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富马酸二甲酯在 1 型糖尿病合并多发性硬化症患者中的应用:酮尿的重要性。

Dimethyl fumarate in a patient with multiple sclerosis and type 1 diabetes mellitus: The importance of ketonuria.

机构信息

Department of Neurology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.

Department of Children's Diabetology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.

出版信息

Mult Scler Relat Disord. 2018 Apr;21:42-45. doi: 10.1016/j.msard.2018.02.007. Epub 2018 Feb 7.

Abstract

BACKGROUND

Dimethyl fumarate (DMF) is approved for use in patients with relapsing-remitting multiple sclerosis (MS). Its mechanism of action is still not well understood, but besides the immunological pathways in MS, it may also affect the metabolism of normally functioning internal organs, tissues and cells.

CASE PRESENTATION

We report on the case of 29-year-old woman with satisfactorily-controlled type 1 diabetes (T1D), who was diagnosed as having MS. After administration of DMF she experienced intense, adverse gastro-intestinal reactions together with ketonuria up to 160 mg/dL. The highest ketone concentrations in the urine were observed approximately 2 h after each DMF dose and always with co-existing adverse reactions. Dose reduction did not improve symptoms and treatment had to be stopped. Twelve hours after the last dose of DMF all laboratory results returned to normal ranges and all gastro-intestinal adverse reactions were resolved within the following 24 h.

CONCLUSION

This is a first report of ketonuria in a MS-patient with T1D treated with DMF. Patients with MS and co-existing metabolic diseases, which are not contraindicated for DMF treatment, represent a unique opportunity to address questions regarding the possible mechanisms of action of DMF on the cellular metabolism. The use of DMF in patients with metabolic diseases needs closer attention.

摘要

背景

富马酸二甲酯 (DMF) 获批用于治疗复发缓解型多发性硬化症 (MS)。其作用机制尚未完全了解,但除了 MS 中的免疫途径外,它还可能影响正常功能的内部器官、组织和细胞的代谢。

病例介绍

我们报告了一例 29 岁的女性,患有控制良好的 1 型糖尿病 (T1D),并被诊断为患有 MS。使用 DMF 后,她出现了严重的胃肠道不良反应,同时出现了高达 160mg/dL 的酮尿症。尿液中最高的酮浓度出现在每次 DMF 剂量后约 2 小时,并且总是伴有不良反应。减少剂量并不能改善症状,因此必须停止治疗。在最后一次 DMF 剂量后 12 小时,所有实验室结果均恢复正常范围,所有胃肠道不良反应在接下来的 24 小时内得到解决。

结论

这是首例 DMF 治疗 T1D 合并 MS 的患者发生酮尿症的报告。对于合并代谢疾病但未被 DMF 治疗禁忌的 MS 患者,代表了一个探讨 DMF 对细胞代谢可能作用机制的独特机会。在代谢疾病患者中使用 DMF 需要更密切的关注。

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