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度洛西汀诱发老年2型糖尿病伴疼痛性糖尿病神经病变患者抗利尿激素分泌异常综合征的快速发作

Rapid onset of syndrome of inappropriate antidiuretic hormone secretion induced by duloxetine in an elderly type 2 diabetic patient with painful diabetic neuropathy.

作者信息

Kamei Shinji, Kaneto Hideaki, Tanabe Akihito, Irie Shintaro, Hirata Yurie, Shimoda Masashi, Kohara Kenji, Mune Tomoatsu, Kaku Kohei

机构信息

Division of Diabetes, Metabolism and Endocrinology, Kawasaki Medical School Kurashiki, Japan.

出版信息

J Diabetes Investig. 2015 May;6(3):343-5. doi: 10.1111/jdi.12301. Epub 2014 Dec 29.

DOI:10.1111/jdi.12301
PMID:25969720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4420567/
Abstract

Diabetic neuropathy is the most common diabetic complication. Duloxetine, a serotonin noradrenaline reuptake inhibitor (SNRI), is widely used for the treatment of diabetic painful neuropathy (DPN) because of the efficacy and safety profile. Syndrome of inappropriate antidiuretic hormone secretion, which is strongly associated duloxetine, is a rare but occasionally life-threatening adverse effect. Here, we report a case of syndrome of inappropriate antidiuretic hormone secretion that rapidly developed after starting duloxetine in an elderly Japanese female type 2 diabetes mellitus patient. Furthermore, we discuss the possible relationship between the onset of syndrome of inappropriate antidiuretic hormone secretion and the gene polymorphism of cytochrome P450 isoform 1A2 and 2D6, both of which are responsible for duloxetine metabolism.

摘要

糖尿病神经病变是最常见的糖尿病并发症。度洛西汀是一种5-羟色胺去甲肾上腺素再摄取抑制剂(SNRI),因其疗效和安全性而被广泛用于治疗糖尿病性疼痛性神经病变(DPN)。与度洛西汀密切相关的抗利尿激素分泌异常综合征是一种罕见但偶尔会危及生命的不良反应。在此,我们报告一例老年日本2型糖尿病女性患者在开始使用度洛西汀后迅速发生抗利尿激素分泌异常综合征的病例。此外,我们还讨论了抗利尿激素分泌异常综合征的发病与细胞色素P450同工酶1A2和2D6基因多态性之间的可能关系,这两种同工酶均参与度洛西汀的代谢。

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A poor metabolizer of both CYP2C19 and CYP2D6 identified by mechanistic pharmacokinetic simulation in a fatal drug poisoning case involving venlafaxine.在涉及文拉法辛的一起致命药物中毒案例中,通过机制药代动力学模拟鉴定出同时为 CYP2C19 和 CYP2D6 弱代谢型的个体。
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Duloxetine is both an inhibitor and a substrate of cytochrome P4502D6 in healthy volunteers.在健康志愿者中,度洛西汀既是细胞色素P4502D6的抑制剂,也是其底物。
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