Suppr超能文献

肿瘤坏死因子-α阻滞剂治疗期间发生的脱髓鞘性神经病的长期病程。

Long-term course of demyelinating neuropathies occurring during tumor necrosis factor-alpha-blocker therapy.

作者信息

Lozeron Pierre, Denier Christian, Lacroix Catherine, Adams David

机构信息

Department of Neurology, Assistance Publique-Hôpitaux de Paris, Université Paris Sud, France.

出版信息

Arch Neurol. 2009 Apr;66(4):490-7. doi: 10.1001/archneurol.2009.11.

Abstract

OBJECTIVE

To report the long-term follow-up (mean, 41 months; range, 25-55 months) of patients with demyelinating neuropathy occurring after tumor necrosis factor-alpha (TNF-alpha) blocker treatment (infliximab [Remicade], etanercept [Enbrel], and adalimumab [Humira]).

BACKGROUND

Demyelinating neuropathy is a rare adverse event of anti-TNF-alpha therapy. Improvement usually occurs after drug interruption and/or in association with usual treatments for demyelinating neuropathies.

DESIGN

Case report with review of the previously published cases.

SETTING

University hospital in Le Kremlin-Bicêtre, France: tertiary reference center for peripheral neuropathies and national reference center for rare peripheral neuropathies (www.nnerf.fr).

PATIENTS

Five patients (4 men, mean age, 47 years) who developed a demyelinating neuropathy during anti-TNF-alpha therapy.

MAIN OUTCOME MEASURE

Development of neuropathy.

RESULTS

Neuropathy developed early (8 months) after treatment introduction. Various clinical patterns were encountered, including pure sensory neuropathy. Immunomodulating treatments were always required for neuropathy control. Chronic demyelinating neuropathy developed either after change of anti-TNF-alpha drug or spontaneously after treatment discontinuation without any drug reintroduction.

CONCLUSION

Influence of anti-TNF-alpha treatment continuation on the long-term course of neuropathy is variable, suggesting that anti-TNF-alpha treatment withdrawal is not always necessary for neuropathy control.

摘要

目的

报告肿瘤坏死因子-α(TNF-α)阻滞剂治疗(英夫利昔单抗[类克]、依那西普[恩利]和阿达木单抗[修美乐])后发生脱髓鞘性神经病患者的长期随访情况(平均41个月;范围25 - 55个月)。

背景

脱髓鞘性神经病是抗TNF-α治疗的一种罕见不良事件。通常在停药和/或联合脱髓鞘性神经病的常规治疗后病情改善。

设计

病例报告并回顾既往发表的病例。

地点

法国克里姆林-比塞特大学医院:周围神经病三级转诊中心及罕见周围神经病国家转诊中心(www.nnerf.fr)。

患者

5例患者(4例男性,平均年龄47岁),在抗TNF-α治疗期间发生脱髓鞘性神经病。

主要观察指标

神经病的发生。

结果

神经病在开始治疗后早期(8个月)出现。出现了多种临床类型,包括纯感觉性神经病。控制神经病始终需要免疫调节治疗。慢性脱髓鞘性神经病在更换抗TNF-α药物后或停药且未重新用药后自发出现。

结论

继续抗TNF-α治疗对神经病长期病程的影响不一,提示控制神经病不一定总是需要停用抗TNF-α治疗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验