Tsai Nai-Wen, Chien Li-Nien, Hung Connie, Kuo Amanda, Chiu Yu-Ting, Lin Hung-Wei, Jian Li-Shan, Chou Kai-Pei, Yeh Jiann-Horng
Department of Neurology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Neurol Ther. 2024 Jun;13(3):809-824. doi: 10.1007/s40120-024-00619-4. Epub 2024 Apr 27.
Myasthenia gravis (MG) is a chronic neuromuscular disease leading to significant disease burden. This study aimed to investigate the epidemiology of MG in Taiwan.
A retrospective study was conducted using the Taiwan National Health Insurance Research Database. Prevalent patients with MG diagnosis (either ocular or generalized MG) from 2013 to 2019 were identified, and 2813 patients with initial MG diagnosis from 2014 to 2019 were further defined as the incident cohort. Patient characteristics, treatment patterns, and the occurrence of MG-related events were analyzed.
The number of prevalent patients with MG increased from 4476 in 2013 to 5752 in 2019, with the prevalence rate increasing from 19 to 24 per 100,000 population. The incidence rate also slightly increased from 1.9 to 2.3 per 100,000 population during the study period. Almost all incident patients (99%, n = 2791) received MG-related treatment during the follow-up period. Among 1876 patients who received monotherapy as their initial treatment in the outpatient setting, the mean time from the index date to initial treatment was 48.8 (standard deviation 164.3) days, and most patients received acetylcholinesterase inhibitors (88.5%, n = 1661) as their initial treatment. During the first year after the index date, 133 (4.7%) incident patients experienced their first myasthenic crisis, and 96.2% of these events occurred within 3 months.
The prevalence of MG increased steadily in Taiwan, and the treatment of patients with MG was consistent with guidelines. Despite a high treatment rate, patients still experienced MG-related events, highlighting the limitation of current treatments and emphasizing the need for early intervention and novel treatment approaches.
重症肌无力(MG)是一种慢性神经肌肉疾病,会导致严重的疾病负担。本研究旨在调查台湾地区重症肌无力的流行病学情况。
利用台湾全民健康保险研究数据库进行回顾性研究。确定2013年至2019年期间诊断为重症肌无力(无论是眼肌型还是全身型重症肌无力)的现患患者,并将2014年至2019年首次诊断为重症肌无力的2813例患者进一步定义为发病队列。分析患者特征、治疗模式以及重症肌无力相关事件的发生情况。
重症肌无力现患患者数量从2013年的4476例增加到2019年的5752例,患病率从每10万人19例增加到24例。在研究期间,发病率也从每10万人1.9例略有增加至2.3例。几乎所有发病患者(99%,n = 2791)在随访期间都接受了重症肌无力相关治疗。在1876例门诊初始治疗采用单一疗法的患者中,从索引日期到初始治疗的平均时间为48.8天(标准差164.3),大多数患者初始治疗采用乙酰胆碱酯酶抑制剂(88.5%,n = 1661)。在索引日期后的第一年,133例(4.7%)发病患者经历了首次重症肌无力危象,其中96.2%的事件发生在3个月内。
台湾地区重症肌无力的患病率稳步上升,对重症肌无力患者的治疗符合指南。尽管治疗率较高,但患者仍会发生重症肌无力相关事件,凸显了当前治疗的局限性,并强调了早期干预和新治疗方法的必要性。