钠-葡萄糖共转运蛋白-2抑制剂和胰高血糖素样肽-1受体激动剂对糖尿病患者蛋白尿和体重的影响

IF 4.6 3区 医学 Q1 ENDOCRINOLOGY & METABOLISM World Journal of Diabetes Pub Date : 2025-02-15 DOI:10.4239/wjd.v16.i2.98552
Di-Fei Lu, Rui Zheng, Ang Li, Jun-Qing Zhang
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引用次数: 0

摘要

背景:随着越来越多的证据显示对肾脏和心血管系统有益,糖尿病指南推荐糖尿病和慢性肾脏疾病(CKD)患者使用钠-葡萄糖共转运蛋白-2抑制剂(SGLT2i)和/或胰高血糖素样肽-1受体激动剂(GLP-1RAs)治疗肾脏保护。这两种药物对尿白蛋白-肌酐比(UACR)和肾小球滤过率(eGFR)的实际疗效仍有待探索。目的:评估现实世界糖尿病患者干预后SGLT2i和GLP-1RA的应用率和UACR改变。方法:选取北京大学第一医院糖尿病综合诊疗门诊5482例2型糖尿病患者为研究对象,随访至少6个月。进行倾向评分匹配,不推荐GLP-1RA或SGLT2i但性别类别和年龄相似的患者按1:2的比例分配到对照组。在现实世界的临床实践中,治疗6个月后评估血糖、体重、UACR和eGFR。结果:共有139例(2.54%)患者开始GLP-1RA治疗,387例(7.06%)患者接受SGLT2i治疗。6个月后,GLP-1RA组与SGLT2i组及对照组空腹血糖、餐后血糖、糖化血红蛋白的变化无显著差异。与对照组相比,UACR有更大的降低趋势,但差异无统计学意义(GLP-1RA与对照组相比,-2.20 vs 30.16 mg/g, P = 0.812;SGLT2i vs对照组,-20.61 vs 12.01 mg/g, P = 0.327);eGFR的改变也无显著差异。与对照组相比,GLP-1RA组体重明显减轻(GLP-1RA vs对照组,-0.90 vs 0.27 kg, P < 0.001), SGLT2i组(SGLT2i vs对照组,-0.59 vs -0.03 kg, P = 0.010)。结论:与接受其他降糖药物治疗的患者相比,接受SGLT2i或GLP-1RAs治疗的患者体重明显减轻,UACR呈下降趋势,并且在现实环境中具有相当的降糖效果。
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Efficacy of sodium-glucose cotransporter-2 inhibitors and glucagon-like peptide-1 receptor agonists on proteinuria and weight in a diabetes cohort.

Background: With accumulating evidence showing a benefit in the renal and cardiovascular systems, diabetes guidelines recommend that patients with diabetes and chronic kidney disease (CKD) be treated with sodium-glucose cotransporter-2 inhibitor (SGLT2i) and/or glucagon like peptide-1 receptor agonists (GLP-1RAs) for renal protection. The real-world efficacy of the two medications on the urinary albumin-creatinine ratio (UACR) and estimated glomerular filtration rate (eGFR) remains to be explored.

Aim: To evaluate the SGLT2i and GLP-1RA application rates and UACR alterations after intervention in a real-world cohort of patients with diabetes.

Methods: A cohort of 5482 patients with type 2 diabetes were enrolled and followed up at the Integrated Care Clinic for Diabetes of Peking University First Hospital for at least 6 months. Propensity score matching was performed, and patients who were not recommended for GLP-1RA or SGLT2i with comparable sex categories and ages were assigned to the control group at a 1:2 ratio. Blood glucose, body weight, UACR and eGFR were evaluated after 6 months of treatment in real-world clinical practice.

Results: A total of 139 (2.54%) patients started GLP-1RA, and 387 (7.06%) received SGLT2i. After 6 months, the variations in fasting blood glucose, prandial blood glucose, and glycosylated hemoglobin between the GLP-1RA group and the SGLT2i and control groups were not significantly different. UACR showed a tendency toward a greater reduction compared with the control group, although this difference was not statistically significant (GLP-1RA vs control, -2.20 vs 30.16 mg/g, P = 0.812; SGLT2i vs control, -20.61 vs 12.01 mg/g, P = 0.327); eGFR alteration also showed no significant differences. Significant weight loss was observed in the GLP-1RA group compared with the control group (GLP-1RA vs control, -0.90 vs 0.27 kg, P < 0.001), as well as in the SGLT2i group (SGLT2i vs control, -0.59 vs -0.03 kg, P = 0.010).

Conclusion: Compared with patients who received other glucose-lowering drugs, patients receiving SGLT2i or GLP-1RAs presented significant weight loss, a decreasing trend in UACR and comparable glucose-lowering effects in real-world settings.

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来源期刊
World Journal of Diabetes
World Journal of Diabetes ENDOCRINOLOGY & METABOLISM-
自引率
2.40%
发文量
909
期刊介绍: The WJD is a high-quality, peer reviewed, open-access journal. The primary task of WJD is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of diabetes. In order to promote productive academic communication, the peer review process for the WJD is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJD are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in diabetes. Scope: Diabetes Complications, Experimental Diabetes Mellitus, Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus, Diabetes, Gestational, Diabetic Angiopathies, Diabetic Cardiomyopathies, Diabetic Coma, Diabetic Ketoacidosis, Diabetic Nephropathies, Diabetic Neuropathies, Donohue Syndrome, Fetal Macrosomia, and Prediabetic State.
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