Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Jul 21;17(7):943.
doi: 10.3390/pharmaceutics17070943.

Long-Term Effect of Semaglutide on the Glomerular Filtration Rate Slope in High-Risk Patients with Diabetic Nephropathy: Analysis in Real-World Clinical Practice

Affiliations

Long-Term Effect of Semaglutide on the Glomerular Filtration Rate Slope in High-Risk Patients with Diabetic Nephropathy: Analysis in Real-World Clinical Practice

Enrique Luna et al. Pharmaceutics. .

Abstract

Background: Semaglutide, a GLP-1 receptor agonist, has shown promising nephroprotective effects in clinical trials, though real-world data on its long-term impact on renal function in high-risk diabetic nephropathy patients remain scarce. Methods: We conducted a multicenter, retrospective observational study involving 156 patients with type 2 diabetes and chronic kidney disease (CKD) treated with subcutaneous semaglutide between 2019 and 2023. Inclusion required an eGFR > 15 mL/min/1.73 m2 or albuminuria > 30 mg/g and at least two years of follow-up. The primary outcome was the change in eGFR slope after semaglutide initiation. Subgroup analyses were performed based on baseline eGFR, albuminuria, and SGLT2i co-treatment. Results: In the whole study population, the median eGFR slope significantly improved from -3.29 (IQR 7.54) to -0.79 (IQR 6.01) mL/min/1.73 m2/year post-treatment (p < 0.001). Multiple linear regression showed a hazard ratio for the effect of semaglutide on the eGFR slope of 4.06 (2.43-5.68), p < 0.001. In patients with baseline eGFR < 60 mL/min/1.73 m2, the slope improved from -3.77 to -1.01 (p < 0.0001), while patients on concurrent SGLT2i therapy saw slope changes from -2.96 to -0.37 (p < 0.0001). Patients with albuminuria 30-1000 mg/g also improved from -2.96 to -0.04 (p < 0.0001); however, those > 1000 mg/g did not show a significant change (p = 0.184). Semaglutide also reduced BMI (p = 0.04), HbA1c (p = 0.002), triglycerides (p = 0.001), CRP (p = 0.003), and GGT values (p = 0.004). Conclusions: In real-world practice, semaglutide significantly attenuated renal function decline in high-risk diabetic patients, particularly those with advanced CKD or concurrent SGLT2i therapy. These findings support its nephroprotective role beyond glycemic control.

Keywords: SGLT2 inhibitors; chronic kidney disease; diabetes; eGFR slope; estimated glomerular filtration rate; semaglutide.

PubMed Disclaimer

Conflict of interest statement

Author Enrique Luna has received speaker honoraria and financial support for attending symposia from Novo Nordisk, Lilly, GSK and Esteve. The other authors declare that they have no conflict of interest. The companies had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Figures

Figure 1
Figure 1
Estimated glomerular filtration rate (eGFR) values of all patients before (A) and after (B) starting semaglutide treatment. Trend line with 95% confidence interval is shown.
Figure 2
Figure 2
Estimated glomerular filtration rate (eGFR) values before (A) and after (B) treatment with semaglutide in patients with eGFR < 60 L/min/1.73 m2. Trend line with 95% confidence interval is shown.
Figure 3
Figure 3
Mean values of estimated glomerular filtration rate (eGFR) slopes before and after treatment with semaglutide in patients who were already using SGLT2i (A) and in those who were not (B). ** p = 0.01, *** p < 0.0001.
Figure 4
Figure 4
Impact of semaglutide on the estimated glomerular filtration rate (eGFR) slope in patients with urinary albumin-to creatinine ratio (UACR) = 30–1000 mg/g (A) and patients with UACR > 1000 mg/g (B). Mean values are shown. *** p < 0.0001; ns, not significant.
Figure 5
Figure 5
Synergistic nephroprotective mechanism of GLP-1 RA and SGLT2i. Red lines denote inhibition. RAAS, Renin–Angiotensin–Aldosterone system; AGEs, advanced glycation end products; ROS, reactive oxygen species; REN, renin; AGII, angiotensin II; TFG-B1, transforming growth factor B1; TNF, tumor necrosis factor; NK-kB, nuclear factor kappa B; eGFR, estimated glomerular filtration rate; CKD, chronic kidney disease.

Similar articles

References

    1. Currie G., McKay G., Delles C. Biomarkers in diabetic nephropathy: Present and future. World J. Diabetes. 2014;5:763–776. doi: 10.4239/wjd.v5.i6.763. - DOI - PMC - PubMed
    1. Lewis E.J., Hunsicker L.G., Clarke W.R., Berl T., Pohl M.A., Lewis J.B., Ritz E., Atkins R.C., Rohde R., Raz I., et al. Renoprotective effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy due to type 2 diabetes. N. Engl. J. Med. 2001;345:851–860. doi: 10.1056/NEJMoa011303. - DOI - PubMed
    1. Heerspink H.J.L., Jongs N., Chertow G.M., Langkilde A.M., McMurray J.J.V., Correa-Rotter R., Rossing P., Sjöström C.D., Stefansson B.V., Toto R.D., et al. Effect of dapagliflozin on the rate of decline in kidney function in patients with chronic kidney disease with and without type 2 diabetes: A prespecified analysis from the DAPA-CKD trial. Lancet Diabetes Endocrinol. 2021;9:743–754. doi: 10.1016/S2213-8587(21)00242-4. - DOI - PubMed
    1. Li X., Song Y., Guo T., Xiao G., Li Q. Effect of glucagon-like peptide 1 receptor agonists on the renal protection in patients with type 2 diabetes: A systematic review and meta-analysis. Diabetes Metab. 2022;48:101366. doi: 10.1016/j.diabet.2022.101366. - DOI - PubMed
    1. Chen T.K., Sperati C.J., Thavarajah S., Grams M.E. Reducing Kidney Function Decline in Patients with CKD: Core Curriculum 2021. Am. J. Kidney Dis. 2021;77:969–983. doi: 10.1053/j.ajkd.2020.12.022. - DOI - PMC - PubMed

LinkOut - more resources