Mellen Center for Multiple Sclerosis, Department of Neurology, Cleveland Clinic, Cleveland, OH, USA.
Brigham Multiple Sclerosis Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
J Neurol. 2024 Apr;271(4):1497-1514. doi: 10.1007/s00415-023-12021-5. Epub 2023 Oct 21.
Early treatment initiation in multiple sclerosis (MS) is crucial in preventing irreversible neurological damage and disability progression. The current assessment of disease activity relies on relapse rates and magnetic resonance imaging (MRI) lesion activity, but inclusion of other early, often "hidden," indicators of disease activity may describe a more comprehensive picture of MS.
Early indicators of MS disease activity other than relapses and MRI activity, such as cognitive impairment, brain atrophy, and fatigue, are not typically captured by routine disease monitoring. Furthermore, silent progression (neurological decline not clearly captured by standard methods) may occur undetected by relapse and MRI lesion activity monitoring. Consequently, patients considered to have no disease activity actually may have worsening disease, suggesting a need to revise MS management strategies with respect to timely initiation and escalation of disease-modifying therapy (DMT). Traditionally, first-line MS treatment starts with low- or moderate-efficacy therapies, before escalating to high-efficacy therapies (HETs) after evidence of breakthrough disease activity. However, multiple observational studies have shown that early initiation of HETs can prevent or reduce disability progression. Ongoing randomized clinical trials are comparing escalation and early HET approaches.
There is an urgent need to reassess how MS disease activity and worsening are measured. A greater awareness of "hidden" indicators, potentially combined with biomarkers to reveal silent disease activity and neurodegeneration underlying MS, would provide a more complete picture of MS and allow for timely therapeutic intervention with HET or switching DMTs to address suboptimal treatment responses.
多发性硬化症(MS)的早期治疗启动对于预防不可逆的神经损伤和残疾进展至关重要。目前,疾病活动的评估依赖于复发率和磁共振成像(MRI)病变活动,但纳入其他早期、通常是“隐匿”的疾病活动指标可能会更全面地描述 MS。
除了复发和 MRI 活动外,MS 疾病活动的其他早期指标,如认知障碍、脑萎缩和疲劳,通常不会被常规疾病监测所捕捉。此外,沉默进展(标准方法无法明确捕捉到的神经功能下降)可能在复发和 MRI 病变活动监测中未被发现。因此,被认为没有疾病活动的患者实际上可能病情在恶化,这表明需要修订 MS 管理策略,以便及时启动和升级疾病修正治疗(DMT)。传统上,一线 MS 治疗从低或中效疗法开始,在出现突破性疾病活动后升级为高效疗法(HET)。然而,多项观察性研究表明,早期使用 HET 可以预防或减少残疾进展。正在进行的随机临床试验正在比较升级和早期 HET 方法。
迫切需要重新评估如何衡量 MS 疾病活动和恶化。更深入地了解“隐匿”指标,可能结合生物标志物来揭示 MS 背后的隐匿性疾病活动和神经退行性变,将提供更全面的 MS 情况,并允许及时进行 HET 治疗干预或切换 DMT 以解决治疗反应不佳的问题。