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The nephrological perspective on SGLT-2 inhibitors in type 1 diabetes
Pieter Gillard1, Oliver Schnell2, Per-Henrik Groop3
1Department of Endocrinology, University Hospitals Leuven, KU Leuven, Belgium.
Abstract:
Prevalence of type 1 diabetes mellitus (T1DM) is globally continuously increasing. T1DM is accompanied by a high risk of developing cardiovascular and renal comorbidities and is one of the leading causes of end-stage renal disease (ESRD). However, current therapeutic approaches for chronic and/or diabetic kidney disease (CKD/DKD) existed for a long time, and offer room for improvement, particularly in T1DM. In 2019, the European Medicines Agency (EMA) approved a first sodium/glucose co-transporter 2 inhibitor (SGLT-2i) and a first dual SGLT-1/-2i to improve glycaemic control, as an adjunctive treatment to insulin in persons with T1DM and a body mass index ≥27 kg/m2. Of note, SGLT-1/2is and SGLT-2is are not approved by the Food and Drug Administration (FDA) as an adjunct treatment in T1DM, nor approved for the treatment of CKD or DKD by EMA and FDA. SGLT is have shown to mediate different renoprotective effects in type 2 diabetes mellitus in corresponding cardiovascular and renal outcome trials. First efficacy trials offer insights into potential positive effects on renal function and kidney disease of SGLTis in T1DM. This review summarizes and discusses latest available data on SGLT inhibition and provides an update on the nephrological perspective on SGLTis, specifically in T1DM.
Insights
Sodium-glucose co-transporter inhibitors (SGLT-Is) show promise for managing type 1 diabetes mellitus (T1DM) and its associated kidney disease. Emerging data suggests potential renoprotective effects, offering new therapeutic avenues.
Area of Science:
- Nephrology
- Endocrinology
- Pharmacology
Background:
- Type 1 diabetes mellitus (T1DM) prevalence is rising globally, increasing the risk of cardiovascular and renal comorbidities, including end-stage renal disease (ESRD).
- Existing treatments for chronic and/or diabetic kidney disease (CKD/DKD) in T1DM patients require improvement.
- Sodium-glucose co-transporter inhibitors (SGLT-Is), including dual SGLT-1/-2 inhibitors, were approved in 2019 by the EMA for glycemic control in T1DM with obesity, but lack FDA approval for T1DM or kidney disease treatment.
Purpose of the Study:
- To review and discuss the latest data on SGLT inhibition in T1DM.
- To provide an update on the nephrological perspective of SGLT inhibitors in T1DM.
- To explore the potential renoprotective effects of SGLT inhibitors in T1DM.
Main Methods:
- Literature review of recent clinical trials and studies on SGLT inhibitors in T1DM.
- Analysis of data from cardiovascular and renal outcome trials involving SGLT inhibitors in type 2 diabetes mellitus.
- Synthesis of nephrological insights regarding SGLT inhibition in T1DM.
Main Results:
- SGLT inhibitors have demonstrated renoprotective effects in type 2 diabetes mellitus.
- Initial efficacy trials indicate potential benefits of SGLT inhibitors on renal function and kidney disease in T1DM.
- SGLT-1/-2 inhibitors and SGLT-2 inhibitors are approved by EMA for glycemic control in T1DM with obesity, but not by FDA for T1DM or kidney disease.
Conclusions:
- SGLT inhibitors represent a promising therapeutic strategy for managing T1DM and its associated kidney complications.
- Further research and clinical trials are warranted to fully elucidate the role of SGLT inhibitors in T1DM nephropathy.
- The nephrological perspective highlights the potential of SGLT inhibition to improve renal outcomes in T1DM patients.
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