Moura João, Fernandes Joana, Lima Maria João, Sousa Ana Paula, Samões Raquel, Martins Silva Ana, Santos Ernestina
Department of Neurology, Centro Hospitalar Universitário de Santo António, Porto, Portugal.
Unit of Multidisciplinary Research in Biomedicine (UMIB), Instituto de Ciências Biomédicas Abel Salazar (ICBAS), University of Porto, Porto, Portugal.
Front Neurol. 2024 Mar 11;15:1277420. doi: 10.3389/fneur.2024.1277420. eCollection 2024.
Early-onset (EOMG) and late-onset (LOMG) are distinct groups of MG patients. It is unclear if treatment strategies and treatment-related adverse events may differ according to the age of MG onset.
This single-center retrospective study includes all MG patients followed at a tertiary center since 2007. We reviewed the electronic clinical records.
In total, 212 patients were identified, 142 (67.0%) females, with a median disease duration of 10 years. The median age of symptom onset was 42.0 (26.0-64.5) years, with 130 (61.3%) EOMG cases and 82 (38.7%) LOMG. EOMG were more frequently female, had longer disease duration and often more generalized MG ( < 0.001). Comorbidities were significantly more frequent in LOMG (67.1%) compared to EOMG (53.1%) ( = 0.002). Steroid-related adverse effects motivating the switch to steroid-sparing agents (82.0%) were different between groups, with hypertension, hypercholesterolemia, diabetes mellitus and malignancies being more common in LOMG. At the same time, osteoporosis and dyspepsia were more frequent in EOMG ( < 0.001). The most common first-line choice was azathioprine (45.8%), and rituximab was used in 4 patients (1.9%).
Our study shows that treatment modalities are similar between EOMG and LOMG, while steroid-related adverse events appear to be distinct.
早发型重症肌无力(EOMG)和晚发型重症肌无力(LOMG)是重症肌无力患者的不同群体。目前尚不清楚治疗策略和与治疗相关的不良事件是否会因重症肌无力发病年龄的不同而有所差异。
这项单中心回顾性研究纳入了自2007年以来在一家三级中心随访的所有重症肌无力患者。我们查阅了电子临床记录。
总共确定了212例患者,其中142例(67.0%)为女性,疾病持续时间中位数为10年。症状出现的中位年龄为42.0(26.0 - 64.5)岁,其中130例(61.3%)为早发型重症肌无力病例,82例(38.7%)为晚发型重症肌无力。早发型重症肌无力女性更为常见,疾病持续时间更长,且通常更多为全身性重症肌无力(P < 0.001)。与早发型重症肌无力(53.1%)相比,晚发型重症肌无力(67.1%)的合并症明显更为常见(P = 0.002)。两组之间促使改用类固醇替代药物的类固醇相关不良反应(82.0%)有所不同,高血压、高胆固醇血症、糖尿病和恶性肿瘤在晚发型重症肌无力中更为常见。同时,骨质疏松和消化不良在早发型重症肌无力中更为常见(P < 0.001)。最常见的一线选择是硫唑嘌呤(45.8%),4例患者(1.9%)使用了利妥昔单抗。
我们的研究表明,早发型重症肌无力和晚发型重症肌无力的治疗方式相似,而类固醇相关的不良事件似乎有所不同。