医学
药品
药物遗传学
疾病
不利影响
药理学
血管紧张素转换酶
药物治疗
生物信息学
抗高血压药
遗传变异
内科学
基因型
遗传学
生物
血压
基因
作者
Jana El Cheikh,Fatima Omer Hamed,Hana Rifi,Ali Dakroub,Ali H. Eid
摘要
Abstract Hypertension is a major contributor to cardiovascular disease and its associated morbidity and mortality. The low efficacy observed with some anti‐hypertensive therapies has been attributed partly to inter‐individual genetic variability. This paper reviews the major findings regarding these genetic variabilities that modulate responses to anti‐hypertensive therapies such as angiotensin converting enzyme (ACE) inhibitors, angiotensin receptor blockers (ARBs), diuretics, calcium channel blockers (CCBs) and β‐adrenoceptor blockers. The importance of studying these genetic polymorphisms stems from the goal to optimise anti‐hypertensive therapy for each individual patient, aiming for the highest efficacy and lowest risk of adverse effects. It is important to recognise that environmental and epigenetic factors can contribute to the observed variations in drug responses. Owing to the multigenic and multifactorial nature of drug responses, further research is crucial for translating these findings into clinical practice and the establishment of reliable recommendations.
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