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一名慢性心力衰竭且携带CYP2D6*1/*5基因的患者出现危及生命的血清素综合征。

Life-threatening serotonin syndrome in a patient with chronic heart failure and CYP2D6*1/*5.

作者信息

Sato Akinori, Okura Yuji, Minagawa Shiroh, Ohno Yukiko, Fujita Satoru, Kondo Daisuke, Hayashi Manabu, Komura Satoru, Kato Kiminori, Hanawa Haruo, Kodama Makoto, Aizawa Yoshifusa

机构信息

Division of Cardiology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

出版信息

Mayo Clin Proc. 2004 Nov;79(11):1444-8. doi: 10.4065/79.11.1444.

Abstract

We report a case of serotonin syndrome that occurred in a patient with chronic heart failure associated with a panic disorder. The 39-year-old Japanese man had been treated with paroxetine at 20 mg/d for 1 1/2 years. He presented with rhabdomyolysis, renal failure, fulminant liver failure, cardiac conduction disturbance, and disseminated intravascular coagulation, as well as conventional symptoms of serotonin syndrome including alterations in cognition (disorientation, confusion) and behavior (restlessness), autonomic nervous system dysfunction (fever, shivering), and abnormal neuromuscular activity (ataxia, hyperreflexia, myoclonus). All medications prescribed before hospital admission were discontinued. After 24 hours of continuous venovenous hemofiltration, diuresis resumed and renal and liver function improved rapidly. Disorientation, restlessness, hyperreflexia, and myoclonus abated slowly over the next 72 hours. The patient's anxiety subsided more slowly, and he recovered completely 1 week later. The plasma concentration of paroxetine was elevated far above the upper limit of the therapeutic range. The patient had cytochrome P-450 (CYP) 2D6*1/*5, a heterozygosity of an inactivated allele of CYP2D6, which metabolizes paroxetine. The patient was determined to be an intermediate metabolizer who was potentially vulnerable to paroxetine, a major inhibitor of CYP2D6. Heart failure is often accompanied by psychiatric disorders. A wide range of drugs commonly prescribed for these conditions, including beta-blockers, antiarrhythmics, and antidepressants, are metabolized by CYP2D6. Genetic screening for CYP2D6 in patients with these conditions may prevent life-threatening drug intoxication.

摘要

我们报告了一例发生在患有慢性心力衰竭并伴有惊恐障碍患者身上的血清素综合征病例。这位39岁的日本男性服用帕罗西汀20毫克/天,持续了1年半。他出现了横纹肌溶解、肾衰竭、暴发性肝衰竭、心脏传导障碍和弥散性血管内凝血,以及血清素综合征的传统症状,包括认知改变(定向障碍、意识混乱)和行为改变(烦躁不安)、自主神经系统功能障碍(发热、寒战)以及异常神经肌肉活动(共济失调、反射亢进、肌阵挛)。入院前开具的所有药物均停用。经过24小时的持续静脉-静脉血液滤过,尿量恢复,肾功能和肝功能迅速改善。定向障碍、烦躁不安、反射亢进和肌阵挛在接下来的72小时内逐渐减轻。患者的焦虑缓解得更慢,1周后完全康复。帕罗西汀的血浆浓度远高于治疗范围的上限。该患者具有细胞色素P-450(CYP)2D6*1/*5,这是代谢帕罗西汀的CYP2D6失活等位基因的杂合子。该患者被确定为中间代谢者,可能对作为CYP2D6主要抑制剂的帕罗西汀敏感。心力衰竭常伴有精神障碍。常用于这些病症的多种药物,包括β受体阻滞剂、抗心律失常药和抗抑郁药,均由CYP2D6代谢。对这些病症患者进行CYP2D6基因筛查可能预防危及生命的药物中毒。

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