The Jerusalem Mental Health Center, Kfar Shaul Hospital, Hebrew University - Hadassah Medical School, Jerusalem, Israel.
Med Hypotheses. 2010 Dec;75(6):544-6. doi: 10.1016/j.mehy.2010.07.024. Epub 2010 Aug 12.
Parkinson disease (PD) is a chronic progressive degenerative disorder that affects over 6 million people worldwide. It is manifested by motor and psychiatric signs. The latter inflicts up to 88% of PD patients. With the prolongation of life expectancy, it is presumed that the prevalence of PD will further rise, together with comorbid depression. As a result, the need for an adequate therapeutic answer for compounded PD with depression is called for urgently. Several theories try to explain the trigger of depression in PD patients by impaired activity in dopamine, norepinephrine and serotonin systems. Various treatment to combat depressive symptoms in PD patients were proposed and are in use, with ambiguous results and disturbing side effects. These anti-depressive modalities include SSRI's, SNRI, TCA, NRI and ECT. Dopamine agonists showed some anti-depressant activity in several studies in depressive PD, but may cause side effects such as dizziness, somnolence, confusion and even hallucinations. The role of dopamine agonists in the treatment of depression is still being explored because of no sufficient number of controlled studies in this area. Our hypothesis is to suggest NDRI - Bupropion - as the first line of treatment in PD patients with depression, in PD induced depression and/or in depression triggered by one of the treatments given for PD. Dual norepinephrine and dopamine reuptake inhibition is associated with unique clinical profile that compounds together anti-depressant efficacy without serotonin associated side effects such as weight gain, sedation, sexual dysfunction. Bupropion, as mainly dopaminergic and noradrenergic anti-depressant can alleviate therapeutically depressive symptoms associated with PD. Clinical controlled studies on Bupropion use in PD depressed patients are required to support this hypothesis.
帕金森病(PD)是一种慢性进行性退行性疾病,影响全球超过 600 万人。它表现为运动和精神症状。后者影响多达 88%的 PD 患者。随着预期寿命的延长,预计 PD 的患病率将进一步上升,同时伴有合并抑郁。因此,迫切需要为伴有抑郁的复合 PD 提供足够的治疗方法。几种理论试图通过多巴胺、去甲肾上腺素和血清素系统活性受损来解释 PD 患者抑郁的触发机制。已经提出并正在使用各种治疗方法来对抗 PD 患者的抑郁症状,但结果模棱两可,副作用令人不安。这些抗抑郁模式包括 SSRI、SNRI、TCA、NRI 和 ECT。多巴胺激动剂在几项针对抑郁性 PD 患者的研究中显示出一些抗抑郁活性,但可能引起头晕、嗜睡、意识混乱甚至幻觉等副作用。由于该领域缺乏足够数量的对照研究,多巴胺激动剂在治疗抑郁症中的作用仍在探索中。我们的假设是建议将 NDRI-安非他酮-作为 PD 伴抑郁患者、PD 引起的抑郁和/或 PD 治疗之一引起的抑郁的一线治疗药物。双重去甲肾上腺素和多巴胺再摄取抑制与独特的临床特征相关联,这种特征结合在一起具有抗抑郁疗效,而没有与体重增加、镇静、性功能障碍等相关的血清素副作用。安非他酮作为主要的多巴胺能和去甲肾上腺素能抗抑郁药,可以缓解与 PD 相关的治疗性抑郁症状。需要进行关于安非他酮在 PD 抑郁患者中使用的临床对照研究来支持这一假设。