# Efficacy and safety of sodium-glucose cotransporter 2 inhibitors in the treatment of diabetic kidney disease: a meta-analysis

**Authors:** Yingbo Guo, Wenfeng Gao, Shichao Li, Xiaona An, Zhongjie Liu

PMC · DOI: 10.3389/fendo.2025.1596888 · Frontiers in Endocrinology · 2026-01-27

## TL;DR

This study finds that SGLT2 inhibitors help improve kidney function in diabetic patients but increase the risk of genital infections and diabetic ketoacidosis.

## Contribution

A meta-analysis confirming the efficacy and safety profile of SGLT2 inhibitors in diabetic kidney disease patients.

## Key findings

- SGLT2 inhibitors significantly reduce glomerular filtration rate decline and blood pressure in diabetic kidney disease patients.
- The treatment is associated with a higher risk of genital infections and diabetic ketoacidosis.
- No significant difference in overall adverse events, urinary tract infections, bone fractures, or hypoglycemia was observed.

## Abstract

Diabetic kidney disease is a major cause of end-stage renal disease. Herein, we aimed to assess the efficacy and safety of sodium-glucose cotransporter 2 (SGLT2) inhibitors in patients with diabetic kidney disease.

PubMed, Embase, and Web of Science databases were searched for eligible randomized clinical trials (RCTs) published up to July 2024. Effect sizes were summarized as risk ratios (RR) or weighted mean differences (WMD) with 95% confidence intervals (CI). Statistical analyses were performed using Stata.

Fifteen studies (24463 patients) were included in the meta-analysis. The results of the meta-analysis showed that compared with the control group, SGLT2 inhibitor intervention could reduce the estimated glomerular filtration rate (WMD=−2.47; 95% CI: −3.18, −1.76), systolic blood pressure (WMD=−4.09; 95% CI: −4.97 to -3.21), diastolic blood pressure (WMD=−2.47; 95% CI: −3.06 to −1.88), and glycated hemoglobin (WMD=−0.27; 95% CI: −0.38, −0.17). Moreover, there was no significant difference between the SGLT2 inhibitor and control groups in terms of the incidence of overall adverse event, urinary tract infection, bone fracture and hypoglycemia. However, the incidence of genital infection and diabetic ketoacidosis in the SGLT2 inhibitor group was higher than that in the control group.

Our study confirms the beneficial effects in diabetic kidney disease patients, while also demonstrating a higher risk of genital infections and diabetic ketoacidosis in the SGLT2 inhibitor group compared to controls.

## Linked entities

- **Diseases:** diabetic kidney disease (MONDO:0005016), end-stage renal disease (MONDO:0004375), diabetic ketoacidosis (MONDO:0012819)

## Full-text entities

- **Genes:** SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}
- **Diseases:** bone fracture (MESH:D050723), end-stage renal disease (MESH:D007676), diabetic ketoacidosis (MESH:D016883), hypoglycemia (MESH:D007003), Diabetic kidney disease (MESH:D003928), urinary tract infection (MESH:D014552), genital infection (MESH:D007239)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12886043/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12886043/full.md

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Source: https://tomesphere.com/paper/PMC12886043