Wang Y, Xu L, Yuan L, Li D, Zhang Y, Zheng R, Liu C, Feng X, Li Q, Li Q, Ma J
Department of Endocrinology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Department of Medicine, Kunshan Rehabilitation Hospital, Suzhou, China.
Diabet Med. 2016 Dec;33(12):1732-1736. doi: 10.1111/dme.13107. Epub 2016 May 26.
To observe changes in atrial natriuretic peptide levels after treatment with sodium-glucose co-transporter-2 inhibitors in patients with newly diagnosed type 2 diabetes.
A total of 28 patients with newly diagnosed Type 2 diabetes and HbA levels of 58 -91 mmol/mol (7.5-10.5%) were randomly selected to receive sodium-glucose co-transporter-2 inhibitor treatment (n = 18) or placebo (n = 10) for 24 weeks. We analysed atrial natriuretic peptide concentrations, using an enzyme-linked immunosorbent assay. In addition, sodium and HbA levels were measured at baseline, 12 weeks and 24 weeks and blood lipid levels and insulin sensitivities at baseline and 24 weeks.
Compared with patients treated with placebo, patients who received sodium-glucose co-transporter-2 inhibitor treatment exhibited lower atrial natriuretic peptide levels (36.74 vs 56.90 pg/ml in the placebo group; P < 0.05) and higher sodium levels (144.3 vs 141.4 mmol/l in the placebo group; P < 0.01) at 24 weeks, after adjusting for baseline values. HbA levels were lower after sodium-glucose co-transporter-2 inhibitor treatment compared with placebo (51 vs 60 mmol/mol; P < 0.01). No correlation was found between atrial natriuretic peptide and HbA levels. Homeostatic model assessment of β-cell function values and lipid profiles were generally similar after 24 weeks of treatment with placebo or sodium-glucose co-transporter-2 inhibitor.
This study shows the ability of sodium-glucose co-transporter-2 inhibitors to lower atrial natriuretic peptide levels and improve glycaemic control, which may benefit the cardiovascular system.
观察钠-葡萄糖协同转运蛋白2抑制剂治疗新诊断2型糖尿病患者后心房利钠肽水平的变化。
随机选取28例新诊断的2型糖尿病患者,糖化血红蛋白(HbA)水平为58 - 91 mmol/mol(7.5 - 10.5%),接受钠-葡萄糖协同转运蛋白2抑制剂治疗(n = 18)或安慰剂治疗(n = 10),为期24周。我们采用酶联免疫吸附测定法分析心房利钠肽浓度。此外,在基线、12周和24周时测量钠和HbA水平,在基线和24周时测量血脂水平和胰岛素敏感性。
在调整基线值后,与接受安慰剂治疗的患者相比,接受钠-葡萄糖协同转运蛋白2抑制剂治疗的患者在24周时心房利钠肽水平较低(安慰剂组为56.90 pg/ml,治疗组为36.74 pg/ml;P < 0.05),钠水平较高(安慰剂组为141.4 mmol/l,治疗组为144.3 mmol/l;P < 0.01)。与安慰剂相比,钠-葡萄糖协同转运蛋白2抑制剂治疗后HbA水平较低(51 vs 60 mmol/mol;P < 0.01)。未发现心房利钠肽与HbA水平之间存在相关性。安慰剂或钠-葡萄糖协同转运蛋白2抑制剂治疗24周后,β细胞功能值和血脂谱的稳态模型评估总体相似。
本研究表明钠-葡萄糖协同转运蛋白2抑制剂能够降低心房利钠肽水平并改善血糖控制,这可能对心血管系统有益。