Tom T, Cummings J L
Department of Neurology, UCLA School of Medicine, USA.
Drugs Aging. 1998 Jan;12(1):55-74. doi: 10.2165/00002512-199812010-00006.
Parkinson's disease (PD) is a common neurological illness and various degrees of depression frequently complicate its course. Risk factors for developing depression with PD include right-sided hemiparkinsonism, akinesia, increased severity of disability, anxiety and psychosis. Onset of parkinsonism at a younger age, female gender and the use of levodopa are arguable risk factors. Depression may be difficult to diagnose in patients with PD because the signs of the 2 disorders overlap. In addition, patients with atypical PD more commonly have depression than patients with classical PD presentations. Antidepressant response to antiparkinsonian treatment has been limited. Enhancement of catecholamine levels in the CNS by selegiline (deprenyl), a monoamine oxidase (MAO) type B inhibitor, has shown potential antidepressant as well as neuroprotective effects. Other MAO inhibitors have shown antidepressant efficacy in animal models but have not been well tolerated by patients with PD. A catechol-O-methyltransferase (COMT) inhibitor combined with an MAO inhibitor might synergistically maximise the levels of catecholamines in the CNS. Antidepressant medications used in patients without PD include tricyclic antidepressants (TCAs) and selective serotonin (5-hydroxytryptamine; 5-HT) reuptake inhibitors (SSRIs), but only TCAs have been carefully studied for their antidepressant effects in PD. Electroconvulsive therapy has proven efficacy as antidepressant therapy in patients with PD, and transcranial magnetic stimulation has provided temporary relief of depression under experimental conditions. Adverse effects of polypharmacy in the attempted treatment of depression in patients with PD are common in the elderly. A 'serotonin syndrome' has occurred frequently enough to preclude the coadministration of selegiline with SSRIs or TCAs, and multiple interactions between antiparkinsonian and antidepressant medications further complicate treatment strategies in patients with PD. An algorithmic approach to the pharmacological treatment of depression is described in this article.
帕金森病(PD)是一种常见的神经系统疾病,不同程度的抑郁常常使其病情复杂化。PD患者发生抑郁的危险因素包括右侧偏侧帕金森综合征、运动不能、残疾严重程度增加、焦虑和精神病。较年轻的帕金森病起病、女性以及左旋多巴的使用是否为危险因素尚有争议。PD患者的抑郁可能难以诊断,因为这两种疾病的症状相互重叠。此外,非典型PD患者比典型PD表现的患者更常出现抑郁。抗帕金森病治疗对抑郁的反应有限。单胺氧化酶(MAO)B型抑制剂司来吉兰(丙炔苯丙胺)可提高中枢神经系统(CNS)中儿茶酚胺水平,已显示出潜在的抗抑郁及神经保护作用。其他MAO抑制剂在动物模型中已显示出抗抑郁疗效,但PD患者耐受性不佳。儿茶酚-O-甲基转移酶(COMT)抑制剂与MAO抑制剂联合使用可能协同最大化CNS中儿茶酚胺水平。非PD患者使用的抗抑郁药物包括三环类抗抑郁药(TCA)和选择性5-羟色胺(5-HT)再摄取抑制剂(SSRI),但仅对TCA在PD患者中的抗抑郁作用进行了仔细研究。电休克疗法已被证明对PD患者有抗抑郁疗效,经颅磁刺激在实验条件下可暂时缓解抑郁。在老年PD患者中,联合使用多种药物治疗抑郁的不良反应很常见。“5-羟色胺综合征”发生频率较高,因此司来吉兰不能与SSRI或TCA合用,抗帕金森病药物与抗抑郁药物之间的多种相互作用使PD患者的治疗策略更加复杂。本文描述了一种抑郁药物治疗的算法方法。