Baakman Anne Catrien, Gavan Carmen, van Doeselaar Lotte, de Kam Marieke, Broekhuizen Karen, Bajenaru Ovidiu, Camps Laura, Swart Eleonora L, Kalisvaart Kees, Schoonenboom Niki, Lemstra Evelien, Scheltens Philip, Cohen Adam, van Gerven Joop, Groeneveld Geert Jan
Centre for Human Drug Research, Leiden, The Netherlands.
Clinicii de neurologie a Spitalului Universitar de Urgenta, Bucharest, Romania.
Br J Clin Pharmacol. 2022 Jun;88(6):2814-2829. doi: 10.1111/bcp.15206. Epub 2022 Jan 26.
Cholinesterase inhibitors (CEIs) have been shown to improve cognitive functioning in Alzheimer's disease (AD) patients, but are associated with multiple side effects and only 20-40% of the patients clinically improve. In this study, we aimed to investigate the acute pharmacodynamic (PD) effects of administration of a single dose of galantamine on central nervous system (CNS) functioning in mild to moderate AD patients and its potential to predict long-term treatment response.
This study consisted of a challenge and treatment phase. In the challenge phase, a single dose of 16 mg galantamine was administered to 50 mild to moderate AD patients in a double-blind, placebo-controlled cross-over fashion. Acute PD effects were monitored up to 5 hours after administration with use of the NeuroCart CNS test battery and safety and pharmacokinetics were assessed. In the treatment phase, patients were treated with open-label galantamine according to regular clinical care. After 6 months of galantamine treatment, patients were categorized as either responder or as non-responder based on their minimental state examination (MMSE), neuropsychiatric inventory (NPI) and disability assessment in dementia (DAD) scores. An analysis of covariance was performed to study the difference in acute PD effects during the challenge phase between responders and non-responders.
A single dose of galantamine significantly reduced saccadic reaction time (-0.0099; 95% CI = -0.0195, -0.0003; P = .0430), absolute frontal EEG parameters in alpha (-14.9; 95% CI = -21.0, -8.3; P = .0002), beta (-12.6; 95% CI = -19.4, -5.3; P = .0019) and theta (-17.9; 95% CI = -25.0, -10.0; P = .0001) frequencies. Relative frontal (-1.669; 95% CI = -2.999, -0.339; P = .0156) and occipital (-1.856; 95% CI = -3.339, -0.372; P = .0166) EEG power in theta frequency and relative occipital EEG power in the gamma frequency (1.316; 95% CI = 0.158, 2.475; P = .0273) also increased significantly compared to placebo. Acute decreases of absolute frontal alpha (-20.4; 95% CI = -31.6, -7.47; P = .0046), beta (-15.7; 95% CI = -28.3, -0.93; P = .0390) and theta (-25.9; 95% CI = -38.4, -10.9; P = .0024) EEG parameters and of relative frontal theta power (-3.27%; 95% CI = -5.96, -0.58; P = .0187) on EEG significantly distinguished responders (n = 11) from non-responders (n = 32) after 6 months.
This study demonstrates that acute PD effects after single dose of galantamine are correlated with long-term treatment effects and that patients who demonstrate a reduction in EEG power in the alpha and theta frequency after a single administration of galantamine 16 mg will most likely respond to treatment.
胆碱酯酶抑制剂(CEIs)已被证明可改善阿尔茨海默病(AD)患者的认知功能,但与多种副作用相关,且仅有20%-40%的患者在临床上有所改善。在本研究中,我们旨在调查单剂量加兰他敏给药对轻度至中度AD患者中枢神经系统(CNS)功能的急性药效学(PD)效应及其预测长期治疗反应的潜力。
本研究包括一个激发试验阶段和一个治疗阶段。在激发试验阶段,以双盲、安慰剂对照交叉方式给50例轻度至中度AD患者单次服用16毫克加兰他敏。给药后长达5小时使用NeuroCart中枢神经系统测试组合监测急性PD效应,并评估安全性和药代动力学。在治疗阶段,根据常规临床护理,患者接受开放标签的加兰他敏治疗。加兰他敏治疗6个月后,根据患者的简易精神状态检查表(MMSE)、神经精神科问卷(NPI)和痴呆症残疾评估(DAD)评分将患者分为反应者或无反应者。进行协方差分析以研究反应者和无反应者在激发试验阶段急性PD效应的差异。
单剂量加兰他敏显著缩短了扫视反应时间(-0.0099;95%置信区间=-0.0195,-0.0003;P=0.0430),显著降低了α(-14.9;95%置信区间=-21.0,-8.3;P=0.0002)、β(-12.6;95%置信区间=-19.4,-5.3;P=0.0019)和θ(-17.9;95%置信区间=-25.0,-10.0;P=0.0001)频率下的绝对额叶脑电图参数。与安慰剂相比,θ频率下的相对额叶(-1.669;95%置信区间=-2.999,-0.339;P=0.0156)和枕叶(-1.856;95%置信区间=-3.339,-0.372;P=0.0166)脑电图功率以及γ频率下的相对枕叶脑电图功率(1.316;95%置信区间=0.158,2.475;P=0.0273)也显著增加。6个月后,绝对额叶α(-20.4;95%置信区间=-31.6,-7.47;P=0.0046)、β(-15.7;95%置信区间=-28.3,-0.93;P=0.0390)和θ(-25.9;95%置信区间=-38.4,-10.9;P=0.0024)脑电图参数以及脑电图上相对额叶θ功率(-3.27%;95%置信区间=-5.96,-0.58;P=0.0187)的急性降低显著区分了反应者(n=11)和无反应者(n=32)。
本研究表明,单剂量加兰他敏后的急性PD效应与长期治疗效果相关,单次服用16毫克加兰他敏后α和θ频率脑电图功率降低的患者很可能对治疗有反应。