Suppes Trisha, Marangell Lauren B, Bernstein Ira H, Kelly Dorothy I, Fischer E Grace, Zboyan Holly A, Snow Diane E, Martinez Melissa, Al Jurdi Rayan, Shivakumar Geetha, Sureddi Suresh, Gonzalez Robert
Bipolar Disorders Research Program, Department of Psychiatry, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390-9121, United States.
J Affect Disord. 2008 Dec;111(2-3):334-43. doi: 10.1016/j.jad.2008.02.004. Epub 2008 Mar 20.
Treatment studies are lacking for patients with bipolar II disorder (BDII). The objective of this study was to compare lamotrigine (LTG) and lithium (Li) monotherapy for the treatment of BDII depression.
Patients with BDII acute depression were randomized to open-label monotherapy with LTG or Li, and evaluated by trained raters blinded to treatment. Patients were titrated to 200 mg/day of LTG over 8 weeks or at least 900 mg/day of Li over 2 weeks (serum level 0.6-1.2 mEq/L), and seen biweekly for 16 weeks. The primary outcome variable was change in the Hamilton Depression Rating Scale 17-item (Ham-D(17)), evaluated using mixed effects random regression.
Both groups showed significant improvement from baseline to endpoint on the Ham-D(17) (p<0.0001), with no between group differences (p=0.95). Seventy-two percent of the population was rapid cycling by DSM-IV criteria. No differences in response were noted between rapid cyclers and non-rapid cyclers. Early termination for any cause was 42%. The Li group reported significantly more side effects, although drop-out due to side effects did not differ between groups.
This study was limited by an open treatment design, a lack of placebo arm, and uneven treatment groups.
Lamotrigine and lithium were effective monotherapy for BDII depression, with comparable response and remission rates. Naturalistic design and lack of placebo limit conclusions, though patient history indicated long standing depression unlikely to be alleviated by time. Patients who received Li reported more side effects, but this did not appear to impact drop-out rates.
双相II型障碍(BDII)患者缺乏治疗研究。本研究的目的是比较拉莫三嗪(LTG)和锂盐(Li)单药治疗BDII抑郁的效果。
BDII急性抑郁患者被随机分配接受LTG或Li的开放标签单药治疗,并由对治疗不知情的经过培训的评估者进行评估。患者在8周内滴定至LTG 200mg/天或在2周内滴定至Li至少900mg/天(血清水平0.6 - 1.2mEq/L),每两周就诊一次,共16周。主要结局变量是汉密尔顿抑郁评定量表17项(Ham - D(17))的变化,采用混合效应随机回归进行评估。
两组在Ham - D(17)上从基线到终点均有显著改善(p<0.0001),组间无差异(p = 0.95)。根据《精神疾病诊断与统计手册》第四版(DSM - IV)标准,72%的患者为快速循环型。快速循环型和非快速循环型患者在反应上无差异。因任何原因提前终止治疗的比例为42%。Li组报告的副作用明显更多,尽管因副作用导致的退出率在两组间无差异。
本研究受开放治疗设计、缺乏安慰剂组和治疗组不均衡的限制。
拉莫三嗪和锂盐是治疗BDII抑郁的有效单药,反应率和缓解率相当。自然主义设计和缺乏安慰剂限制了结论,尽管患者病史表明长期抑郁不太可能随时间缓解。接受Li治疗的患者报告的副作用更多,但这似乎并未影响退出率。