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Pathophysiology of Chronic Inflammatory Demyelinating Polyneuropathy: Insights into Classification and Therapeutic Strategy.慢性炎症性脱髓鞘性多发性神经病的病理生理学:对分类和治疗策略的见解
Neurol Ther. 2020 Dec;9(2):213-227. doi: 10.1007/s40120-020-00190-8. Epub 2020 May 14.
2
History, Diagnosis, and Management of Chronic Inflammatory Demyelinating Polyradiculoneuropathy.慢性炎症性脱髓鞘性多发性神经根神经病的历史、诊断和治疗。
Mayo Clin Proc. 2018 Jun;93(6):777-793. doi: 10.1016/j.mayocp.2018.03.026.
3
Tacrolimus: An updated review on delivering strategies for multifarious diseases.他克莫司:一种用于多种疾病的新型给药策略的更新综述。
Eur J Pharm Sci. 2018 Mar 1;114:217-227. doi: 10.1016/j.ejps.2017.12.017. Epub 2017 Dec 22.
4
Unconventional treatments for chronic inflammatory demyelinating polyneuropathy.慢性炎症性脱髓鞘性多发性神经病的非常规治疗方法。
Neurodegener Dis Manag. 2017 Oct;7(5):331-342. doi: 10.2217/nmt-2017-0017. Epub 2017 Oct 18.
5
Tacrolimus confers lower acute rejection rates and better renal allograft survival compared to cyclosporine.与环孢素相比,他克莫司可降低急性排斥反应发生率,并提高肾移植存活率。
World J Transplant. 2016 Dec 24;6(4):697-702. doi: 10.5500/wjt.v6.i4.697.
6
Late onset tacrolimus-induced life-threatening polyneuropathy in a kidney transplant recipient patient.一名肾移植受者患者出现迟发性他克莫司诱导的危及生命的多发性神经病。
Clin Kidney J. 2012 Aug;5(4):323-6. doi: 10.1093/ckj/sfs067.
7
Use of antioxidants to prevent cyclosporine a toxicity.使用抗氧化剂预防环孢素 A 毒性。
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8
Immunomodulatory treatment other than corticosteroids, immunoglobulin and plasma exchange for chronic inflammatory demyelinating polyradiculoneuropathy.除皮质类固醇、免疫球蛋白和血浆置换外,用于慢性炎性脱髓鞘性多发性神经根神经病的免疫调节治疗
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9
European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society - first revision.欧洲神经病学会联合会/周围神经学会关于慢性炎症性脱髓鞘性多发性神经病管理指南:欧洲神经病学会联合会和周围神经学会联合工作组的报告-第一版修订。
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10
Chronic inflammatory demyelinating polyradiculoneuropathy: diagnostic and therapeutic challenges for a treatable condition.慢性炎症性脱髓鞘性多发性神经病:一种可治疗疾病的诊断和治疗挑战。
Lancet Neurol. 2010 Apr;9(4):402-12. doi: 10.1016/S1474-4422(10)70041-7.

他克莫司治疗复发缓解型慢性炎症性脱髓鞘性多发性神经根神经病:两例报告。

Tacrolimus treatment for relapsing-remitting chronic inflammatory demyelinating polyradiculoneuropathy: Two case reports.

作者信息

Zhu Wen-Jia, Da Yu-Wei, Chen Hai, Xu Min, Lu Yan, Di Li, Duo Jian-Ying

机构信息

Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China.

出版信息

World J Clin Cases. 2022 Feb 16;10(5):1709-1715. doi: 10.12998/wjcc.v10.i5.1709.

DOI:10.12998/wjcc.v10.i5.1709
PMID:35211613
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8855276/
Abstract

BACKGROUND

This study describes the efficacy of a tacrolimus treatment regimen used to treat two patients with relapsing-remitting chronic inflammatory demyelinating polyradiculoneuropathy (CIDP).

CASE SUMMARY

Two patients (17-year-old female and 27-year-old male) were enrolled in the current study and were followed up for 12 mo. The first patient was administered tacrolimus (2 mg/d) for 12 mo and prednisolone (40 mg/d) for six months. The second patient was administered tacrolimus (3 mg/d) for six months. Both patients were followed up for 12 mo and the degree of recurrent weakness or normalized motor function was monitored. In addition, nerve conduction studies and tacrolimus levels were recorded. Following tacrolimus treatment, both patients showed marked improvement in clinical outcomes. In the first patient, prednisolone treatment was successfully withdrawn after six months. Sensory as well as motor nerve conduction velocities showed evident recovery following treatment. However, conduction velocities did not completely return to normal, suggesting that electrophysiological recovery can be slower than clinical recovery.

CONCLUSION

Neither patient exhibited any adverse effects due to the tacrolimus therapy. Therefore, tacrolimus can be effective for the treatment of patients with steroid-resistant CIDP.

摘要

背景

本研究描述了一种他克莫司治疗方案用于治疗两名复发缓解型慢性炎性脱髓鞘性多发性神经根神经病(CIDP)患者的疗效。

病例总结

两名患者(17岁女性和27岁男性)纳入本研究并随访12个月。第一名患者接受他克莫司(2mg/d)治疗12个月,泼尼松龙(40mg/d)治疗6个月。第二名患者接受他克莫司(3mg/d)治疗6个月。两名患者均随访12个月,监测复发肌无力程度或运动功能恢复正常情况。此外,记录神经传导研究和他克莫司血药浓度。他克莫司治疗后,两名患者临床结局均显著改善。第一名患者在6个月后成功停用泼尼松龙。治疗后感觉及运动神经传导速度均有明显恢复。然而,传导速度未完全恢复正常,提示电生理恢复可能慢于临床恢复。

结论

两名患者均未出现他克莫司治疗相关的不良反应。因此,他克莫司对类固醇抵抗型CIDP患者可能有效。