Dietrich D E, Bode L, Spannhuth C W, Lau T, Huber T J, Brodhun B, Ludwig H, Emrich H M
Department of Clinical Psychiatry and Psychotherapy, Medical School Hannover, Germany.
Bipolar Disord. 2000 Mar;2(1):65-70. doi: 10.1034/j.1399-5618.2000.020110.x.
Originally introduced into pharmacotherapy as an antiviral compound, amantadine was shown to also have multiple pharmacological eftfects on the central nervous system. In addition. only a few studies reported on certain antidepressive properties of amantadine. This effect was highlighted by the discovery of its antiviral effect on Borna disease virus (BDV), which is hypothesized to be an etiopathogenetic factor to subtypes of affective disorders. Therefore, the therapeutical use of amantadine in BDV-infected depressive patients was investigated.
In this open trial, amantadine was added to antidepressive and or mood-stabilizing compounds treating BDV-infected depressed patients (n = 25) with bipolar or major depressive disorders. Amantadine was given twice a day (100-300 mg/day) for a mean of 11 weeks. Antidepressive treatment response was measured on the Hamilton rating scale for depression (HAM-D) and/or with an operationalized diagnostic criteria system (OPCRIT: version 3.31). Virological response was measured by expression of BDV infection parameters in blood samples.
The overall response rate of the amantadine augmentation in the BDV-infected patients with regard to depressive symptoms was 68% after a mean of 2.9 weeks of treatment. Bipolar I patients improved faster and did not show any following hypomania. In addition, the decrease of depression tended to correspond with the decrease in viral activity.
Amantadine appears to show a remarkable antidepressive efficacy in BDV-infected depressive patients. The antidepressive effect in this open trial appeared to be comparable to standard antidepressives, possibly being a result of its antiviral effect against BDV as a potentially relevant etiopathogenetic factor in these disorders.
金刚烷胺最初作为一种抗病毒化合物被引入药物治疗,后来发现它对中枢神经系统也有多种药理作用。此外,仅有少数研究报道了金刚烷胺的某些抗抑郁特性。其对博尔纳病病毒(BDV)的抗病毒作用的发现突出了这种效应,据推测BDV是情感障碍亚型的一个病因学因素。因此,对金刚烷胺在BDV感染的抑郁症患者中的治疗应用进行了研究。
在这项开放性试验中,将金刚烷胺添加到治疗BDV感染的双相或重度抑郁症患者(n = 25)的抗抑郁和/或心境稳定剂中。金刚烷胺每日服用两次(100 - 300毫克/天),平均服用11周。通过汉密尔顿抑郁评定量表(HAM - D)和/或操作性诊断标准系统(OPCRIT:版本3.31)来测量抗抑郁治疗反应。通过血液样本中BDV感染参数的表达来测量病毒学反应。
在平均治疗2.9周后,BDV感染患者中金刚烷胺增效治疗在抑郁症状方面的总体有效率为68%。双相I型患者改善更快,且未出现随后的轻躁狂发作。此外,抑郁程度的减轻往往与病毒活性的降低相对应。
金刚烷胺在BDV感染的抑郁症患者中似乎显示出显著的抗抑郁疗效。在这项开放性试验中的抗抑郁效果似乎与标准抗抑郁药相当,这可能是其对BDV的抗病毒作用的结果,BDV可能是这些疾病中一个潜在相关的病因学因素。