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Lymphoplasmapheresis versus plasma exchange in severe myasthenia gravis: a retrospective cohort study

BACKGROUND: Lymphoplasmapheresis (LPE) is a new therapy developed on the basis of traditional plasma exchange (PE) in combination with leukapheresis. Currently, it remains unclear whether PE and LPE show differences in efficacy for severe MG. METHODS: A retrospective analysis was conducted on 198 MG...

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Autores principales: Duan, Weiwei, Jiang, Fei, Cai, Haobing, Li, Bijuan, Ouyang, Song, Yin, Weifan, Zeng, Qiuming, Yang, Huan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10335809/
https://www.ncbi.nlm.nih.gov/pubmed/37441608
http://dx.doi.org/10.3389/fneur.2023.1212868
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author Duan, Weiwei
Jiang, Fei
Cai, Haobing
Li, Bijuan
Ouyang, Song
Yin, Weifan
Zeng, Qiuming
Yang, Huan
author_facet Duan, Weiwei
Jiang, Fei
Cai, Haobing
Li, Bijuan
Ouyang, Song
Yin, Weifan
Zeng, Qiuming
Yang, Huan
author_sort Duan, Weiwei
collection PubMed
description BACKGROUND: Lymphoplasmapheresis (LPE) is a new therapy developed on the basis of traditional plasma exchange (PE) in combination with leukapheresis. Currently, it remains unclear whether PE and LPE show differences in efficacy for severe MG. METHODS: A retrospective analysis was conducted on 198 MG patients, 75 in the PE group and 123 in the LPE group, and the patients’ Myasthenia Gravis Foundation of America (MGFA) Clinical Classification was Class IV. The treatment outcome was the change in Quantitative Myasthenia Gravis Score (QMGS) from baseline to the end of treatment. Propensity score matching (PSM) was applied for the balance of confounders between the two groups. RESULTS: In this study cohort, the safety profile of LPE and PE was good and no serious adverse events were observed. Based on PSM, 62 patients treated with LPE and 62 patients treated with PE were entered into a comparative efficacy analysis. In the PE group, patients underwent a total of 232 replacements, with a mean of 3.74. PE significantly improved the patients’ QMGS performance, with the mean QMGS decreasing from 22.98 ± 4.03 points at baseline to 18.34 ± 5.03 points after treatment, a decrease of 4.68 ± 4.04 points (p < 0.001). A decrease of ≥3 points in QMGS was considered a significant improvement, with a treatment response rate of 67.7% in the PE group. In the LPE group, patients received a total of 117 replacements, with a mean of 1.89. The patients’ mean QMGS was 23.19 ± 4.11 points at baseline and was 16.94 ± 5.78 points after treatment, a decrease of 6.26 ± 4.39 points (p < 0.001). The improvement in QMGS was more significant in patients treated with LPE compared to the PE group (p = 0.039). The treatment response rate in the LPE group was 79%, which was not significantly different compared to the PE group (p = 0.16). The LEP group had a shorter mean length of stay compared to the PE group (10.86 ± 3.96 vs. 12.14 ± 4.14 days), but the difference was not statistically significant (p = 0.13). During the 2-month follow-up period, LPE may be associated with better functional outcomes for patients, with lower QMG score and relapse rate. LPE and PE were both effective in reducing the levels of inflammatory cytokines (TNF-α, IL-1β, and IL-6) and AChR-Ab. Compared to PE, LPE was superior in the reduction of AChR-Ab titer. CONCLUSION: In severe MG, LPE may be a more preferred treatment option than PE. It achieves treatment outcomes that are not inferior to or even better than PE with fewer replacements. This study provides further evidence to support the application of LPE as a new treatment option for MG.
