Division of Endocrinology and Metabolism, Department of Internal Medicine, Cerrahpasa Medical School, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Department of Histology and Embryology, Cerrahpasa Medical School, Istanbul University-Cerrahpasa, Istanbul, Turkey.
J Diabetes. 2022 Apr;14(4):236-246. doi: 10.1111/1753-0407.13261. Epub 2022 Feb 28.
The aim of this study was to investigate the effects of sodium glucose cotransporter 2 inhibitors (SGLT2i) on the glomerulus through the evaluation of podocyturia in patients with diabetic kidney disease (DKD).
The study population was composed of 40 male patients with type 2 diabetes mellitus; 22 of them received SGLT2i (SGLT2i group), and the others who did not were the control. The DKD-related parameters of patients were monitored before SGLT2i initiation, and then in the third and sixth month of the follow-up period. Patients' demographic, clinical, laboratory, and follow-up data were obtained from medical charts. Microalbuminuria was measured in 24-h urine. The number of podocytes in the urine was determined by immunocytochemical staining of two different markers, namely podocalyxin (podx) and synaptopodin (synpo). Concentrations of urine stromal cell-derived factor 1a and vascular endothelial growth factor cytokines were quantified with an enzyme-linked immunosorbent assay kit.
At the end of the follow-up period, decreases in glycosylated hemoglobin, glucose, systolic and diastolic blood pressure, uric acid level, and microalbuminuria, and improvement in body mass index level and weight loss were significant for the SGLT2i group. On the other hand, there was no significant difference in terms of these parameters in the control group. The excretion of synaptopodin-positive (synpo ) and podocalyxin-positive (podx ) cells was significantly reduced at the end of the follow-up period for the SGLT2i group, while there was no significant change for the control.
At the end of the follow-up period, male patients receiving SGLT2i had better DKD-related parameters and podocyturia levels compared to baseline and the control group. Our data support the notion that SGLT2i might have structural benefits for glomerular health.
本研究旨在通过评估糖尿病肾病(DKD)患者的足细胞尿,来研究钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)对肾小球的影响。
研究人群由 40 名男性 2 型糖尿病患者组成;其中 22 名接受 SGLT2i(SGLT2i 组)治疗,其余未接受 SGLT2i 治疗的患者作为对照组。在开始 SGLT2i 治疗前以及随访的第 3 个月和第 6 个月监测患者的 DKD 相关参数。从病历中获取患者的人口统计学、临床、实验室和随访数据。通过 24 小时尿液测量微量白蛋白尿。通过免疫细胞化学染色两种不同的标志物,即足突蛋白(podx)和突触蛋白(synpo),来确定尿中足细胞的数量。使用酶联免疫吸附试验试剂盒定量测定尿基质细胞衍生因子 1a 和血管内皮生长因子细胞因子的浓度。
随访期末,SGLT2i 组患者的糖化血红蛋白、血糖、收缩压和舒张压、尿酸水平和微量白蛋白尿降低,体重指数水平和体重减轻改善,差异有统计学意义。另一方面,对照组这些参数无显著差异。随访期末,SGLT2i 组 synaptopodin 阳性(synpo)和 podocalyxin 阳性(podx)细胞的排泄明显减少,而对照组无明显变化。
随访期末,与基线和对照组相比,接受 SGLT2i 治疗的男性患者 DKD 相关参数和足细胞尿水平更好。我们的数据支持 SGLT2i 可能对肾小球健康具有结构益处的观点。