New Glucose-Lowering Agents for Diabetic Kidney Disease

被引:14
|
作者
de Vos, Lisanne C.
Hettige, Thushan S.
Cooper, Mark E.
机构
[1] Monash Univ, Dept Diabet, Cent Clin Sch, Melbourne, Vic, Australia
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Internal Med, Div Vasc Med, Groningen, Netherlands
关键词
Chronic kidney disease; GLP-1 receptor agonists; DPP-4; inhibitors; SGLT-2; Diabetes mellitus; GLUCAGON-LIKE PEPTIDE-1; DIPEPTIDYL PEPTIDASE-4 INHIBITORS; RENAL END-POINTS; BLOOD-PRESSURE; DOUBLE-BLIND; LONG-TERM; CARDIOVASCULAR OUTCOMES; POOLED ANALYSIS; SAFETY; EFFICACY;
D O I
10.1053/j.ackd.2018.01.002
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The prevalence of diabetes mellitus is increasing and is associated with a range of complications including nephropathy. New antidiabetic agents are sought which also have positive effects to diminish diabetic complications. Examples of promising new classes of such agents are glucagon-like peptide-1 receptor agonists, dipeptidyl peptidase-4 inhibitors, and sodium-glucose cotransporter 2 inhibitors. In addition to cardiovascular protective effects such as weight loss and decreased blood pressure of some of these agents, there is evidence for renoprotective effects with these agents. This review elaborates on the main results of renoprotective effects of these 3 treatment classes. In conclusion, currently available trials have demonstrated renoprotective effects for certain glucagon-like peptide-1 receptor agonists, liraglutide and semaglutide, and the sodium-glucose cotransporter 2 inhibitors, empagliflozin and canagliflozin. Dipeptidyl peptidase-4 inhibitors did not show a significant renoprotective effect. Nevertheless, larger studies with respect to renoprotective effects of these 3 drug classes are currently being performed, and thus, no conclusions for all of these agents can yet be made. Crown Copyright (C) 2018 Published by Elsevier Inc. on behalf of the National Kidney Foundation, Inc. All rights reserved.
引用
收藏
页码:149 / 157
页数:9
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