Yildiz Ayşegül, Aydin Burç, Gökmen Necati, Yurt Ayşegül, Cohen Bruce, Keskinoglu Pembe, Öngür Dost, Renshaw Perry
Department of Psychiatry, School of Medicine, Dokuz Eylul University, Izmir, Turkey.
Department of Medical Pharmacology, School of Medicine, Dokuz Eylul University, Izmir, Turkey.
Biol Psychiatry Cogn Neurosci Neuroimaging. 2016 Mar;1(2):125-131. doi: 10.1016/j.bpsc.2015.12.002.
The antimanic efficacy of a protein kinase C (PKC) inhibitor, tamoxifen, has been tested in several clinical trials, all reporting positive results. However, mechanisms underlying the observed clinical effects requires further confirmation through studies of biological markers.
We investigated the effect of tamoxifen versus placebo on brain metabolites via a proton (H) magnetic resonance spectroscopy (MRS) study. Forty-eight adult bipolar I manic patients (mean Young Mania Rating Scale (YMRS) score of 37.8±5.8) were scanned at baseline and following 3 weeks of double-blind treatment. We hypothesized that manic symptom alleviation would improve the levels of markers associated with brain energy metabolism (creatine plus phosphocreatine [total creatine; tCr]) and neuronal viability (N-acetylaspartate [NAA]).
The YMRS scores decreased from 38.6±4.5 to 20.0±11.1 in the tamoxifen group and increased from 37.0±6.8 to 43.1±7.8 in the placebo group (p<0.001). H MRS measurements revealed a 5.5±13.8% increase in the dorsomedial prefrontal cortex (DMPFC) tCr levels in the tamoxifen group and a 5.3±13.1% decrease in tCr in the placebo group (p=0.027). A significant correlation between the YMRS score change and tCr percent change was observed in the whole group (Spearman ρ=0.341, p=0.029). Both tCr and NAA levels in the responder group were increased by 9.4±15.2% and 6.1±11.7%, whereas levels in the non-responder group were decreased by 2.1±13.2% and 6.5±10.5%, respectively (p<0.05).
Tamoxifen effectively treated mania while it also increased brain tCr levels, consistent with involvement of both excessive PKC activation and impaired brain energy metabolism in the development of bipolar mania.
Registry name: ClinicalTrials.gov URL: https://clinicaltrials.gov/ct2/show/NCT00411203?term=NCT00411203&rank=1 Registration number: NCT00411203.
蛋白激酶C(PKC)抑制剂他莫昔芬的抗躁狂疗效已在多项临床试验中得到检验,所有试验均报告了阳性结果。然而,观察到的临床效果背后的机制需要通过生物标志物研究进一步证实。
我们通过质子(H)磁共振波谱(MRS)研究调查了他莫昔芬与安慰剂对脑代谢物的影响。48名成年双相I型躁狂患者(平均杨氏躁狂量表(YMRS)评分为37.8±5.8)在基线时以及双盲治疗3周后接受扫描。我们假设躁狂症状的缓解会改善与脑能量代谢相关的标志物(肌酸加磷酸肌酸[总肌酸;tCr])和神经元活力(N-乙酰天门冬氨酸[NAA])的水平。
他莫昔芬组的YMRS评分从38.6±4.5降至20.0±11.1,安慰剂组从37.0±6.8升至43.1±7.8(p<0.001)。H MRS测量显示,他莫昔芬组背内侧前额叶皮质(DMPFC)的tCr水平增加了5.5±13.8%,安慰剂组的tCr水平下降了5.3±13.1%(p=0.027)。在整个组中观察到YMRS评分变化与tCr百分比变化之间存在显著相关性(Spearman ρ=0.341,p=0.029)。应答组的tCr和NAA水平分别增加了9.4±15.2%和6.1±11.7%,而非应答组的水平分别下降了2.1±13.2%和6.5±10.5%(p<0.05)。
他莫昔芬有效治疗躁狂,同时还增加了脑tCr水平,这与双相躁狂症发展过程中PKC过度激活和脑能量代谢受损均有关。
注册名称:ClinicalTrials.gov网址:https://clinicaltrials.gov/ct2/show/NCT00411203?term=NCT00411203&rank=1注册号:NCT00411203