Key result
GLP-1 RAs and DPP-4 inhibitors show potential cardiorenal benefits in diabetic nephropathy.
Although there have been major advances in the understanding of the molecular mechanisms that contribute to the development of diabetic nephropathy, current best practice still leaves a significant treatment gap. The incidence of diabetes and associated nephropathy is increasing, with the main cause of mortality being related to cardiovascular causes. Novel therapies which are both 'cardio-renal'-protective seem the logical way forward. In the present review, we discuss the GLP-1 (glucagon-like peptide-1) receptor agonists and DPP-4 (dipeptidyl peptidase-4) inhibitors (incretin-based therapies), which are novel antidiabetic agents used in clinical practice and their role in diabetic nephropathy with specific focus on renoprotection and surrogate markers of cardiovascular disease. We discuss the pleiotropic effects of the incretin-based therapies apart from glucose-lowering and highlight the non-GLP-1 effects of DPP (dipeptidyl peptidase) inhibition. Large-scale clinical studies with cardiovascular end points are underway; however, studies with renal end points are lacking but much needed.
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Panchapakesan et al. (2012) conducted a review in Diabetic nephropathy and cardiovascular disease. GLP-1 receptor agonists and DPP-4 inhibitors was evaluated. GLP-1 receptor agonists and DPP-4 inhibitors show potential pleiotropic renoprotective and cardiovascular effects in diabetic nephropathy, though clinical trials with renal endpoints are lacking.
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