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Endocrine Abstracts (2025) 110 EP558 | DOI: 10.1530/endoabs.110.EP558

1University of Sousse, Faculty of Medicine of Sousse, Farhat Hached University Hospital, Endocrinology Diabetology Department, 4000, Sousse, Tunisia, Sousse, Tunisia; 2University of Sousse, Faculty of Medicine of Sousse, Farhat Hached University Hospital, Biochemistry Department, 4000, Sousse, Tunisia, Sousse, Tunisia


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Background: SGLT2-inhibitors have revolutionized the management of type 2 diabetes mellitus by promoting urinary glucose excretion, thereby reducing blood glucose levels. Beyond their role in diabetes management, these agents have shown promise in mitigating cardiovascular and renal complications. This study aimed to evaluate the effects of SGLT2-inhibitors on glycemic control, renal function, and metabolic parameters in patients with diabetes.

Methods: A descriptive retrospective study was conducted at the Endocrinology Department of Farhat-Hached University Hospital in Sousse, Tunisia. The study included diabetic patients evaluated over two periods: P1 from January to March 2024 and P2 from March to June 2024. They were divided into two groups: those receiving SGLT2-inhibitor treatment in P2 (G1) and a control group (G2). All patients underwent fasting blood glucose (FBG), glycated hemoglobin (A1c), lipid profile, renal assessment, and microalbuminuria testing.

Results: A total of 72 patients were evaluated. G1 included 36 patients, and G2 also consisted of 36 patients. The mean age of participants was 64±9.26 years in G1 and 62±8.64 years in G2, with no significant difference (P = 0.36). Both groups had a female predominance (55.5%). Chronic imbalance of diabetes under insulin was the most common reason for admission (52.8%). During P1, no significant differences were observed in A1c, FBG, creatinine, or microalbuminuria between the groups. However, during P2, G1 demonstrated significantly lower A1c (9.07%±1.82% vs. 10.16%±1.40%, P = 0.007) and FBG levels (1.51±0.57 g/l vs. 2.36±0.80 g/l, P<10-3) compared to G2. Microalbuminuria was also significantly reduced in G1 (65±111.18 mg/24h vs. 492±1137.80 mg/24h, P = 0.032). No significant differences were noted in lipid profiles or creatinine levels between the groups.

Conclusion: SGLT2-inhibitors significantly improved glycemic control and reduced microalbuminuria in diabetic patients, highlighting their potential to slow the progression of chronic kidney disease (CKD). Their efficacy and safety across CKD stages 1 to 4 position them as a promising therapeutic option for managing diabetes and its renal complications.

Volume 110

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course

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