Worsening of myasthenic symptoms associated with statins

IF 3.6 3区 医学 Q1 CLINICAL NEUROLOGY
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Abstract

Introduction/Aims

The common presentations of statin intolerance are muscle-specific symptoms. Although statins are one type of drug reported to cause myasthenic worsening, myasthenic worsening has not been recognized as statin intolerance. The purpose of the present study is to investigate in a large cohort the safety profiles of statins in patients with myasthenia gravis (MG).

Methods

A total of 1710 consecutive patients with MG who visited sites associated with the Japan MG registry 2021 group between April and October 2021 were reviewed. Statin-associated myasthenic worsening was defined as worsening of any myasthenic symptoms on statin use and improvement of the symptom by stopping the statin or by undertaking additional treatment with patient and doctor confirmation.

Results

Among the 400 patients who used statins, 8 (2%) patients experienced statin intolerance and 6 (1.5%) patients experienced myasthenic worsening. No patients developed MG on the statin. Ptosis was a main symptom of myasthenic worsening in 4 (67%) patients. Atorvastatin was used in all patients with statin-associated myasthenic worsening. The symptoms of statin intolerance and statin-associated myasthenic worsening were improved within 2 months and 3 months, respectively, in all patients by cessation of statin use.

Discussion

Regarding statin-associated myasthenic worsening, prevalence was low, and severity was mild; with cessation of statin use, symptoms improved within a few months, and outcomes were generally good. Although statins can be used in MG patients with little concern, statin-associated myasthenic worsening should be noted in addition to the classical statin intolerance associated with statin use.

他汀类药物导致肌无力症状加重
导言/目的他汀类药物不耐受的常见表现是肌肉特异性症状。虽然他汀类药物是一种据报道会导致肌无力恶化的药物,但肌无力恶化尚未被认定为他汀类药物不耐受。本研究旨在调查他汀类药物对重症肌无力(MG)患者的安全性。方法:本研究对 2021 年 4 月至 10 月间访问日本 MG 登记 2021 小组相关站点的 1710 名连续重症肌无力患者进行了审查。结果在使用他汀类药物的 400 名患者中,有 8 名(2%)患者出现他汀类药物不耐受,6 名(1.5%)患者出现肌无力恶化。没有患者在服用他汀类药物后出现肌萎缩。上睑下垂是 4 名(67%)患者肌无力恶化的主要症状。所有出现他汀类药物相关肌无力恶化的患者都使用了阿托伐他汀。停用他汀后,所有患者的他汀不耐受症状和他汀相关肌无力恶化症状分别在2个月和3个月内得到改善。讨论关于他汀相关肌无力恶化,发病率较低,严重程度较轻;停用他汀后,症状在几个月内得到改善,疗效普遍良好。虽然他汀类药物可在MG患者中放心使用,但除了传统的他汀类药物不耐受外,还应注意他汀类药物相关肌无力恶化。
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来源期刊
Journal of the Neurological Sciences
Journal of the Neurological Sciences 医学-临床神经学
CiteScore
7.60
自引率
2.30%
发文量
313
审稿时长
22 days
期刊介绍: The Journal of the Neurological Sciences provides a medium for the prompt publication of original articles in neurology and neuroscience from around the world. JNS places special emphasis on articles that: 1) provide guidance to clinicians around the world (Best Practices, Global Neurology); 2) report cutting-edge science related to neurology (Basic and Translational Sciences); 3) educate readers about relevant and practical clinical outcomes in neurology (Outcomes Research); and 4) summarize or editorialize the current state of the literature (Reviews, Commentaries, and Editorials). JNS accepts most types of manuscripts for consideration including original research papers, short communications, reviews, book reviews, letters to the Editor, opinions and editorials. Topics considered will be from neurology-related fields that are of interest to practicing physicians around the world. Examples include neuromuscular diseases, demyelination, atrophies, dementia, neoplasms, infections, epilepsies, disturbances of consciousness, stroke and cerebral circulation, growth and development, plasticity and intermediary metabolism.
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