Vieta Eduard, Suppes Trisha, Eggens Ivan, Persson Inger, Paulsson Björn, Brecher Martin
Clinical Institute of Neuroscience, Hospital Clinic, University of Barcelona, IDIBAPS, CIBER-SAM, Barcelona, Spain.
J Affect Disord. 2008 Aug;109(3):251-63. doi: 10.1016/j.jad.2008.06.001. Epub 2008 Jun 24.
This study examined the efficacy and safety of quetiapine in combination with lithium or divalproex compared with placebo with lithium or divalproex in the prevention of recurrent mood events in bipolar I patients, most recent episode mania, depression, or mixed.
Patients received open-label quetiapine (400-800 mg/day; flexible, divided doses) with lithium or divalproex (target serum concentrations 0.5-1.2 mEq/L and 50-125 microg/mL, respectively) for up to 36 weeks to achieve at least 12 weeks of clinical stability. Patients were subsequently randomized to double-blind treatment with quetiapine (400-800 mg/day) plus lithium/divalproex or placebo plus lithium/divalproex for up to 104 weeks. The primary endpoint was time to recurrence of any mood event.
Treatment with quetiapine in combination with lithium/divalproex significantly increased the time to recurrence of any mood event compared with placebo plus lithium/divalproex. The proportion of patients having a mood event was markedly lower in the quetiapine than in the placebo group (18.5% versus 49.0%). The hazard ratio for time to recurrence of a mood event was 0.28 (P<0.001), a mania event 0.30 (P<0.001), and a depression event 0.26 (P<0.001) corresponding to risk reductions of 72%, 70%, and 74%, respectively. During the randomization phase, the most common adverse events occurring in > or =5% in the quetiapine group were somnolence, nasopharyngitis, and headache. Insomnia was more common in the placebo group. During the randomization phase, there was an increase in weight of 0.5 kg in the quetiapine group and a reduction of 1.9 kg in the placebo group. The incidence and incidence density of a single emergent fasting blood glucose value> or =126 mg/dL was higher with quetiapine than with placebo (9.3% versus 4.1%; 17.6 versus 9.5 patients per 100 patient-years).
This was an enriched sample of patients with bipolar I disorder responding to treatment with quetiapine plus lithium/divalproex.
Maintenance treatment with quetiapine in combination with lithium/divalproex significantly increased time to recurrence of any event (mania, depression, or mixed) irrespective of the polarity of the index episode compared with placebo with lithium/divalproex. Long-term treatment with quetiapine was generally well-tolerated. Quetiapine with lithium/divalproex can provide an effective long-term treatment option for bipolar I disorder to prevent recurrences not only of mania but also depression.
本研究比较了喹硫平联合锂盐或丙戊酸与安慰剂联合锂盐或丙戊酸在预防I型双相情感障碍患者(最近一次发作是躁狂、抑郁或混合发作)复发情绪事件方面的疗效和安全性。
患者接受开放标签的喹硫平(400 - 800毫克/天;灵活分剂量)联合锂盐或丙戊酸(目标血清浓度分别为0.5 - 1.2毫当量/升和50 - 125微克/毫升)治疗长达36周,以实现至少12周的临床稳定。随后患者被随机分配接受双盲治疗,使用喹硫平(400 - 800毫克/天)加锂盐/丙戊酸或安慰剂加锂盐/丙戊酸,治疗长达104周。主要终点是任何情绪事件复发的时间。
与安慰剂加锂盐/丙戊酸相比,喹硫平联合锂盐/丙戊酸治疗显著延长了任何情绪事件复发的时间。喹硫平组发生情绪事件的患者比例明显低于安慰剂组(18.5%对49.0%)。情绪事件复发时间的风险比为0.28(P<0.001),躁狂事件为0.30(P<0.001),抑郁事件为0.26(P<0.001),分别对应风险降低72%、70%和74%。在随机化阶段,喹硫平组中发生率≥5%的最常见不良事件是嗜睡、鼻咽炎和头痛。失眠在安慰剂组更常见。在随机化阶段,喹硫平组体重增加0.5千克,安慰剂组体重减轻1.9千克。喹硫平组单次空腹血糖值≥126毫克/分升的发生率和发病密度高于安慰剂组(9.3%对4.1%;每100患者年分别为17.6例和9.5例)。
这是一组对喹硫平加锂盐/丙戊酸治疗有反应的I型双相情感障碍患者的富集样本。
与安慰剂联合锂盐/丙戊酸相比,喹硫平联合锂盐/丙戊酸维持治疗显著延长了任何事件(躁狂、抑郁或混合发作)复发的时间,无论索引发作的极性如何。喹硫平长期治疗一般耐受性良好。喹硫平联合锂盐/丙戊酸可为I型双相情感障碍提供一种有效的长期治疗选择,不仅可预防躁狂复发,还可预防抑郁复发。