# Effect of Ozempic on Diabetic Nephropathy: A Case Report

**Authors:** Jimmy Joseph

PMC · DOI: 10.7759/cureus.87416 · Cureus · 2025-07-07

## TL;DR

A 40-year-old man with type 2 diabetes and kidney issues saw significant improvements in blood sugar and kidney function after using Ozempic.

## Contribution

This case report demonstrates the renoprotective and metabolic benefits of semaglutide in a patient intolerant to SGLT2 inhibitors.

## Key findings

- HbA1c decreased from 9.8% to 6.1% over 12 months with semaglutide therapy.
- Urine albumin-to-creatinine ratio dropped from 267 mg/g to 34 mg/g, indicating improved kidney function.
- eGFR improved, suggesting a positive impact on renal function.

## Abstract

Semaglutide (Ozempic), a Glucagon-like peptide-1 (GLP-1) receptor agonist, has shown promise in improving glycemic control and offering renal protection in type 2 diabetes. We present the case of a 40-year-old male with poorly controlled type 2 diabetes and early diabetic nephropathy, who experienced significant metabolic and renal improvements following semaglutide therapy. Initially, on SGLT2 inhibitors, the patient discontinued treatment due to recurrent urinary tract infections. On presentation, he exhibited hyperglycemia, dyslipidemia, proteinuria, and reduced eGFR. Semaglutide was initiated alongside metformin, gliclazide, antihypertensives, and lipid-lowering agents. Over 12 months, HbA1c improved from 9.8% to 6.1%, and urine albumin-to-creatinine ratio decreased from 267 mg/g to 34 mg/g, with improved eGFR. This case supports the renoprotective and metabolic benefits of semaglutide and highlights its potential as a therapeutic option in patients intolerant to SGLT2 inhibitors.

## Linked entities

- **Chemicals:** semaglutide (PubChem CID 56843331), metformin (PubChem CID 4091), gliclazide (PubChem CID 3475)
- **Diseases:** type 2 diabetes (MONDO:0005148), diabetic nephropathy (MONDO:0005016), hyperglycemia (MONDO:0002909), dyslipidemia (MONDO:0002525), proteinuria (MONDO:0003634)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** hyperglycemia (MESH:D006943), dyslipidemia (MESH:D050171), Diabetic Nephropathy (MESH:D003928), proteinuria (MESH:D011507), urinary tract infections (MESH:D014552), type 2 diabetes (MESH:D003924)
- **Chemicals:** gliclazide (MESH:D005907), metformin (MESH:D008687), creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12326341/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12326341/full.md

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Source: https://tomesphere.com/paper/PMC12326341