Yildiz Ayşegül, Guleryuz Sebnem, Ankerst Donna Pauler, Ongür Dost, Renshaw Perry F
Department of Psychiatry, Dokuz Eylül University, Huzur Mah, Saffet Baba Sok, No. 27/12 PK: 35320 Narlidere, Izmir, Turkey.
Arch Gen Psychiatry. 2008 Mar;65(3):255-63. doi: 10.1001/archgenpsychiatry.2007.43.
Findings that protein kinase C (PKC) activity may be altered in mania, and that both lithium carbonate and valproate sodium inhibit PKC-associated signaling in brain tissue, encourage development of PKC inhibitors as candidate antimanic agents.
To perform a controlled test of antimanic efficacy of the centrally active PKC inhibitor tamoxifen citrate.
Three-week, randomized, double-blind, placebo-controlled, parallel-arms trial.
A university medical center inpatient psychiatric unit in Izmir, Turkey.
Sixty-six patients aged 18 to 60 years, diagnosed as having DSM-IV bipolar I disorder on the basis of the Structured Clinical Interview for DSM-IV, currently in a manic or mixed state, with or without psychotic features, with initial scores on the Young Mania Rating Scale (YMRS) greater than 20.
Treatment with tamoxifen or identical placebo tablets for up to 3 weeks. Adjunctive lorazepam was allowed up to 5 mg/d.
Primary: change in YMRS scores; secondary: change in Clinical Global Impressions-Mania scores, weekly ratings of depression and psychosis, and adjunctive use of lorazepam.
The 21-day trial was completed by 29 of 35 subjects randomized to receive tamoxifen (83%) and 21 of 31 given placebo (68%) (P = .25). Intent-to-treat analysis of available measures on all 66 subjects indicated that tamoxifen treatment yielded mean decreases in scores on the YMRS and Clinical Global Impressions-Mania of 5.84 and 0.73 point per week, respectively, compared with mean increases of 1.50 and 0.10 point per week, respectively, with placebo; both drug-placebo contrasts differed significantly (P < .001).
Tamoxifen demonstrated antimanic properties and was remarkably well tolerated. The findings encourage further clarification of the role of PKC in the pathophysiologic mechanism of bipolar I disorder and development of novel anti-PKC agents as potential antimanic or mood-stabilizing agents.
clinicaltrials.gov Identifier: NCT00411203 and isrctn.org Identifier: ISRCTN97160532.
有研究发现,躁狂症患者蛋白激酶C(PKC)活性可能发生改变,且碳酸锂和丙戊酸钠均可抑制脑组织中与PKC相关的信号传导,这促使人们研发PKC抑制剂作为候选抗躁狂药物。
对中枢活性PKC抑制剂枸橼酸他莫昔芬的抗躁狂疗效进行对照试验。
为期3周的随机、双盲、安慰剂对照、平行组试验。
土耳其伊兹密尔一所大学医学中心的住院精神科病房。
66例年龄在18至60岁之间的患者,根据《精神疾病诊断与统计手册》第四版(DSM-IV)的结构化临床访谈被诊断为DSM-IV双相I型障碍,目前处于躁狂或混合状态,有或无精神病性症状,杨氏躁狂评定量表(YMRS)初始评分大于20分。
服用他莫昔芬或相同的安慰剂片,最长3周。允许加用劳拉西泮,剂量最高可达5mg/d。
主要指标:YMRS评分的变化;次要指标:临床总体印象-躁狂评分的变化、抑郁和精神病症状的每周评分以及劳拉西泮的加用情况。
随机接受他莫昔芬治疗的35名受试者中有29名(83%)完成了为期21天的试验,服用安慰剂的31名受试者中有21名(68%)完成试验(P = 0.25)。对所有66名受试者的可用测量数据进行意向性分析表明, 与安慰剂组每周平均增加1.50分和0.10分相比,他莫昔芬治疗组的YMRS评分和临床总体印象-躁狂评分每周平均分别降低5.84分和0.73分;两种药物与安慰剂的对比均有显著差异(P < 0.001)。
他莫昔芬具有抗躁狂特性,且耐受性良好。这些研究结果有助于进一步阐明PKC在双相I型障碍病理生理机制中的作用,并推动新型抗PKC药物作为潜在抗躁狂或心境稳定剂的研发。
clinicaltrials.gov标识符:NCT00411203;isrctn.org标识符:ISRCTN97160532。