Riepl Ester, Pfeuffer Steffen, Ruck Tobias, Lohmann Hubertus, Wiendl Heinz, Meuth Sven G, Johnen Andreas
Department of Neurology, University Hospital Muenster, Muenster, Germany.
Front Neurol. 2018 Jan 16;8:730. doi: 10.3389/fneur.2017.00730. eCollection 2017.
Several disease-modifying drugs have shown promising effects on cognitive impairment in multiple sclerosis (MS). Alemtuzumab, a humanized monoclonal antibody, is effective in controlling disease activity, however, has not been evaluated for its effects on cognition in detail so far.
To explore the influence of alemtuzumab on cognitive impairment in active relapsing-remitting MS (RRMS) as well as possible clinical and neuroimaging predictors of cognitive changes during the first year of therapy.
Extensive neuropsychological assessment was administered to 21 patients with active RRMS at baseline and again after the second treatment with alemtuzumab (mean time span: 15.05 months). Clinical and routine structural neuroimaging markers were explored for their capacity to predict individual courses of cognitive change.
Overall cognitive functioning remained stable or improved during the observational period of alemtuzumab treatment on average. Scores on two neuropsychological tests of processing speed significantly improved and clinically relevant individual gains of processing speed were seen in the majority of patients. Linear regression models showed that clinical and routine neuroimaging measures of disease activity could not fully account for these cognitive changes.
Results suggest that alemtuzumab treatment in active RRMS stabilizes overall cognitive functioning and furthermore positively affects cognitive processing speed. Changes in processing speed were independent from clinical and structural neuroimaging parameters of disease activity and may thus represent an underrated and independent outcome measure to evaluate treatment effects.
几种疾病修饰药物已显示出对多发性硬化症(MS)认知障碍有显著疗效。阿仑单抗,一种人源化单克隆抗体,在控制疾病活动方面有效,然而,迄今为止尚未对其对认知的影响进行详细评估。
探讨阿仑单抗对活动性复发缓解型MS(RRMS)认知障碍的影响,以及治疗第一年期间认知变化的可能临床和神经影像学预测指标。
对21例活动性RRMS患者在基线时以及第二次接受阿仑单抗治疗后(平均时间跨度:15.05个月)进行了广泛的神经心理学评估。探讨临床和常规结构神经影像学标志物预测个体认知变化过程的能力。
在阿仑单抗治疗的观察期内,总体认知功能平均保持稳定或有所改善。两项处理速度神经心理学测试的分数显著提高,大多数患者在临床上有与处理速度相关的个体改善。线性回归模型显示,疾病活动的临床和常规神经影像学测量不能完全解释这些认知变化。
结果表明,阿仑单抗治疗活动性RRMS可稳定总体认知功能,并且进一步对认知处理速度产生积极影响。处理速度的变化独立于疾病活动的临床和结构神经影像学参数,因此可能是评估治疗效果的一个被低估的独立结果指标。