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DOI 10.1016/j.ejphar.2024.176907

Медицинская библиотека · European journal of pharmacology · 2024

Pharmacogenetics of angiotensin-converting enzyme inhibitors (ACEI) and angiotensin II receptor blockers (ARB) in cardiovascular diseases.

Agostini Lívia da Cunha, Silva Nayara Nascimento Toledo, Belo Vanessa de Almeida, Luizon Marcelo Rizzatti, Lima Angelica Alves, da Silva Glenda Nicioli

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Аннотация

Cardiovascular diseases (CVDs) have a high mortality rate, and despite the several available therapeutic targets, non-response to antihypertensives remains a common problem. Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) are important classes of drugs recommended as first-line therapy for several CVDs. However, response to ACEIs and ARBs varies among treated patients. Pharmacogenomics assesses how an individual's genetic characteristics affect their likely response to drug therapy. Currently, numerous studies suggest that genetic polymorphisms may contribute to variability in drug response. Moreover, further studies evaluating gene-gene interactions within signaling pathways in response to antihypertensives might help to unravel potential genetic predictors for antihypertensive response. This review summarizes the pharmacogenetic data for ACEIs and ARBs in patients with CVD, and discusses the potential pharmacogenetics of these classes of antihypertensives in clinical practice. However, replication studies in different populations are needed. In addition, studies that evaluate gene-gene interactions that share signaling pathways in the response to antihypertensive drugs might facilitate the discovery of genetic predictors for antihypertensive response.

Для цитирования: Agostini Lívia da Cunha, Silva Nayara Nascimento Toledo, Belo Vanessa de Almeida, Luizon Marcelo Rizzatti, Lima Angelica Alves, da Silva Glenda Nicioli. Pharmacogenetics of angiotensin-converting enzyme inhibitors (ACEI) and angiotensin II receptor blockers (ARB) in cardiovascular diseases.. European journal of pharmacology. 2024. DOI: 10.1016/j.ejphar.2024.176907.

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