Cardiovascular toxicity associated with supplement use.

IF 3.3
Justin Corcoran
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Abstract

Background: Supplement use is prevalent and appears to be increasing over time. In the United States, regulation by the Food and Drug Administration is limited largely to post-marketing surveillance, raising safety concerns. A variety of supplements have been associated with cardiovascular toxicity, which can occur via adulteration, substitution, or as a result of intrinsic toxicity of the supplement. Cardiovascular toxicity due to supplement use may arise via several different mechanisms, and has been reported with supplements that act as central nervous system stimulants, via poisoning of cardiac ion channels, as a result of cardioactive steroids, and by modulation of the endocrine system.

Stimulants: Supplements that act as central nervous system stimulants include those that act directly on adrenoreceptors or indirectly via the release of catecholamines, and include substances such as ephedra, synephrine, and yohimbine. Adverse effects vary depending on the agent and include tachycardia, hypertension, hyperthermia, myocardial infarction, and cardiac arrest.

Ion channel poisons: Poisoning of cardiac voltage-gated sodium channels has been reported with supplements that contain or are contaminated with aconitine or grayanotoxins and cause wide complex dysrhythmias. Inhibition of cardiac myocyte voltage-gated potassium channels is associated with berberine, leading to prolongation of the QT interval and polymorphic ventricular tachycardia.

Cardioactive steroids: Cardioactive steroids derived from yellow oleander are implicated in serious toxicity and death associated with the weight loss product "Nuez de la India" in what appears to be an inadvertent substitution error. Animal-derived cardioactive steroids from the Bufo spp. of toad used as an aphrodisiac also cause clinically significant cardiac toxicity and death.

Endocrine modulators: Supplemental use of black licorice induces hypokalemia, and is associated with the development of torsade de pointes.

Conclusion: Clinically significant cardiovascular toxicity associated with supplement use is a fortunately rare phenomenon that can occur via multiple mechanisms. Clinicians should maintain awareness that supplements may produce serious and sometimes life-threatening cardiovascular poisoning.

与补充剂使用相关的心血管毒性。
背景:补充剂的使用是普遍的,并且似乎随着时间的推移而增加。在美国,食品和药物管理局(Food and Drug Administration)的监管主要局限于上市后的监督,这引发了人们对安全性的担忧。各种补充剂都与心血管毒性有关,这可能通过掺假、替代或补充剂的内在毒性发生。服用补品引起的心血管毒性可能通过几种不同的机制产生,据报道,补品作为中枢神经系统兴奋剂,通过心脏离子通道中毒,作为心脏活性类固醇的结果,以及通过调节内分泌系统。兴奋剂:作为中枢神经系统兴奋剂的补充剂包括那些直接作用于肾上腺受体或通过释放儿茶酚胺间接作用的补充剂,包括麻黄、辛弗林和育亨宾等物质。不良反应因药物而异,包括心动过速、高血压、高热、心肌梗死和心脏骤停。离子通道中毒:已报道含有或被乌头碱或灰色毒素污染的补充剂引起心脏电压门控钠通道中毒,并引起广泛的复杂心律失常。抑制心肌细胞电压门控钾通道与小檗碱有关,导致QT间期延长和多态性室性心动过速。心脏活性类固醇:从黄夹竹桃中提取的心脏活性类固醇涉及与减肥产品“Nuez de la India”相关的严重毒性和死亡,这似乎是一个无意的替代错误。从蟾蜍的Bufo家族提取的动物源性心脏活性类固醇用作壮阳药也会引起临床上显著的心脏毒性和死亡。内分泌调节剂:补充使用黑甘草诱导低钾血症,并与扭转点的发展有关。结论:与补充剂使用相关的临床显著心血管毒性是一种幸运的罕见现象,可能通过多种机制发生。临床医生应该意识到补充剂可能会导致严重的,有时甚至危及生命的心血管中毒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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