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spelling pubmed-103358092023-07-12 Lymphoplasmapheresis versus plasma exchange in severe myasthenia gravis: a retrospective cohort study Duan, Weiwei Jiang, Fei Cai, Haobing Li, Bijuan Ouyang, Song Yin, Weifan Zeng, Qiuming Yang, Huan Front Neurol Neurology BACKGROUND: Lymphoplasmapheresis (LPE) is a new therapy developed on the basis of traditional plasma exchange (PE) in combination with leukapheresis. Currently, it remains unclear whether PE and LPE show differences in efficacy for severe MG. METHODS: A retrospective analysis was conducted on 198 MG patients, 75 in the PE group and 123 in the LPE group, and the patients’ Myasthenia Gravis Foundation of America (MGFA) Clinical Classification was Class IV. The treatment outcome was the change in Quantitative Myasthenia Gravis Score (QMGS) from baseline to the end of treatment. Propensity score matching (PSM) was applied for the balance of confounders between the two groups. RESULTS: In this study cohort, the safety profile of LPE and PE was good and no serious adverse events were observed. Based on PSM, 62 patients treated with LPE and 62 patients treated with PE were entered into a comparative efficacy analysis. In the PE group, patients underwent a total of 232 replacements, with a mean of 3.74. PE significantly improved the patients’ QMGS performance, with the mean QMGS decreasing from 22.98 ± 4.03 points at baseline to 18.34 ± 5.03 points after treatment, a decrease of 4.68 ± 4.04 points (p < 0.001). A decrease of ≥3 points in QMGS was considered a significant improvement, with a treatment response rate of 67.7% in the PE group. In the LPE group, patients received a total of 117 replacements, with a mean of 1.89. The patients’ mean QMGS was 23.19 ± 4.11 points at baseline and was 16.94 ± 5.78 points after treatment, a decrease of 6.26 ± 4.39 points (p < 0.001). The improvement in QMGS was more significant in patients treated with LPE compared to the PE group (p = 0.039). The treatment response rate in the LPE group was 79%, which was not significantly different compared to the PE group (p = 0.16). The LEP group had a shorter mean length of stay compared to the PE group (10.86 ± 3.96 vs. 12.14 ± 4.14 days), but the difference was not statistically significant (p = 0.13). During the 2-month follow-up period, LPE may be associated with better functional outcomes for patients, with lower QMG score and relapse rate. LPE and PE were both effective in reducing the levels of inflammatory cytokines (TNF-α, IL-1β, and IL-6) and AChR-Ab. Compared to PE, LPE was superior in the reduction of AChR-Ab titer. CONCLUSION: In severe MG, LPE may be a more preferred treatment option than PE. It achieves treatment outcomes that are not inferior to or even better than PE with fewer replacements. This study provides further evidence to support the application of LPE as a new treatment option for MG. Frontiers Media S.A. 2023-06-27 /pmc/articles/PMC10335809/ /pubmed/37441608 http://dx.doi.org/10.3389/fneur.2023.1212868 Text en Copyright © 2023 Duan, Jiang, Cai, Li, Ouyang, Yin, Zeng and Yang. https://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
Duan, Weiwei
Jiang, Fei
Cai, Haobing
Li, Bijuan
Ouyang, Song
Yin, Weifan
Zeng, Qiuming
Yang, Huan
Lymphoplasmapheresis versus plasma exchange in severe myasthenia gravis: a retrospective cohort study
title Lymphoplasmapheresis versus plasma exchange in severe myasthenia gravis: a retrospective cohort study
title_full Lymphoplasmapheresis versus plasma exchange in severe myasthenia gravis: a retrospective cohort study
title_fullStr Lymphoplasmapheresis versus plasma exchange in severe myasthenia gravis: a retrospective cohort study
title_full_unstemmed Lymphoplasmapheresis versus plasma exchange in severe myasthenia gravis: a retrospective cohort study
title_short Lymphoplasmapheresis versus plasma exchange in severe myasthenia gravis: a retrospective cohort study
title_sort lymphoplasmapheresis versus plasma exchange in severe myasthenia gravis: a retrospective cohort study
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10335809/
https://www.ncbi.nlm.nih.gov/pubmed/37441608
http://dx.doi.org/10.3389/fneur.2023.1212868
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