AI Article Synopsis

  • Cardiac dysfunction is a leading cause of death in cancer survivors, and cardiotoxicity from treatments poses significant risks influenced by factors like age, obesity, and pre-existing heart conditions.
  • Troponin is an important biomarker for identifying cardiac issues, particularly in patients undergoing chemotherapy with agents like anthracyclines and herceptin, showing effectiveness in diagnosing cardiotoxicity.
  • Current guidelines suggest monitoring troponin levels based on individual risk factors and treatment type, though optimal cut-off values for this biomarker are still being studied.

Article Abstract

In cancer survivors, cardiac dysfunction is the main cause of mortality. Cardiotoxicity represents a decline in cardiac function associated with cancer therapy, and the risk factors include smoking, dyslipidemia, an age of over 60 years, obesity, and a history of coronary artery disease, diabetes, atrial fibrillation, or heart failure. Troponin is a biomarker that is widely used in the detection of acute coronary syndromes. It has a high specificity, although it is not exclusively associated with myocardial ischemia. The aim of this paper is to summarize published studies and to establish the role of troponin assays in the diagnosis of cardiotoxicity associated with various chemotherapeutic agents. Troponin has been shown to be a significant biomarker in the diagnosis of the cardiac dysfunction associated with several types of chemotherapeutic drugs: anthracyclines, anti-human epidermal growth factor receptor 2 treatment, and anti-vascular endothelial growth factor therapy. Based on the data available at this moment, troponin is useful for baseline risk assessment, the diagnosis of cardiotoxicity, and as a guide for the initiation of cardioprotective treatment. There are currently clear regulations regarding the timing of troponin surveillance depending on the patient's risk of cardiotoxicity and the type of medication administered, but data on the cut-off values of this biomarker are still under investigation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410123PMC
http://dx.doi.org/10.3390/life12081183DOI Listing

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