{"title":"The mortality of myasthenia gravis with myocarditis: A single-center retrospective study","authors":"Nana Zhang , Hongxi Chen , Rui Wang, Hongyu Zhou","doi":"10.1016/j.jns.2025.123440","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>While numerous studies have investigated the onset features of myasthenia gravis (MG) complicated with myocarditis, there are few articles focusing on the prognosis of patients with both diseases. This study aims to examine mortality in patients with MG who also have myocarditis, and to summarize the clinical characteristics of deceased patients with both conditions.</div></div><div><h3>Results</h3><div>A total of 91 patients with MG were included in our study, of which 19 (20.9 %) were diagnosed with myocarditis. Shorter MG duration, thymoma, history of myasthenia crisis (MC) and use of immune checkpoint inhibitors (ICIs) were risk factors for developing myocarditis in MG patients. Among the 13 myocarditis-MG patients who did not receive ICIs, 11(84.6 %) had thymoma and 5 (71.4 %) of the 7 tested were positive for titin-IgG. In all myocarditis-MG patients, 11 (57.9 %) died from myocarditis (average age 51 ± 18 years), with 9 (81.8 %) having thymoma and 5 (45 %) having a history of myasthenia crisis. Compared to the mortality rates of MC patients (16.1 %) and the general MG patients (1.8 %), the mortality rate of myocarditis-MG patients is significantly higher.</div></div><div><h3>Conclusions</h3><div>The study highlights that MG patients with myocarditis face a significantly increased risk of mortality. Thymoma and a history of MC were identified as potential risk factors for mortality, irrespective of prior ICI use.</div></div>","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"471 ","pages":"Article 123440"},"PeriodicalIF":3.6000,"publicationDate":"2025-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Neurological Sciences","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022510X25000577","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background
While numerous studies have investigated the onset features of myasthenia gravis (MG) complicated with myocarditis, there are few articles focusing on the prognosis of patients with both diseases. This study aims to examine mortality in patients with MG who also have myocarditis, and to summarize the clinical characteristics of deceased patients with both conditions.
Results
A total of 91 patients with MG were included in our study, of which 19 (20.9 %) were diagnosed with myocarditis. Shorter MG duration, thymoma, history of myasthenia crisis (MC) and use of immune checkpoint inhibitors (ICIs) were risk factors for developing myocarditis in MG patients. Among the 13 myocarditis-MG patients who did not receive ICIs, 11(84.6 %) had thymoma and 5 (71.4 %) of the 7 tested were positive for titin-IgG. In all myocarditis-MG patients, 11 (57.9 %) died from myocarditis (average age 51 ± 18 years), with 9 (81.8 %) having thymoma and 5 (45 %) having a history of myasthenia crisis. Compared to the mortality rates of MC patients (16.1 %) and the general MG patients (1.8 %), the mortality rate of myocarditis-MG patients is significantly higher.
Conclusions
The study highlights that MG patients with myocarditis face a significantly increased risk of mortality. Thymoma and a history of MC were identified as potential risk factors for mortality, irrespective of prior ICI use.
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.