Department of Clinical Pharmacology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Br J Clin Pharmacol. 2013 Oct;76(4):536-50. doi: 10.1111/bcp.12195.
Chronic kidney disease (CKD) is a worldwide health problem. The disease is most often progressive of nature with a high impact on patients and society. It is increasingly recognized that CKD can be detected in the early stages and should be managed as early as possible. Treatment of the cause, but in particular control of the main risk markers, such as high blood pressure, glucose and albuminuria, has been instrumental in delaying the progression to end-stage renal disease (ESRD). However, despite the state of the art therapy, the absolute risk of renal and cardiovascular morbidity and mortality in CKD patients remains devastatingly high. Novel drugs are therefore highly desirable to halt effectively the progressive renal (and cardiovascular) function loss. Recently, several novel strategies have been tested targeting traditional risk factors such as blood pressure (combination therapy of angiotensin converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARB) and novel mineralocorticoid receptor antagonists) as well as dyslipidaemia (statins) with surprising results. In addition, drug targets specifically related to the kidney, such as vitamin D, uric acid, erythropoietin and phosphate, have been the subject of clinical trials, in some instances with unexpected results. Finally, novel targets including endothelin receptors and inflammatory pathways are increasingly explored as potential avenues to improve renal and cardiovascular protection, albeit that the drugs tested have not been unequivocally successful. In this article we review novel drugs or intervention strategies for the management of CKD, we try to provide explanations for the failure of some promising drugs and hypothesize on the potential success of new strategies.
慢性肾脏病(CKD)是一个全球性的健康问题。该疾病通常呈进行性发展,对患者和社会的影响很大。越来越多的人认识到,CKD 可以在早期被发现,应该尽早进行管理。治疗病因,但特别是控制主要的风险标志物,如高血压、葡萄糖和蛋白尿,有助于延缓进展为终末期肾病(ESRD)。然而,尽管有了最先进的治疗方法,CKD 患者的肾脏和心血管发病率和死亡率的绝对风险仍然高得惊人。因此,非常需要新型药物来有效地阻止肾脏(和心血管)功能的进行性丧失。最近,已经测试了几种针对传统风险因素的新策略,如血压(血管紧张素转换酶抑制剂(ACEi)和血管紧张素受体阻滞剂(ARB)的联合治疗以及新型的盐皮质激素受体拮抗剂)和血脂异常(他汀类药物),结果令人惊讶。此外,与肾脏有关的药物靶点,如维生素 D、尿酸、促红细胞生成素和磷酸盐,也已成为临床试验的主题,在某些情况下,结果出人意料。最后,包括内皮素受体和炎症途径在内的新靶点也越来越多地被探索作为改善肾脏和心血管保护的潜在途径,尽管测试的药物并不完全成功。在本文中,我们综述了用于 CKD 管理的新型药物或干预策略,我们试图解释一些有前途的药物的失败,并假设新策略的潜在成功。