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Sodium-Glucose Cotransporter-2 Inhibitors Could Help Delay Renal Impairment in Patients with Type 2 Diabetes: A
Gyunam Park1, Byungha Choi1,2, Soyoung Kang1,3
1Department of Pharmacy and Yonsei Institute of Pharmaceutical Sciences, Yonsei University, Incheon 21983, Korea.
Abstract:
This study compared the renoprotective effects of sodium−glucose cotransporter-2 (SGLT2) inhibitors and dipeptidyl peptidase-4 (DPP-4) inhibitors in patients with type 2 diabetes mellitus (T2DM). We performed a retrospective cohort study using electronic medical records of patients with T2DM. The primary outcome was the first occurrence of an estimated glomerular filtration rate (eGFR) <45 mL/min/1.73 m2 after the index date. We analyzed changes in repeatedly measured laboratory data, such as eGFR and serum uric acid (SUA). We included 2396 patients (1198 patients in each group) in the present study. The rate of renal events was significantly lower in the SGLT2 inhibitors group than that in the DPP-4 inhibitors group (hazard ratio, 0.46; 95% CI, 0.29 to 0.72; p = 0.0007). The annual mean change in the eGFR was significantly smaller in the SGLT2 inhibitors group than that in the DPP-4 inhibitors group, with a between-group difference of 0.86 ± 0.18 mL/min/1.73 m2 per year (95% CI, 0.49 to 1.23; p < 0.0001). Moreover, the mean change in SUA was lower in the SGLT2 inhibitors group. Considering the lower incidence of renal impairment, the slower decline in eGFR, and reduced SUA, SGLT2 inhibitors could help delay renal impairment in patients with T2DM.
Insights
Sodium-glucose cotransporter-2 (SGLT2) inhibitors demonstrated superior renoprotective effects compared to dipeptidyl peptidase-4 (DPP-4) inhibitors in type 2 diabetes mellitus patients. SGLT2 inhibitors significantly reduced renal events and slowed estimated glomerular filtration rate decline.
Area of Science:
- Nephrology
- Endocrinology
- Pharmacology
Background:
- Type 2 diabetes mellitus (T2DM) is a leading cause of chronic kidney disease.
- Both sodium-glucose cotransporter-2 (SGLT2) inhibitors and dipeptidyl peptidase-4 (DPP-4) inhibitors are used to manage T2DM.
- Comparative data on their long-term renoprotective effects are crucial.
Purpose of the Study:
- To compare the renoprotective efficacy of SGLT2 inhibitors versus DPP-4 inhibitors in T2DM patients.
- To evaluate the impact of these drug classes on renal function decline and serum uric acid levels.
Main Methods:
- Retrospective cohort study utilizing electronic medical records.
- Inclusion of 2396 T2DM patients, with 1198 in each treatment group (SGLT2 inhibitors vs. DPP-4 inhibitors).
- Primary outcome: first occurrence of estimated glomerular filtration rate (eGFR) <45 mL/min/1.73 m2; secondary analysis of eGFR and serum uric acid (SUA) changes.
Main Results:
- Significantly lower rate of renal events in the SGLT2 inhibitors group (HR, 0.46; p = 0.0007).
- Slower annual mean eGFR decline in the SGLT2 inhibitors group (0.86 mL/min/1.73 m2/year; p < 0.0001).
- Lower mean serum uric acid levels observed with SGLT2 inhibitors.
Conclusions:
- SGLT2 inhibitors exhibit superior renoprotective properties compared to DPP-4 inhibitors in T2DM.
- These findings suggest SGLT2 inhibitors can delay the progression of renal impairment in T2DM patients.
- The reduction in eGFR decline and SUA levels highlights a potential mechanism for renoprotection.
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