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移植的甲基丙二酸血症患者开始使用钙调神经磷酸酶抑制剂后出现的神经毒性,包括后部可逆性脑病综合征:两例报告并文献复习

Neurotoxicity including posterior reversible encephalopathy syndrome after initiation of calcineurin inhibitors in transplanted methylmalonic acidemia patients: Two case reports and review of the literature.

作者信息

Molema Femke, Williams Monique, Langendonk Janneke, Darwish-Murad Sarwa, van de Wetering Jacqueline, Jacobs Ed, Onkenhout Willem, Brusse Esther, van der Eerden Anke, Wagenmakers Margreet

机构信息

Department of Pediatrics, Center for Lysosomal and Metabolic Disease Erasmus - Sophia Children's Hospital, University Medical Center Rotterdam The Netherlands.

Department of Internal Medicine, Erasmus University Medical Center Center for Lysosomal and Metabolic Disease Rotterdam The Netherlands.

出版信息

JIMD Rep. 2020 Jan 22;51(1):89-104. doi: 10.1002/jmd2.12088. eCollection 2020 Jan.

Abstract

INTRODUCTION

New neurological symptoms in methylmalonic acidemia (MMA) patients after liver and/or kidney transplantation (LKT) are often described as metabolic stroke-like-events. Since calcineurin inhibitors (CNIs) are a well-known cause of new neurological symptoms in non-MMA transplanted patients, we investigated the incidence of CNI-induced neurotoxicity including posterior reversible encephalopathy syndrome (PRES) in post-transplanted MMA patients.

METHODS

We report the two MMA patients treated with LKT in our center. Additionally, we performed a systematic review of case reports/series of post-transplanted MMA patients and determined if CNI-induced neurotoxicity/PRES was a likely cause of new neurological symptoms. Definite CNI-induced neurotoxicity was defined as new neurological symptoms during CNI treatment with symptom improvement after CNI dose reduction/discontinuation. PRES was defined as CNI-induced neurotoxicity with signs of vasogenic edema on brain magnetic resonance imaging (MRI)-scan post-transplantation.

RESULTS

Our two MMA patients both developed CNI-induced neurotoxicity, one had PRES. In literature, 230 transplanted MMA patients were identified. Neurological follow-up was reported in 54 of them, of which 24 were excluded from analysis since no anti-rejection medication was reported. Thirty patients, all using CNI, were included. Sixteen patients (53%) had no new neurological symptoms post-transplantation and five patients (17%) had definite CNI neurotoxicity of whom two had PRES. Including our cases this results in a pooled incidence of 22% (7/32) definite CNI neurotoxicity and 9% PRES (3/32) in post-transplanted MMA patients on CNI.

CONCLUSION

In MMA post-transplanted patients with new neurological symptoms CNI-induced neurotoxicity/PRES should be considered. Early recognition of CNI-induced neurotoxicity is essential to initiate dose reduction/discontinuation of CNI to minimize persistent neurologic damage and improve outcome.

CONCISE ONE SENTENCE TAKE HOME MESSAGE

In all post-transplanted MMA patients with new neurological symptoms CNI-induced neurotoxicity/PRES should be considered, and directly reducing the dose/discontinuation of CNI is essential.

摘要

引言

甲基丙二酸血症(MMA)患者在肝和/或肾移植(LKT)后出现的新神经症状常被描述为代谢性中风样事件。由于钙调神经磷酸酶抑制剂(CNIs)是导致非MMA移植患者出现新神经症状的常见原因,我们调查了移植后MMA患者中CNI诱导的神经毒性(包括后部可逆性脑病综合征(PRES))的发生率。

方法

我们报告了在我们中心接受LKT治疗的两名MMA患者。此外,我们对移植后MMA患者的病例报告/系列进行了系统回顾,并确定CNI诱导的神经毒性/PRES是否可能是新神经症状的原因。明确的CNI诱导的神经毒性定义为在CNI治疗期间出现新神经症状,在CNI剂量减少/停药后症状改善。PRES定义为移植后脑磁共振成像(MRI)扫描显示血管源性水肿迹象的CNI诱导的神经毒性。

结果

我们的两名MMA患者均出现了CNI诱导的神经毒性,其中一名患有PRES。在文献中,共识别出230例移植的MMA患者。其中54例报告了神经学随访情况,由于未报告抗排斥药物,其中24例被排除在分析之外。纳入了30例均使用CNI的患者。16例患者(53%)移植后无新神经症状,5例患者(17%)有明确的CNI神经毒性,其中2例患有PRES。包括我们的病例在内,这导致接受CNI治疗的移植后MMA患者中明确的CNI神经毒性合并发生率为22%(7/32),PRES为9%(3/32)。

结论

对于出现新神经症状的移植后MMA患者,应考虑CNI诱导的神经毒性/PRES。早期识别CNI诱导的神经毒性对于启动CNI剂量减少/停药以尽量减少持续性神经损伤并改善预后至关重要。

简明一句话要点

对于所有出现新神经症状的移植后MMA患者,应考虑CNI诱导的神经毒性/PRES,直接减少CNI剂量/停药至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94f7/7012740/8df05e491f3e/JMD2-51-89-g001.jpg

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