Buscarinu Maria Chiara, Reniè Roberta, Morena Emanuele, Romano Carmela, Bellucci Gianmarco, Marrone Antonio, Bigi Rachele, Salvetti Marco, Ristori Giovanni
Department of Neuroscience, Mental Health, and Sensory Organs, Sapienza University, Rome, Italy.
Neuroimmunology Unit, IRCCS Fondazione Santa Lucia, Rome, Italy.
Front Neurol. 2022 Mar 10;13:829331. doi: 10.3389/fneur.2022.829331. eCollection 2022.
Multiple sclerosis (MS), an inflammatory demyelinating and neurodegenerative disease of the central nervous system, usually begins between the ages of 20 and 49 years, though in rare cases it is diagnosed in childhood and adolescence before the age of 18 years, or at the age of 50 years and later. When the onset of the disease occurs at 50 years or older it is conventionally defined as late onset MS (LOMS). Compared to classical MS, the LOMS is characterized by progressive course, a greater delay in diagnosis and a higher prevalence of motor disability. The older the patients, the greater is the risk of comorbidities that can negatively influence the course of the disease and can limit therapeutic strategies. To date, there is no study focused on the efficacy of Disease Modifying Therapies (DMT) in older patients with MS. The only data available are retrievable from subgroup analysis from phase-3 trials of DMT efficacy. In this work, we discuss how the aging process influences the onset, the clinical course and the therapeutic approach in LOMS.
多发性硬化症(MS)是一种中枢神经系统的炎性脱髓鞘和神经退行性疾病,通常发病于20至49岁之间,不过在极少数情况下,它也会在18岁之前的儿童期和青少年期被诊断出来,或者在50岁及以后发病。当疾病在50岁及以上发病时,传统上被定义为晚发性多发性硬化症(LOMS)。与经典型MS相比,LOMS的特点是病程呈进行性、诊断延迟时间更长以及运动功能障碍的患病率更高。患者年龄越大,出现合并症的风险就越高,这些合并症会对疾病进程产生负面影响,并可能限制治疗策略。迄今为止,尚无针对老年MS患者疾病修正治疗(DMT)疗效的研究。现有的唯一数据可从DMT疗效的3期试验亚组分析中获取。在这项工作中,我们讨论了衰老过程如何影响LOMS的发病、临床病程和治疗方法。