Low-dose tacrolimus in treating neuromyelitis optica spectrum disorder.


Journal

Multiple sclerosis and related disorders
ISSN: 2211-0356
Titre abrégé: Mult Scler Relat Disord
Pays: Netherlands
ID NLM: 101580247

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 03 10 2020
revised: 22 11 2020
accepted: 17 12 2020
pubmed: 1 1 2021
medline: 15 5 2021
entrez: 31 12 2020
Statut: ppublish

Résumé

The value of tacrolimus (TAC) in neuromyelitis optica spectrum disorder (NMOSD) has not been fully demonstrated. In this study, we aimed to explore the effectiveness and safety of low-dose TAC in treating NMOSD. Patients with NMOSD taking low-dose TAC were retrospectively collected. We compared the annualized relapse rate (ARR) before and after the initiation of TAC. Cox proportional hazards model was used to identify the risk factors of relapse during TAC treatment with their hazard ratio (HR). The effectiveness and safety of TAC were also compared with a group of patients on mycophenolate mofetil (MMF). A total of 42 NMOSD patients taking TAC were included, with the administered dose of 1-3mg/d. The ARR (1, 0-3) after the initiation of TAC decreased significantly compared to those before TAC treatment (0, 0-2, p < 0.001). The most common adverse events (AEs) observed included alopecia (23.8%), tremor (16.7%) and elevated blood glucose (11.9%). Multivariate Cox proportional hazards model exhibited that patients with higher baseline ARR (HR: 1.77, 0.76-4.16) and Expanded Disability Status Scale (EDSS) score (HR: 1.79, 1.20-2.68) were at a higher risk for relapse during TAC treatment (p = 0.188 and 0.004, respectively). We did not observe significant difference between TAC-treated and MMF-treated patients regarding the risk of relapse (p = 0.323). Low-dose TAC was an effective and tolerable choice in treating NMOSD.

Sections du résumé

BACKGROUND BACKGROUND
The value of tacrolimus (TAC) in neuromyelitis optica spectrum disorder (NMOSD) has not been fully demonstrated. In this study, we aimed to explore the effectiveness and safety of low-dose TAC in treating NMOSD.
METHODS METHODS
Patients with NMOSD taking low-dose TAC were retrospectively collected. We compared the annualized relapse rate (ARR) before and after the initiation of TAC. Cox proportional hazards model was used to identify the risk factors of relapse during TAC treatment with their hazard ratio (HR). The effectiveness and safety of TAC were also compared with a group of patients on mycophenolate mofetil (MMF).
RESULTS RESULTS
A total of 42 NMOSD patients taking TAC were included, with the administered dose of 1-3mg/d. The ARR (1, 0-3) after the initiation of TAC decreased significantly compared to those before TAC treatment (0, 0-2, p < 0.001). The most common adverse events (AEs) observed included alopecia (23.8%), tremor (16.7%) and elevated blood glucose (11.9%). Multivariate Cox proportional hazards model exhibited that patients with higher baseline ARR (HR: 1.77, 0.76-4.16) and Expanded Disability Status Scale (EDSS) score (HR: 1.79, 1.20-2.68) were at a higher risk for relapse during TAC treatment (p = 0.188 and 0.004, respectively). We did not observe significant difference between TAC-treated and MMF-treated patients regarding the risk of relapse (p = 0.323).
CONCLUSION CONCLUSIONS
Low-dose TAC was an effective and tolerable choice in treating NMOSD.

Identifiants

pubmed: 33383362
pii: S2211-0348(20)30781-1
doi: 10.1016/j.msard.2020.102707
pii:
doi:

Substances chimiques

Immunosuppressive Agents 0
Tacrolimus WM0HAQ4WNM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102707

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Auteurs

Liang Wang (L)

Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Hongmei Tan (H)

Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Wenjuan Huang (W)

Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Jingzi ZhangBao (J)

Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Xuechun Chang (X)

Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Lei Zhou (L)

Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Chuanzhen Lu (C)

Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Min Wang (M)

Department of Ophthalmology and Vision Science, Eye and ENT Hospital, Fudan University, Shanghai, China.

Jiahong Lu (J)

Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Chongbo Zhao (C)

Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Chao Quan (C)

Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China. Electronic address: chao_quan@fudan.edu.cn.

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Classifications MeSH