Second Propedeutic Department of Internal Medicine, General Hospital "Hippokration", Aristotle University of Thessaloniki, Thessaloniki, Greece.
Second Propedeutic Department of Internal Medicine, General Hospital "Hippokration", Aristotle University of Thessaloniki, Thessaloniki, Greece.
Diabetes Res Clin Pract. 2019 Dec;158:107927. doi: 10.1016/j.diabres.2019.107927. Epub 2019 Nov 13.
Sodium-glucose co-transporter-2 inhibitors (SGLT-2i) and glucagon-like peptide-1 receptor agonists (GLP-1RAs) are now considered as key players in the treatment of type 2 diabetes mellitus (T2DM). The purpose of this meta-analysis was to provide precise effect estimates regarding the safety and efficacy of the addition of a GLP-1RA on top of SGLT-2i treatment.
PubMed and CENTRAL, along with grey literature sources, were searched from their inception to May 2019 for randomized controlled trials (RCTs) with a duration ≥ 12 weeks, evaluating the safety and efficacy of addition of a GLP-1RA on a SGLT-2i compared to SGLT-2i alone in patients with T2DM. We also used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach to assess the credibility of our summary estimates.
We identified three eligible RCTs, pooling data retrieved from 1,042 patients with T2DM in total. Administration of the maximum dose of a GLP-1RA on top of SGLT-2i treatment compared to SGLT-2i alone resulted in significant decrease in HbA1c by 0.91% (95% CI; -1.41 to -0.42) [GRADE: moderate], in body weight by 1.95 kg (95% CI; -3.83 to -0.07) [GRADE: moderate], in fasting plasma glucose by 1.53 mmol/L (95% CI; -2.17 to -0.88) [GRADE: moderate] and in systolic blood pressure levels by 3.64 mm Hg (95% CI -6.24 to -1.03). No significant effects on lipid profile and diastolic blood pressure were demonstrated. A significant increase in the risk for any hypoglycemia (RR: 2.62, 95% CI; 1.15-5.96, I = 33%) [GRADE: moderate] and for nausea (RR: 3.21, 95% CI; 1.36-7.54, I = 63%) [GRADE: moderate] and a non-significant increase in the risk for diarrhoea (RR: 1.64, 95% CI; 0.98-2.75, I = 0%) [GRADE: low] were documented. No other safety issues were identified.
This meta-analysis suggests that a GLP-1RA/SGLT-2i combination, if tolerated, exerts significant beneficial effects on glycemic control and body weight loss, however increasing the risk for any hypoglycemia and gastrointestinal adverse events.
钠-葡萄糖协同转运蛋白 2 抑制剂(SGLT-2i)和胰高血糖素样肽-1 受体激动剂(GLP-1RAs)目前被认为是 2 型糖尿病(T2DM)治疗的关键药物。本荟萃分析旨在提供关于 GLP-1RA 联合 SGLT-2i 治疗相较于单独使用 SGLT-2i 在安全性和疗效方面的更精确的效应估计。
从建库至 2019 年 5 月,通过检索 PubMed 和 CENTRAL 以及灰色文献来源,纳入持续时间≥12 周的随机对照试验(RCTs),评估在 T2DM 患者中,与单独使用 SGLT-2i 相比,SGLT-2i 联合最大剂量 GLP-1RA 的安全性和疗效。我们还使用推荐评估、制定与评价(GRADE)方法来评估我们汇总估计的可信度。
我们共纳入了 3 项符合条件的 RCT,总计纳入了 1042 例 T2DM 患者的数据。与单独使用 SGLT-2i 相比,SGLT-2i 联合最大剂量 GLP-1RA 治疗可使糖化血红蛋白降低 0.91%(95%CI:-1.41 至-0.42)[GRADE:中等]、体重降低 1.95kg(95%CI:-3.83 至-0.07)[GRADE:中等]、空腹血糖降低 1.53mmol/L(95%CI:-2.17 至-0.88)[GRADE:中等]和收缩压降低 3.64mmHg(95%CI:-6.24 至-1.03)。未观察到对血脂谱和舒张压的显著影响。低血糖(RR:2.62,95%CI:1.15-5.96,I²=33%)[GRADE:中等]和恶心(RR:3.21,95%CI:1.36-7.54,I²=63%)[GRADE:中等]的风险显著增加,而腹泻(RR:1.64,95%CI:0.98-2.75,I²=0%)[GRADE:低]的风险非显著增加。未发现其他安全性问题。
本荟萃分析提示,GLP-1RA/SGLT-2i 联合治疗,如果耐受,可显著改善血糖控制和体重减轻,但会增加低血糖和胃肠道不良事件的风险。