Joseph Jimmy
Internal Medicine, Aster DM Healthcare, Dubai, ARE.
Cureus. 2025 Jul 7;17(7):e87416. doi: 10.7759/cureus.87416. eCollection 2025 Jul.
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.
司美格鲁肽(Ozempic)是一种胰高血糖素样肽-1(GLP-1)受体激动剂,已显示出在改善2型糖尿病患者血糖控制及提供肾脏保护方面的前景。我们报告一例40岁男性2型糖尿病控制不佳且患有早期糖尿病肾病患者,其在接受司美格鲁肽治疗后代谢及肾脏状况有显著改善。最初,该患者使用钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂时,因反复发生尿路感染而停药。初诊时,他表现为高血糖、血脂异常、蛋白尿及估算肾小球滤过率(eGFR)降低。遂开始使用司美格鲁肽,同时联用二甲双胍、格列齐特、抗高血压药及降脂药。在12个月的时间里,糖化血红蛋白(HbA1c)从9.8%降至6.1%,尿白蛋白与肌酐比值从267mg/g降至34mg/g,eGFR有所改善。该病例支持司美格鲁肽具有肾脏保护及代谢益处,并突出了其在不耐受SGLT2抑制剂的患者中作为一种治疗选择的潜力。