Zhou Tiantian, Wang Jindong, Xin Cuiyu, Kong Lingli, Wang Chunxia
Department of Geriatric Psychiatry, Qingdao Mental Health Center, Qingdao, Shandong 266034, P.R. China.
Exp Ther Med. 2019 Mar;17(3):1625-1630. doi: 10.3892/etm.2018.7124. Epub 2018 Dec 21.
Among Alzheimer's disease (AD) patients, it is very common to develop behavioral and psychological symptoms of dementia (BPSD), which has a close relation to the excess morbidity and mortality, greater healthcare use, earlier institutionalization, and caregiver burden. With evaluation of AD patients, the present study mainly aims to investigate whether citalopram would be efficient for BPSD, and examines citalopram's effects on cognitive function, caregiver distress, safety and tolerability. Eighty patients diagnosed with moderate AD and clinically significant BPSD from April 2015 to January 2016 were enrolled in this study. Patients randomly received memantine plus either citalopram (n=40, study group) or placebo (n=40, control group) in a 12-week period. The target dose of memantine was 20 mg/day. The dose of citalopram was 10 mg/day in the beginning with planned titration to 30 mg/day over 2 weeks on the basis of response and tolerability. Blood routine, urine routine, biochemical tests, electrocardiogram and electroencephalogram were carried out for each patient every month routinely to check the change induced by using medication. Treatment Emergent Symptom Scale (TESS) was used to measure untoward effects every 2 weeks. All of the agitation/aggression, irritability/lability, night-time behavioral disturbances, caregiver distress and Neuropsychiatric Inventory (NPI) total scores after treatment were found to be dramatically lower than those before treatment in both groups. Apathy, dysphoria and anxiety received lower scores in participants who received memantine combined with citalopram, compared to those before treatment. QTc interval prolongation was observed in 2 patients who were treated with 30 mg/day citalopramin. In conclusion, memantine combined with citalopram can more effectively improve the cognitive function, and reduce behavioral and psychological symptoms in patients with moderate AD. Cardiac adverse effects of citalopram are not common when the dose is <30 mg/day, which does not limit its practical application. Thus, citalopram has shown potential efficacy in adjunctive therapy of AD patients with BPSD.
在阿尔茨海默病(AD)患者中,出现痴呆的行为和心理症状(BPSD)非常常见,这与发病率和死亡率过高、医疗保健使用增加、更早入住养老院以及照料者负担加重密切相关。通过对AD患者的评估,本研究主要旨在调查西酞普兰对BPSD是否有效,并研究西酞普兰对认知功能、照料者痛苦、安全性和耐受性的影响。2015年4月至2016年1月期间,80名被诊断为中度AD且有临床显著BPSD的患者被纳入本研究。患者在12周内随机接受美金刚加西酞普兰(n = 40,研究组)或安慰剂(n = 40,对照组)治疗。美金刚的目标剂量为20毫克/天。西酞普兰的起始剂量为10毫克/天,并根据反应和耐受性计划在2周内滴定至30毫克/天。每月定期对每位患者进行血常规、尿常规、生化检查、心电图和脑电图检查,以检查用药引起的变化。每2周使用治疗中出现的症状量表(TESS)来测量不良反应。结果发现,两组治疗后的所有激越/攻击行为、易激惹/情绪不稳定、夜间行为障碍、照料者痛苦和神经精神科问卷(NPI)总分均显著低于治疗前。与治疗前相比接受美金刚联合西酞普兰治疗的参与者在情感淡漠、烦躁不安和焦虑方面得分较低。2名接受30毫克/天西酞普兰治疗的患者出现QTc间期延长。总之,美金刚联合西酞普兰能更有效地改善中度AD患者的认知功能,并减轻其行为和心理症状。当剂量<30毫克/天时,西酞普兰的心脏不良反应并不常见,这并不限制其实际应用。因此,西酞普兰在AD合并BPSD患者的辅助治疗中显示出潜在疗效。