Department for Endocrinology and Diabetology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Division of Internal Medicine, Department of Gastroenterology and Diabetology, Community Hospital Bonn, Bonn, Germany.
Sci Rep. 2020 Dec 28;10(1):22396. doi: 10.1038/s41598-020-78734-z.
Recent studies have shown that high-risk patients with type 2 diabetes mellitus (T2DM) treated with sodium glucose cotransporter 2 (SGLT2) inhibitors have improved cardiovascular (CV) outcomes. In an exploratory analysis of data from the EMPA-REG study, elevations in haematocrit were shown to be strongly associated with beneficial CV effects. As insulin treatment has been shown to be antinatriuretic, with an associated increase in extracellular fluid volume, it is important to confirm whether haematocrit increase is maintained with concomitant insulin therapy. Here, we investigate the effect of the SGLT2 inhibitor dapagliflozin on haematocrit, red blood cell (RBC) counts and reticulocyte levels in high-risk patients with T2DM receiving insulin. A 24-week, double-blinded, randomised, placebo-controlled trial (ClinicalTrials.gov: NCT00673231) was reported previously with extension periods of 24 and 56 weeks (total of 104 weeks). Patients receiving insulin were randomised 1:1:1:1 to placebo or dapagliflozin at 2.5, 5 or 10 mg. Haematocrit, RBC and reticulocyte measurements were conducted during this study, and a longitudinal repeated-measures analysis was performed here to examine change from baseline during treatment. Dapagliflozin treatment in combination with insulin resulted in a dose-dependent increase in haematocrit levels and RBCs over a 104 week period. There was a short-term increase in reticulocyte levels at the start of treatment, which dropped to below baseline after 8 weeks. SGLT2 inhibition with dapagliflozin leads to a sustained increase in haematocrit in patients receiving chronic insulin treatment.
最近的研究表明,接受钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂治疗的 2 型糖尿病(T2DM)高危患者心血管(CV)结局得到改善。在 EMPA-REG 研究数据的探索性分析中,发现红细胞比容升高与 CV 有益效应密切相关。由于胰岛素治疗具有抗利钠作用,会伴随细胞外液容量增加,因此重要的是要确认在同时接受胰岛素治疗时,红细胞比容增加是否得以维持。在这里,我们研究 SGLT2 抑制剂达格列净对接受胰岛素治疗的 T2DM 高危患者的红细胞比容、红细胞计数和网织红细胞水平的影响。一项 24 周、双盲、随机、安慰剂对照试验(ClinicalTrials.gov:NCT00673231)先前已有报道,并延长了 24 周和 56 周(共 104 周)的扩展期。接受胰岛素治疗的患者按 1:1:1:1 的比例随机分为安慰剂或达格列净 2.5、5 或 10mg 组。在这项研究中进行了红细胞比容、红细胞和网织红细胞测量,并进行了纵向重复测量分析,以检查治疗期间从基线的变化。达格列净与胰岛素联合治疗在 104 周期间可使红细胞比容和红细胞水平呈剂量依赖性升高。治疗开始时网织红细胞水平短暂升高,8 周后降至低于基线。达格列净抑制 SGLT2 可使接受慢性胰岛素治疗的患者的红细胞比容持续升高。