期刊
JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS
卷 44, 期 5, 页码 823-828出版社
WILEY
DOI: 10.1111/jcpt.12838
关键词
8-isoprostaglandin F2 alpha; aspirin resistance; cardiovascular and cerebrovascular disease; oxidative stress; platelet activation; thromboxane A2
What is Known and Objective Aspirin resistance refers to a patient's poor response to aspirin. There are many factors that can contribute to aspirin resistance, including single-nucleotide polymorphisms, medication compliance, drug-drug interactions and inflammation. Comment Recently, oxidative stress-induced 8-isoprostaglandin F2 alpha has attracted considerable attention because it is considered as a mechanism of aspirin resistance in many diseases, including coronary artery disease, neurology system disease, metabolic syndrome, cancer, chronic obstructive pulmonary disease and chronic kidney disease. In these diseases, increased oxidative stress may promote platelet activation and reduce the efficacy of aspirin by producing excessive amounts of 8-isoprostaglandin F2 alpha. What is New and Conclusion Given the wide clinical use of aspirin, it is essential to understand why some patients do not response to it. This article reviews current research on aspirin resistance mediated by oxidative stress-induced 8-isoprostaglandin F2 alpha.
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