GLP-1 receptor agonists in diabetic kidney disease: from the patient-side to the bench-side

被引:35
作者
Dieter, Brad P. [1 ]
Alicic, Radica Z. [1 ,2 ]
Tuttle, Katherine R. [1 ,2 ,3 ,4 ]
机构
[1] Providence Hlth Care, Providence Med Res Ctr, Spokane, WA USA
[2] Univ Washington, Dept Med, Nephrol Div, Spokane, WA USA
[3] Kidney Res Inst, Spokane, WA USA
[4] Univ Washington, Inst Translat Hlth Sci, Spokane, WA USA
关键词
albuminuria; anti-inflammatory therapy; diabetes; end-stage renal disease; GLUCAGON-LIKE PEPTIDE-1; BLOOD-PRESSURE; UNITED-STATES; HEART-RATE; LIRAGLUTIDE; EXENDIN-4; EXENATIDE; NEPHROPATHY; OUTCOMES; SYSTEM;
D O I
10.1152/ajprenal.00211.2018
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Diabetic kidney disease (DKD), one of the most common and severe microvascular complications of diabetes, is the leading cause of chronic kidney disease and end-stage kidney disease worldwide. Since the development of renin-angiotensin system inhibition nearly three decades ago, no new therapeutic agents have received regulatory approval for treatment of DKD. Glucagon-like peptide-1 (GLP-1) receptor agonists, a class of newer antihyperglycemic agents, have shown promise for prevention of DKD onset and progression. This perspective summarizes clinical and experimental observations to give insight into biological mechanisms beyond glycemic control, such as natriuresis and anti-inflammatory actions, for preservation of kidney function in patients with diabetes.
引用
收藏
页码:F1519 / F1525
页数:7
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