Expert Insights for PCPs in Managing CKD in T2DM

Yik Tian Akira Wu
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Abstract

Diabetic kidney disease (DKD) is the most common cause of end-stage renal disease (ESRD) in most developed countries including Singapore. Patients with DKD have a disproportionately higher risk for cardiovascular (CV) events and mortality. A comprehensive strategy is recommended for management of patients with DKD to reduce the risks of kidney disease progression and CV disease. Lifestyle modification, CV risk factor and glycaemic control, and maximum tolerated renin-angiotensin-aldosterone-system (RAAS) blockade form the foundation of DKD care. The kidney-protective effects of sodium-glucose co-transporter 2 (SGLT2) inhibitors are well established by randomised controlled trials (RTCs) in patients with DKD, and are independent of the stage of kidney disease. Glucagon-like peptide-1 receptor agonist (GLP-1RA) is the preferred added agent to metformin and SGLT-2 inhibitor if individualised glycaemic targets are not achieved. In addition, the non-steroidal mineralocorticoid receptor antagonist (MRA) finerenone improves kidney and cardiovascular outcomes in patients with DKD.
PCPs在T2DM CKD管理中的专家见解
在包括新加坡在内的大多数发达国家,糖尿病肾病(DKD)是终末期肾病(ESRD)最常见的原因。DKD患者发生心血管(CV)事件和死亡率的风险不成比例地高。建议对DKD患者进行综合管理,以降低肾脏疾病进展和心血管疾病的风险。生活方式改变,心血管危险因素和血糖控制,最大耐受性肾素-血管紧张素-醛固酮系统(RAAS)阻断是DKD护理的基础。钠-葡萄糖共转运蛋白2 (SGLT2)抑制剂的肾脏保护作用在DKD患者的随机对照试验(rtc)中得到了很好的证实,并且与肾脏疾病的分期无关。如果个体化降糖目标无法实现,胰高血糖素样肽-1受体激动剂(GLP-1RA)是二甲双胍和SGLT-2抑制剂的首选添加剂。此外,非甾体矿物皮质激素受体拮抗剂(MRA)细烯酮可改善DKD患者的肾脏和心血管预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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