Mellen Philip B, Herrington David M
Department of Internal Medicine/Cardiology, Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157, USA.
J Hypertens. 2005 Jul;23(7):1311-25. doi: 10.1097/01.hjh.0000173510.52987.68.
PURPOSE IDENTIFICATION: Inter-individual variability in blood pressure response to treatment is well documented, but a clinically useful means to distinguish responders from non-responders has been elusive. With the advent of new technologies and genomic knowledge, more investigators are seeking to identify genetic determinants of blood pressure response to therapy.
We identified studies of candidate polymorphisms from an initial PubMed search using the MESH terms 'Hypertension: Drug Therapy' and 'Genetics' or 'Pharmacogenetics', limiting results to English-language publications on studies in human adults. We further identified specific polymorphisms of interest noted in earlier reviews and performed additional PubMed searches based on these candidate genes. Pertinent studies were further extracted from the references of studies already identified. We focused on clinical trials that measured blood pressure response to a medication or class of medications over a minimum of 4 weeks.
We evaluated studies looking at blood pressure response to commonly used classes of antihypertensive medications by major genetic variants. RESULTS OF ANALYSIS: Although many studies show that blood pressure response to a given class of antihypertensive medications varies by genotype for different polymorphisms, none of the genotypes identified consistently predicted blood pressure response.
Common variants may influence response to diuretics, beta-blockers, angiotensin-converting enzyme inhibitors, and angiotensin receptor blockers, but studies of polymorphisms have generally yielded conflicting results. The inclusion of pharmacogenomic studies in large clinical trials and other more innovative investigative methods may provide greater clarity of the potential role for genotyping in the treatment of patients with hypertension.
目的识别:血压对治疗反应的个体间差异已有充分记录,但区分反应者与无反应者的临床实用方法一直难以捉摸。随着新技术和基因组学知识的出现,越来越多的研究者试图确定血压对治疗反应的遗传决定因素。
我们通过使用医学主题词“高血压:药物治疗”和“遗传学”或“药物基因组学”在PubMed上进行初步检索,识别出候选多态性的研究,将结果限制为关于成年人类研究的英文出版物。我们进一步确定了早期综述中提到的感兴趣的特定多态性,并基于这些候选基因进行了额外的PubMed检索。相关研究从已识别研究的参考文献中进一步提取。我们关注的是至少持续4周测量血压对一种药物或一类药物反应的临床试验。
我们评估了通过主要基因变异研究血压对常用抗高血压药物类别的反应的研究。分析结果:尽管许多研究表明,对于不同的多态性,血压对某一类抗高血压药物的反应因基因型而异,但所识别的基因型均未一致预测血压反应。
常见变异可能影响对利尿剂、β受体阻滞剂、血管紧张素转换酶抑制剂和血管紧张素受体阻滞剂的反应,但多态性研究通常得出相互矛盾的结果。在大型临床试验中纳入药物基因组学研究和其他更具创新性的研究方法,可能会更清楚地阐明基因分型在高血压患者治疗中的潜在作用。