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September 18, 2025Clinical Toxicology4 citations

Cardiovascular toxicity associated with supplement use

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JCJustin Corcoran

Key Points

  • Cardiovascular toxicity can arise from various supplements through mechanisms like ion channel poisoning, leading to serious outcomes.
  • Adverse effects include tachycardia, hypertension, and myocardial infarction, often linked to specific components like stimulants or steroids.
  • Inhibition of cardiac ion channels has been associated with certain supplements, which can result in life-threatening dysrhythmias.
  • Clinicians must be aware of the potential for serious cardiovascular events related to supplement use, despite their rarity.

Abstract

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

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Cite This Study

Justin Corcoran (2025) studied this question.

synapsesocial.com/papers/68d461c231b076d99fa60e3dhttps://doi.org/10.1080/15563650.2025.2550983
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