Praetner Marc, Schiele Timo, Werle Lukas, Kuffer Janina, Nischwitz Sandra, Keck Martin E, Kloiber Stefan
Walter Brendel Center of Experimental Medicine, Ludwig-Maximilians-Universität München, Marchioninistr. 15, 81377 Munich, Germany.
Psychosomatische Klinik Kloster Dießen GmbH & Co. KG, Klosterhof 20, 86911 Dießen am Ammersee, Germany.
Case Rep Psychiatry. 2021 Mar 1;2021:8868023. doi: 10.1155/2021/8868023. eCollection 2021.
The pharmacological treatment options of Parkinson's disease (PD) have considerably evolved during the last decades. However, therapeutic regimes are complicated due to individual differences in disease progression as well as the occurrence of complex nonmotor impairments such as mood and anxiety disorders. Antidepressants in particular are commonly prescribed for the treatment of depressive symptoms and anxiety in PD. . In this case report, we describe a case of a 62-year-old female patient with PD and history of depressive symptoms for which she had been treated with moclobemide concurrent with anti-Parkinson medications pramipexole, rasagiline, and L-DOPA+benserazide retard. An increase in the dosage of moclobemide 12 months prior to admission progressively led to serotonergic overstimulation and psychovegetative exacerbations mimicking the clinical picture of an anxiety spectrum disorder. After moclobemide and rasagiline were discontinued based on the hypothesis of serotonergic overstimulation, the patient's psychovegetative symptoms subsided.
The specific pharmacological regime in this case probably caused drug-drug interactions resulting in a plethora of psychovegetative symptoms. Likely due to the delayed onset of adverse effects, physicians had difficulties in determining the pharmacologically induced serotonin toxicity. This case report emphasizes the complexity of pharmacological treatments and the importance of drug-drug interaction awareness in the treatment of PD patients with complicating nonmotor dysfunctions such as depression.
在过去几十年中,帕金森病(PD)的药物治疗选择有了很大进展。然而,由于疾病进展的个体差异以及复杂的非运动障碍(如情绪和焦虑障碍)的出现,治疗方案变得复杂。特别是抗抑郁药通常用于治疗PD患者的抑郁症状和焦虑。在本病例报告中,我们描述了一名62岁女性PD患者,她有抑郁症状病史,曾同时服用吗氯贝胺与抗帕金森药物普拉克索、雷沙吉兰以及左旋多巴+苄丝肼缓释片进行治疗。入院前12个月吗氯贝胺剂量增加逐渐导致血清素过度刺激和拟似焦虑谱系障碍临床表现的精神植物神经症状加重。基于血清素过度刺激的假设停用吗氯贝胺和雷沙吉兰后,患者的精神植物神经症状消退。
本病例中的特定药物治疗方案可能导致药物相互作用,从而引发大量精神植物神经症状。可能由于不良反应的延迟发作,医生难以确定药物引起的血清素毒性。本病例报告强调了药物治疗的复杂性以及在治疗伴有抑郁等复杂非运动功能障碍的PD患者时了解药物相互作用的重要性。