Department of Endocrinology, First Hospital of Shanxi Medical University, Taiyuan, China; First Clinical Medical College, Shanxi Medical University, Taiyuan, China.
The Third Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Taiyuan, 030032, China.
J Diabetes Complications. 2023 Dec;37(12):108632. doi: 10.1016/j.jdiacomp.2023.108632. Epub 2023 Oct 21.
Patients undergoing insulin-based therapy for type 1 diabetes often experience poor glycemic control characterized by significant fluctuations. This study was undertaken to analyze the effect of sodium-glucose cotransporter 2 inhibitors (SGLT2Is), as an adjunct to insulin, on time in range (TIR) and glycemic variability in patients with type 1 diabetes, using continuous glucose monitoring (CGM). In addition, we examined which type of SGLT2I yielded a superior effect compared to others.
We conducted a comprehensive search of PubMed, EMBASE, the Cochrane Library, Web of Science, and clinical trial registry websites, retrieving all eligible randomized clinical trials (RCTs) published up until February 2023. We analyzed the mean TIR, mean amplitude of glucose excursions (MAGE), mean daily glucose (MDG), diabetic ketoacidosis (DKA), standard deviation (SD), total insulin dose, and severe hypoglycemia to evaluate the efficacy and safety of SGLT2Is. A random-effects model was also employed.
This study encompassed 15 RCTs. The meta-analysis revealed that the use of SGLT2Is as an adjuvant therapy to insulin led to a significant increase in TIR (MD = 10.78, 95%CI = 9.33-12.23, I = 42 %, P < 0.00001) and a decrease in SD (MD = -0.38, 95%CI = -0.50 to -0.26, I = 0 %, P < 0.00001), MAGE (MD = -0.92, 95%CI = -1.17 to -0.67, I = 19 %, P < 0.00001), MDG(MD = -1.01, 95%CI = -1.32 to -0.70, I = 48 %, P < 0.00001), and total insulin dose (MD = -5.81, 95%CI = -7.81 to -3.82, I = 32 %, P < 0.00001). No significant increase was observed in the rate of severe hypoglycemia (RR = 1.04, 95 % CI = 0.76-1.43, P = 0.80). However, SGLT2I therapy was associated with increased DKA occurrence (RR = 2.79, 95 % CI = 1.42-5.48; P = 0.003, I = 16 %). In addition, the subgroup analyses based on the type of SGLT2Is revealed that dapagliflozin might exhibit greater efficacy compared to other SGLT2Is across most outcomes.
SGLT2Is exhibited a positive effect on improving blood glucose level fluctuations. Subgroup analysis showed that dapagliflozin appeared to have more advantages. However, giving due consideration to preventing adverse effects, particularly DKA, is paramount.
Prospero CRD42023408276.
接受胰岛素治疗的 1 型糖尿病患者常出现血糖控制不佳,表现为明显波动。本研究旨在通过连续血糖监测(CGM)分析钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)作为胰岛素辅助治疗对 1 型糖尿病患者时间在目标范围内(TIR)和血糖变异性的影响。此外,我们还研究了哪种 SGLT2i 比其他类型的药物效果更好。
我们对 PubMed、EMBASE、Cochrane 图书馆、Web of Science 和临床试验注册网站进行了全面检索,检索截至 2023 年 2 月发表的所有符合条件的随机对照临床试验(RCT)。我们分析了 TIR、平均血糖波动幅度(MAGE)、平均每日血糖(MDG)、糖尿病酮症酸中毒(DKA)、标准差(SD)、总胰岛素剂量和严重低血糖的变化,以评估 SGLT2i 的疗效和安全性。还使用了随机效应模型。
本研究共纳入 15 项 RCT。Meta 分析结果显示,SGLT2i 作为胰岛素的辅助治疗可显著增加 TIR(MD=10.78,95%CI=9.33-12.23,I²=42%,P<0.00001)和降低 SD(MD=-0.38,95%CI=-0.50 至-0.26,I²=0%,P<0.00001)、MAGE(MD=-0.92,95%CI=-1.17 至-0.67,I²=19%,P<0.00001)、MDG(MD=-1.01,95%CI=-1.32 至-0.70,I²=48%,P<0.00001)和总胰岛素剂量(MD=-5.81,95%CI=-7.81 至-3.82,I²=32%,P<0.00001)。严重低血糖的发生率无显著增加(RR=1.04,95%CI=0.76-1.43,P=0.80)。然而,SGLT2i 治疗与 DKA 发生率增加相关(RR=2.79,95%CI=1.42-5.48;P=0.003,I²=16%)。此外,基于 SGLT2i 类型的亚组分析显示,达格列净在大多数结局上可能比其他 SGLT2i 更有效。
SGLT2i 对改善血糖波动水平有积极作用。亚组分析表明,达格列净似乎具有更多优势。然而,在考虑预防不良反应,特别是 DKA 时,必须谨慎权衡。
PROSPERO CRD42023408276。