Cargando…

Predictors for Therapy Response to Intrathecal Corticosteroid Therapy in Multiple Sclerosis

Objective: The autoimmune disease Multiple Sclerosis (MS) represents a heterogeneous disease pattern with an individual course that may lead to permanent disability. In addition to immuno-modulating therapies patients benefit from symptomatic approaches like intrathecal corticosteroid therapy (ICT),...

Descripción completa

Detalles Bibliográficos
Autores principales: Vohl, Katja, Duscha, Alexander, Gisevius, Barbara, Kaisler, Johannes, Gold, Ralf, Haghikia, Aiden
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395388/
https://www.ncbi.nlm.nih.gov/pubmed/30853935
http://dx.doi.org/10.3389/fneur.2019.00132
_version_ 1783399081790406656
author Vohl, Katja
Duscha, Alexander
Gisevius, Barbara
Kaisler, Johannes
Gold, Ralf
Haghikia, Aiden
author_facet Vohl, Katja
Duscha, Alexander
Gisevius, Barbara
Kaisler, Johannes
Gold, Ralf
Haghikia, Aiden
author_sort Vohl, Katja
collection PubMed
description Objective: The autoimmune disease Multiple Sclerosis (MS) represents a heterogeneous disease pattern with an individual course that may lead to permanent disability. In addition to immuno-modulating therapies patients benefit from symptomatic approaches like intrathecal corticosteroid therapy (ICT), which is frequently applied in a growing number of centers in Germany. ICT reduces spasticity, which elongates patient's walking distance and speed, thus improves quality of life. Methods: In our study we set out to investigate cerebrospinal fluid (CSF) parameters and clinical predictors for response to ICT. Therefore, we analyzed 811 CSF samples collected from 354 patients over a time period of 12 years. Patients who received ICT were divided in two groups (improving or active group) depending on their EDSS-progress. As control groups we analyzed data of ICT naïve patients, who were divided in the two groups as well. Additionally we observed the clinical progress after receiving ICT by comparison of patients in both groups. Results: The results showed clinical data had a significant influence on the probability to benefit from ICT. The probability (shown by Odds Ratio of 1.77–2.43) to belong to the improving group in contrast to the active group is significantly (p < 0.0001) higher at later stages of disease with early disease onset (< 35 years, OR = 2.43) and higher EDSS at timepoint of ICT-initiation (EDSS > 6, OR = 2.06). Additionally, we observed lower CSF cell counts (6.68 ± 1.37 μl) and lower total CSF protein (412 ± 18.25 mg/l) of patients who responded to ICT compared to patients who did not (p < 0.05). In the control group no significant differences were revealed. Furthermore analyses of our data revealed patients belonging to the improving group reach an EDSS of 6 after ICT-initiation less often than patients of the active group (after 13 years 39.8% in the improving group, 67.8% in the active group). Conclusion: Our study implies two relevant messages: (i) although the study was not designed to prospectively assess clinical data, in this cohort no severe side effects were observed under ICT; (ii) disease onset, EDSS, CSF cell count, and total protein may serve as predictive markers for therapy response.
format Online
Article
Text
id pubmed-6395388
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-63953882019-03-08 Predictors for Therapy Response to Intrathecal Corticosteroid Therapy in Multiple Sclerosis Vohl, Katja Duscha, Alexander Gisevius, Barbara Kaisler, Johannes Gold, Ralf Haghikia, Aiden Front Neurol Neurology Objective: The autoimmune disease Multiple Sclerosis (MS) represents a heterogeneous disease pattern with an individual course that may lead to permanent disability. In addition to immuno-modulating therapies patients benefit from symptomatic approaches like intrathecal corticosteroid therapy (ICT), which is frequently applied in a growing number of centers in Germany. ICT reduces spasticity, which elongates patient's walking distance and speed, thus improves quality of life. Methods: In our study we set out to investigate cerebrospinal fluid (CSF) parameters and clinical predictors for response to ICT. Therefore, we analyzed 811 CSF samples collected from 354 patients over a time period of 12 years. Patients who received ICT were divided in two groups (improving or active group) depending on their EDSS-progress. As control groups we analyzed data of ICT naïve patients, who were divided in the two groups as well. Additionally we observed the clinical progress after receiving ICT by comparison of patients in both groups. Results: The results showed clinical data had a significant influence on the probability to benefit from ICT. The probability (shown by Odds Ratio of 1.77–2.43) to belong to the improving group in contrast to the active group is significantly (p < 0.0001) higher at later stages of disease with early disease onset (< 35 years, OR = 2.43) and higher EDSS at timepoint of ICT-initiation (EDSS > 6, OR = 2.06). Additionally, we observed lower CSF cell counts (6.68 ± 1.37 μl) and lower total CSF protein (412 ± 18.25 mg/l) of patients who responded to ICT compared to patients who did not (p < 0.05). In the control group no significant differences were revealed. Furthermore analyses of our data revealed patients belonging to the improving group reach an EDSS of 6 after ICT-initiation less often than patients of the active group (after 13 years 39.8% in the improving group, 67.8% in the active group). Conclusion: Our study implies two relevant messages: (i) although the study was not designed to prospectively assess clinical data, in this cohort no severe side effects were observed under ICT; (ii) disease onset, EDSS, CSF cell count, and total protein may serve as predictive markers for therapy response. Frontiers Media S.A. 2019-02-22 /pmc/articles/PMC6395388/ /pubmed/30853935 http://dx.doi.org/10.3389/fneur.2019.00132 Text en Copyright © 2019 Vohl, Duscha, Gisevius, Kaisler, Gold and Haghikia. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Vohl, Katja
Duscha, Alexander
Gisevius, Barbara
Kaisler, Johannes
Gold, Ralf
Haghikia, Aiden
Predictors for Therapy Response to Intrathecal Corticosteroid Therapy in Multiple Sclerosis
title Predictors for Therapy Response to Intrathecal Corticosteroid Therapy in Multiple Sclerosis
title_full Predictors for Therapy Response to Intrathecal Corticosteroid Therapy in Multiple Sclerosis
title_fullStr Predictors for Therapy Response to Intrathecal Corticosteroid Therapy in Multiple Sclerosis
title_full_unstemmed Predictors for Therapy Response to Intrathecal Corticosteroid Therapy in Multiple Sclerosis
title_short Predictors for Therapy Response to Intrathecal Corticosteroid Therapy in Multiple Sclerosis
title_sort predictors for therapy response to intrathecal corticosteroid therapy in multiple sclerosis
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395388/
https://www.ncbi.nlm.nih.gov/pubmed/30853935
http://dx.doi.org/10.3389/fneur.2019.00132
work_keys_str_mv AT vohlkatja predictorsfortherapyresponsetointrathecalcorticosteroidtherapyinmultiplesclerosis
AT duschaalexander predictorsfortherapyresponsetointrathecalcorticosteroidtherapyinmultiplesclerosis
AT giseviusbarbara predictorsfortherapyresponsetointrathecalcorticosteroidtherapyinmultiplesclerosis
AT kaislerjohannes predictorsfortherapyresponsetointrathecalcorticosteroidtherapyinmultiplesclerosis
AT goldralf predictorsfortherapyresponsetointrathecalcorticosteroidtherapyinmultiplesclerosis
AT haghikiaaiden predictorsfortherapyresponsetointrathecalcorticosteroidtherapyinmultiplesclerosis