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尽早控制:口服降糖药假定的肾脏保护血流动力学效应

Beat it early: putative renoprotective haemodynamic effects of oral hypoglycaemic agents.

作者信息

Gnudi Luigi, Karalliedde Janaka

机构信息

Cardiovascular Division, Department of Diabetes and Endocrinology, School of Life Science & Medicine, King's College, London, UK.

出版信息

Nephrol Dial Transplant. 2016 Jul;31(7):1036-43. doi: 10.1093/ndt/gfv093. Epub 2015 Apr 8.

Abstract

Diabetic kidney disease represents a considerable burden; around one-third of patients with type 2 diabetes develop chronic kidney disease. In health, the kidneys play an important role in the regulation of glucose homeostasis via glucose utilization, gluconeogenesis and glucose reabsorption. In patients with diabetes, renal glucose homeostasis is significantly altered with an increase in both gluconeogenesis and renal tubular reabsorption of glucose. Environmental factors, both metabolic (hyperglycaemia, obesity and dyslipidaemia) and haemodynamic, together with a genetic susceptibility, lead to the activation of pro-oxidative, pro-inflammatory and pro-fibrotic pathways resulting in kidney damage. Hyperfiltration and its haemodynamic-driven insult to the kidney glomeruli is an important player in proteinuria and progression of kidney disease towards end-stage renal failure. Control of glycaemia and blood pressure are the mainstays to prevent kidney damage and slow its progression. There is emerging evidence that some hypoglycaemic agents may have renoprotective effects which are independent of their glucose-lowering effects. Sodium-glucose co-transporter-2 (SGLT-2) inhibitors may exert a renoprotective effect by a number of mechanisms including restoring the tubuloglomerular feedback mechanism and lowering glomerular hyperfiltration, reducing inflammatory and fibrotic markers induced by hyperglycaemia thus limiting renal damage. Simultaneous use of an SGLT-2 inhibitor and blockade of the renin-angiotensin-aldosterone system may be a strategy to slow progression of diabetic nephropathy more than either drug alone. The use of dipeptidyl peptidase-4 inhibitors and glucagon-like peptide 1 receptor agonists may exert a renoprotective effect by reducing inflammation, fibrosis and blood pressure. Given the burden of diabetic kidney disease, any additional renoprotective benefit with hypoglycaemic therapy is to be welcomed. Large randomized controlled trials are currently underway investigating if these new anti-diabetic agents can provide renoprotection in diabetes.

摘要

糖尿病肾病是一个相当大的负担;约三分之一的2型糖尿病患者会发展为慢性肾病。在健康状态下,肾脏通过葡萄糖利用、糖异生和葡萄糖重吸收在调节葡萄糖稳态中发挥重要作用。在糖尿病患者中,肾葡萄糖稳态会发生显著改变,糖异生和肾小管对葡萄糖的重吸收均增加。代谢(高血糖、肥胖和血脂异常)和血流动力学等环境因素,以及遗传易感性,会导致促氧化、促炎和促纤维化途径的激活,从而造成肾脏损伤。高滤过及其对肾小球的血流动力学驱动性损伤是蛋白尿和肾病进展至终末期肾衰竭的一个重要因素。控制血糖和血压是预防肾脏损伤并减缓其进展的主要措施。新出现的证据表明,一些降糖药物可能具有独立于其降糖作用的肾脏保护作用。钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂可能通过多种机制发挥肾脏保护作用,包括恢复球管反馈机制和降低肾小球高滤过、减少高血糖诱导的炎症和纤维化标志物,从而限制肾脏损伤。同时使用SGLT-2抑制剂和阻断肾素-血管紧张素-醛固酮系统可能是一种比单独使用任何一种药物都更能减缓糖尿病肾病进展的策略。使用二肽基肽酶-4抑制剂和胰高血糖素样肽1受体激动剂可能通过减轻炎症、纤维化和降低血压来发挥肾脏保护作用。鉴于糖尿病肾病的负担,降糖治疗带来的任何额外肾脏保护益处都值得欢迎。目前正在进行大型随机对照试验,以研究这些新型抗糖尿病药物是否能为糖尿病患者提供肾脏保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0214/4917060/792e17318f51/gfv09301.jpg

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