Di Stefano Vincenzo, Iacono Salvatore, Militello Massimiliano, Leone Olga, Rispoli Marianna Gabriella, Ferri Laura, Ajdinaj Paola, Lanza Placido, Lupica Antonino, Crescimanno Grazia, Monastero Roberto, Di Muzio Antonio, Brighina Filippo
Department of Biomedicine, Neuroscience, and Advanced Diagnostic (BIND), University of Palermo, Palermo, Italy.
Department of Neuroscience, Imaging and Clinical Sciences, "G. D'Annunzio" University, Chieti, Italy.
Neurol Sci. 2024 Jul;45(7):3481-3494. doi: 10.1007/s10072-024-07368-0. Epub 2024 Feb 22.
Myasthenia gravis (MG) is an autoimmune disorder with fluctuating weakness that causes significant disability and morbidity. Comorbidities may influence the course of MG, particularly in specific subgroups. The aim of this study is to investigate the frequency of comorbidities in MG patients compared to healthy controls (HC) and to evaluate their distribution according to age at disease onset, sex, and disease severity.
MG patients attending the University Hospital "Paolo Giaccone" in Palermo and "SS Annunziata" Hospital in Chieti were enrolled; HC were enrolled from the general population. Non-parametric statistics and logistic regression were used to assess the association of specific comorbidities according to age at disease onset, sex, disease subtypes, and severity of the disease.
A total of 356 subjects were included in the study: 178 MG patients (46% F; median age 60 years [51-71]) and 178 sex- and age-matched HC (46% F, median age 59 years [50-66]). Overall, 86% of MG patients and 76% of HC suffered from comorbidities, and MG patients had a higher number of comorbidities compared to HC. Patients with late-onset suffered from more comorbidities than those with early-onset MG. Hypertension was more common in male patients with MG, while thymic hyperplasia, osteoporosis, and autoimmune diseases were more common in females. Respiratory disorders and thymoma were more common in patients with more severe disease (p < 0.05 for all comparisons).
MG patients, particularly those with late onset, showed a higher prevalence of comorbidities than HC. Assessment of comorbidities in MG is an essential issue to identify the appropriate treatment and achieve the best management.
重症肌无力(MG)是一种自身免疫性疾病,肌无力症状波动,可导致严重的残疾和发病。合并症可能影响重症肌无力的病程,尤其是在特定亚组中。本研究的目的是调查重症肌无力患者与健康对照(HC)相比合并症的发生率,并根据发病年龄、性别和疾病严重程度评估其分布情况。
招募在巴勒莫的“保罗·贾科内”大学医院和基耶蒂的“圣安农齐亚塔”医院就诊的重症肌无力患者;健康对照从普通人群中招募。采用非参数统计和逻辑回归分析,根据发病年龄、性别、疾病亚型和疾病严重程度评估特定合并症的关联性。
本研究共纳入356名受试者:178例重症肌无力患者(女性占46%;中位年龄60岁[51 - 71岁])和178名年龄和性别匹配的健康对照(女性占46%,中位年龄59岁[50 - 66岁])。总体而言,86%的重症肌无力患者和76%的健康对照患有合并症,且重症肌无力患者的合并症数量多于健康对照。晚发型患者的合并症比早发型重症肌无力患者更多。高血压在男性重症肌无力患者中更常见,而胸腺增生、骨质疏松和自身免疫性疾病在女性中更常见。呼吸系统疾病和胸腺瘤在病情较重的患者中更常见(所有比较p < 0.05)。
重症肌无力患者,尤其是晚发型患者,合并症的患病率高于健康对照。评估重症肌无力患者的合并症是确定合适治疗方法并实现最佳管理的关键问题。