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GLP-1 Receptor Agonists and SGLT-2 Inhibitors in Diabetic Nephropathy: A Comparative Study
Sara Ghadeer Alghadeer1, Sama Sami Kanfar1, Zakiah Dheya Algallaf1
1Imam Abdulrahman bin Faisal, King Fahad University Hospital, Dammam, Kingdom of Saudi Arabia.
Objective:
To investigate the effects of glucagon-like peptide-1 receptor agonist (GLP-1RAs) on renal function in type 2 diabetes mellitus (T2DM) patients and compared their efficacy to sodium-glucose co-transporter-2 inhibitors (SGLT-2i) in managing diabetic nephropathy.
Methods:
This is a retrospective cohort study conducted at King Fahad University Hospital, including 115 adults (≥18 years) with T2DM and baseline estimated glomerular filtration rate (eGFR) ≥60 mL/min/1.73m2, treated with GLP-1RAs or SGLT-2i for over 1 year. Patients on renal replacement therapy, nephrotoxic drugs, or with incomplete records were excluded. Data were analyzed with Jeffrey's Amazing Statistics Program; the significant value is p < 0.05.
Results:
Participants were treated with either SGLT-2i (67.8%) or GLP-1RAs (32.2%). Both groups showed minimal improvements in glycemic control, hemoglobin A1c decreased from 7.86% to 7.66% (SGLT-2i) and from 8% to 7.76% (GLP-1RAs). Estimated GFR minimally improved by 0.5-1.2 mL/min/1.73m2 (GLP-1RAs) and changed by -1.2 to +10.1 mL/min/1.73m2 (SGLT-2i). Urine albumin/creatinine ratio dropped by 13.35 mg/g with GLP-1RAs but increased by 49.86 mg/g with SGLT-2i.
Conclusions:
Both medications offered comparable glycemic and renal benefits. The GLP-1RAs, however, demonstrated more favorable effects on albuminuria, suggesting potential for superior renal protection in nascent diabetic nephropathy.
Insights
Glucagon-like peptide-1 receptor agonists (GLP-1RAs) and sodium-glucose co-transporter-2 inhibitors (SGLT-2i) offer comparable benefits for type 2 diabetes mellitus (T2DM) patients. GLP-1RAs showed better reduction in albuminuria, indicating potential for superior kidney protection.
Area of Science:
- Nephrology
- Endocrinology
- Pharmacology
Background:
- Type 2 diabetes mellitus (T2DM) is a leading cause of chronic kidney disease.
- Diabetic nephropathy management requires effective glycemic control and renoprotective strategies.
- Glucagon-like peptide-1 receptor agonists (GLP-1RAs) and sodium-glucose co-transporter-2 inhibitors (SGLT-2i) are novel therapeutic classes for T2DM with potential renal benefits.
Purpose of the Study:
- To investigate the effects of GLP-1RAs on renal function in T2DM patients.
- To compare the efficacy of GLP-1RAs versus SGLT-2i in managing diabetic nephropathy.
- To evaluate the impact of these agents on estimated glomerular filtration rate (eGFR) and albuminuria.
Main Methods:
- Retrospective cohort study of 115 adult T2DM patients with eGFR ≥60 mL/min/1.73m².
- Patients were treated with either GLP-1RAs or SGLT-2i for over one year.
- Exclusion criteria included renal replacement therapy, nephrotoxic drugs, and incomplete records. Data analyzed using Jeffrey's Amazing Statistics Program (p < 0.05).
Main Results:
- Both GLP-1RAs and SGLT-2i groups showed minimal improvements in glycemic control (HbA1c).
- eGFR showed minimal improvement with GLP-1RAs (0.5-1.2 mL/min/1.73m²) and variable changes with SGLT-2i (-1.2 to +10.1 mL/min/1.73m²).
- Urine albumin/creatinine ratio decreased with GLP-1RAs (-13.35 mg/g) but increased with SGLT-2i (+49.86 mg/g).
Conclusions:
- GLP-1RAs and SGLT-2i provide comparable glycemic and renal benefits in T2DM patients.
- GLP-1RAs demonstrated a more favorable impact on reducing albuminuria.
- GLP-1RAs may offer superior renal protection in early-stage diabetic nephropathy.
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