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New hypoglycemic agents and the kidney: what do the major trials tell us?
Brendan Smyth1, Vlado Perkovic1
1The George Institute for Global Health, UNSW, Sydney, Australia.
Abstract:
As the burden of diabetic kidney disease continues to expand, new therapies to preserve renal function or prevent diabetic nephropathy are urgently needed. In the past decade, a number of new hypoglycemic classes have emerged, each with a unique profile of action and benefits. Here we review the impact of glycemic control on renal outcomes and the results of the major clinical trials of glucagon-like peptide 1 (GLP-1) agonists, dipeptidyl peptidase-4 (DPP-4) inhibitors, and sodium-glucose co-transporter 2 (SGLT2) inhibitors. Both GLP-1 agonists and SGLT2 inhibitors consistently demonstrate renal benefits. Further studies of these new agents in different patient groups and in comparison to (or in combination with) other treatments are required to better define their role in combating the burden of diabetic kidney disease.
Insights
New diabetes drugs, including glucagon-like peptide 1 (GLP-1) agonists and sodium-glucose co-transporter 2 (SGLT2) inhibitors, show promise for preserving kidney function in patients with diabetic kidney disease.
Area of Science:
- Nephrology
- Endocrinology
- Pharmacology
Background:
- Diabetic kidney disease (DKD) poses a growing global health challenge.
- Effective therapies are needed to preserve renal function and prevent nephropathy.
- Recent advancements in hypoglycemic agents offer new therapeutic avenues.
Purpose of the Study:
- To review the impact of glycemic control on renal outcomes.
- To analyze clinical trial data for novel hypoglycemic drug classes.
- To evaluate the renal benefits of GLP-1 agonists, DPP-4 inhibitors, and SGLT2 inhibitors.
Main Methods:
- Systematic review of major clinical trials.
- Analysis of data on glycemic control and renal outcomes.
- Comparative assessment of different hypoglycemic agent classes.
Main Results:
- Glucagon-like peptide 1 (GLP-1) agonists demonstrate consistent renal benefits.
- Sodium-glucose co-transporter 2 (SGLT2) inhibitors consistently show renal benefits.
- Dipeptidyl peptidase-4 (DPP-4) inhibitors' renal impact requires further investigation.
Conclusions:
- GLP-1 agonists and SGLT2 inhibitors are valuable in managing diabetic kidney disease.
- Further research is needed to define optimal use in diverse patient populations.
- Combination therapies and comparative studies are essential to combat DKD burden.
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