Majewski Collen, Bakris George L
Department of Medicine, Section of Endocrinology, Diabetes and Metabolism, ASH Comprehensive Hypertension Center, The University of Chicago Medicine, 5841 S. Maryland Ave. MC 1027, Chicago, IL, 60637, USA.
Curr Diab Rep. 2016 Apr;16(4):24. doi: 10.1007/s11892-016-0713-y.
Medications that block the renin-angiotensin-aldosterone system (RAAS) are a cornerstone of diabetic nephropathy treatment. These agents play an important role in slowing the nephropathy progression in patients with diabetes. Clinical outcome trials that investigated use of these drug classes in patients with diabetic nephropathy have demonstrated clinical significant benefit in slowing nephropathy progression only in people with >300 mg/day of proteinuria. Thus, guidelines mandate their use in such patients. Conversely, combinations of RAAS blocking agents in these patients can worsen renal outcomes. Moreover, use of RAAS blockers in patients with a glomerular filtration rate below 45 mL/min/1.73 m(2) is limited by hyperkalemia. New agents that predictably bind excess potassium in the colon offer the possibility of extending RAAS inhibitor use in advanced chronic kidney disease (CKD) to allow evaluation of RAAS blockade for nephropathy and cardiovascular outcomes. These new potassium-binding agents may provide an opportunity to continue full-dose RAAS inhibition and assess if the benefits of RAAS blockade seen in stage 3 CKD can be extrapolated to persons with stages 4 and 5 CKD, not previously tested due to hyperkalemia.
阻断肾素-血管紧张素-醛固酮系统(RAAS)的药物是糖尿病肾病治疗的基石。这些药物在减缓糖尿病患者的肾病进展方面发挥着重要作用。针对糖尿病肾病患者使用这些药物类别的临床结局试验表明,仅在蛋白尿>300mg/天的患者中,减缓肾病进展具有临床显著益处。因此,指南规定在这类患者中使用这些药物。相反,这些患者联合使用RAAS阻断剂会使肾脏结局恶化。此外,肾小球滤过率低于45mL/min/1.73m²的患者使用RAAS阻滞剂会受到高钾血症的限制。可预测地结合结肠中过量钾的新型药物为在晚期慢性肾脏病(CKD)中扩大RAAS抑制剂的使用提供了可能性,以便评估RAAS阻断对肾病和心血管结局的影响。这些新型钾结合剂可能提供一个机会,继续进行全剂量RAAS抑制,并评估在3期CKD中看到的RAAS阻断益处是否可以外推到4期和5期CKD患者,此前由于高钾血症尚未对其进行测试。