Hilz Max J, Wang Ruihao, de Rojas Leal Carmen, Liu Mao, Canavese Francesca, Roy Sankanika, Hösl Katharina M, Winder Klemens, Lee De-Hyung, Linker Ralf A
Clinical Department of Autonomic Neurology, University College London Institute of Neurology, Queen Square, WC1N 3BG, London, UK, Department of Neurology, University of Erlangen-Nuremberg, Erlangen, Germany.
Department of Neurology, University of Erlangen-Nuremberg, Erlangen, Germany.
Ther Adv Neurol Disord. 2017 Apr;10(4):191-209. doi: 10.1177/1756285616682936. Epub 2017 Jan 6.
Fingolimod slows heart rate (HR) due to vagomimetic effects and might cause additional cardiovascular autonomic changes. While the time course of HR changes is well described, the extent and course of cardiovascular autonomic changes upon fingolimod initiation has not yet been evaluated. This study, therefore, intended to assess cardiovascular autonomic changes during the first 6 h after fingolimod initiation.
In 21 patients with relapsing-remitting multiple sclerosis (RRMS), we recorded respiration (RESP), electrocardiographic RR interval (RRI), systolic and diastolic blood pressure (BPsys, BPdia) at rest, before and 0.5, 1, 2, 3, 4, 5, and 6 h after fingolimod initiation. We calculated parameters of total autonomic modulation [RRI standard deviation (RRI-SD), RRI coefficient of variation (RRI-CV), RRI-total powers], mainly sympathetic cardiac modulation [RRI low frequency (LF) powers], sympathetic BP modulation (BPsys-LF powers), parasympathetic modulation [square root of the mean squared difference of successive RRIs (RMSSD), RRI high frequency (HF) powers], sympatho-vagal cardiac balance (RRI-LF/HF ratios), and baroreflex sensitivity (BRS). We compared parameters between the eight measurements [analysis of variance (ANOVA) or Friedman test with analysis; significance: < 0.05].
After fingolimod initiation, RESP, BPsys, and BPsys-LF powers remained unchanged while RRIs, RRI-CV, RRI-SD, RRI-total powers, RRI-LF powers, RMSSD, RRI-HF powers, and BRS increased after 1 h and rose to peak values occurring after 5, 1, 2, 2, 1, 4, 4, and 4 h, respectively. After 3 h, BPdia had decreased significantly and was lowest after 5 h. RRI-LF/HF ratios decreased to a nadir after 4 h.
The increases in parasympathetic and overall cardiac autonomic modulation and in BRS seen with fingolimod initiation are theoretically beneficial for the MS patient's cardiovascular system. However, long-term studies must show whether these effects persist or are attenuated (e.g. due to S1P1 receptor down-regulation upon continued fingolimod therapy).
芬戈莫德因拟迷走神经作用会减慢心率(HR),并可能引起额外的心血管自主神经变化。虽然心率变化的时间进程已有详尽描述,但开始使用芬戈莫德后心血管自主神经变化的程度和进程尚未得到评估。因此,本研究旨在评估开始使用芬戈莫德后最初6小时内的心血管自主神经变化。
在21例复发缓解型多发性硬化症(RRMS)患者中,我们记录了静息状态下、开始使用芬戈莫德前以及用药后0.5、1、2、3、4、5和6小时的呼吸(RESP)、心电图RR间期(RRI)、收缩压和舒张压(BPsys、BPdia)。我们计算了总自主神经调节参数[RRI标准差(RRI-SD)、RRI变异系数(RRI-CV)、RRI总功率]、主要是交感神经心脏调节参数[RRI低频(LF)功率]、交感神经血压调节参数(BPsys-LF功率)、副交感神经调节参数[连续RRIs均方差的平方根(RMSSD)、RRI高频(HF)功率]、交感-迷走神经心脏平衡参数(RRI-LF/HF比值)和压力反射敏感性(BRS)。我们比较了八次测量之间的参数[方差分析(ANOVA)或Friedman检验及分析;显著性:<0.05]。
开始使用芬戈莫德后,RESP、BPsys和BPsys-LF功率保持不变,而RRIs、RRI-CV、RRI-SD、RRI总功率、RRI-LF功率、RMSSD、RRI-HF功率和BRS在1小时后增加,并分别在5、1、2、2、1、4、4和4小时达到峰值。3小时后,BPdia显著下降,并在5小时时最低。RRI-LF/HF比值在4小时后降至最低点。
开始使用芬戈莫德时观察到的副交感神经和整体心脏自主神经调节以及BRS的增加在理论上对MS患者的心血管系统有益。然而,长期研究必须表明这些效应是否持续存在或减弱(例如由于持续使用芬戈莫德治疗导致S1P1受体下调)。