diagnostics11122230 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ganapathy Subramanian, Ranjani Horakova, Dana Vaneckova, Manuela Lorincz, Balazs Krasensky, Jan Kubala Havrdova, Eva Uher, Tomas Natalizumab Induces Changes of Cerebrospinal Fluid Measures in Multiple Sclerosis |
title | Natalizumab Induces Changes of Cerebrospinal Fluid Measures in Multiple Sclerosis |
title_full | Natalizumab Induces Changes of Cerebrospinal Fluid Measures in Multiple Sclerosis |
title_fullStr | Natalizumab Induces Changes of Cerebrospinal Fluid Measures in Multiple Sclerosis |
title_full_unstemmed | Natalizumab Induces Changes of Cerebrospinal Fluid Measures in Multiple Sclerosis |
title_short | Natalizumab Induces Changes of Cerebrospinal Fluid Measures in Multiple Sclerosis |
title_sort | natalizumab induces changes of cerebrospinal fluid measures in multiple sclerosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699923/ https://www.ncbi.nlm.nih.gov/pubmed/34943468 http://dx.doi.org/10.3390/diagnostics11122230 |
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