Department of Cardionephrology, University of Genoa, Azienda Ospedaliera Universitaria San Martino, Viale Benedetto XV 6, Genoa, Italy.
Curr Pharm Des. 2012;18(7):971-80. doi: 10.2174/138161212799436520.
Chronic kidney disease has become a major public health problem worldwide mainly as a consequence of the emerging epidemic of hypertension, diabetes, and obesity. It is currently estimated that nearly 15% of the general population has some degree of renal damage, a figure that reaches 50% in at-risk subgroups. Renin-angiotensin-aldosterone system (RAAS) inhibitors represent the agents of choice to control hypertension and reduce urinary albumin excretion, thereby delaying renal function deterioration. Greater blockade of the RAAS either by the combined use of multiple drugs or by supramaximal doses of single agents may provide greater renal protection. Furthermore, it has been proposed especially in the presence of proteinuria. However, at this time there is insufficient evidence to routinely recommend this therapeutic approach in patients with chronic kidney disease. The present article examines the currently available evidence and practical implications of pharmacological disruption of RAAS activity for renal protection.
慢性肾脏病已成为全球主要的公共卫生问题,主要是由于高血压、糖尿病和肥胖症的流行。目前估计,将近 15%的普通人群存在一定程度的肾脏损伤,而在高危亚组中,这一数字达到 50%。肾素-血管紧张素-醛固酮系统(RAAS)抑制剂是控制高血压和减少尿蛋白排泄,从而延缓肾功能恶化的首选药物。通过联合使用多种药物或使用单药的超最大剂量,更大程度地阻断 RAAS,可能会提供更大的肾脏保护。此外,在存在蛋白尿的情况下尤其如此。然而,目前尚无足够的证据常规推荐这种治疗方法用于慢性肾脏病患者。本文探讨了目前关于 RAAS 活性的药理学干预对肾脏保护的证据和实际意义。