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首页> 外文期刊>Diabetes, obesity & metabolism >Effect of ertugliflozin on glucose control, body weight, blood pressure and bone density in type 2 diabetes mellitus inadequately controlled on metformin monotherapy ( VERTIS MET VERTIS MET )
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Effect of ertugliflozin on glucose control, body weight, blood pressure and bone density in type 2 diabetes mellitus inadequately controlled on metformin monotherapy ( VERTIS MET VERTIS MET )

机译:2型糖尿病型葡萄牙对照,体重,血压和骨密度对二甲双胍单疗法(Vertis Met Verti)对糖尿病患者葡萄糖对照,体重,血压和骨密度的影响

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Aim We evaluated the efficacy and safety of ertugliflozin, an SGLT2 inhibitor, in type 2 diabetes mellitus (T2DM) inadequately controlled (HbA1c, 7.0%‐10.5%) with metformin monotherapy (≥1500?mg/d for ≥8?weeks). Methods This was a double‐blind, 26‐week, multicentre study with ongoing 78‐week extension ( ClinicalTrials.gov identifier: NCT02033889). A total of 621 participants were randomized 1:1:1 to placebo, or ertugliflozin 5 or 15?mg/d. The primary endpoint was change from baseline at week 26 in HbA1c. Secondary efficacy endpoints were change from baseline at week 26 in fasting plasma glucose (FPG), body weight, systolic/diastolic blood pressure (SBP/DBP) and number of participants with HbA1c 7.0% (53?mmol/mol). Pre‐specified adverse events (AEs) of special interest and percent change from baseline in bone mineral density (BMD) were also assessed at week 26. Results At week 26, the placebo‐adjusted least‐squares mean change from baseline HbA1c (8.1%) was ?0.7% and ?0.9% for ertugliflozin 5 and 15?mg, respectively (both P ??.001), to final means of 7.3% and 7.2%, respectively. The odds of HbA1c 7.0% were significantly greater in both ertugliflozin groups vs placebo. Ertugliflozin significantly reduced FPG, body weight, SBP and DBP vs placebo. The incidence of genital mycotic infections was higher in the ertugliflozin groups (female subjects: placebo, 0.9%; ertugliflozin 5?mg, 5.5%; ertugliflozin 15?mg, 6.3% [ P ?=?.032]; male subjects: 0%; 3.1%; 3.2%, respectively), as was the incidence of urinary tract infections and symptomatic hypoglycaemia. The incidence of hypovolaemia AEs was similar across groups. Ertugliflozin had no adverse impact on BMD at week 26. Conclusions Ertugliflozin added to metformin in patients with inadequately controlled T2DM improved glycaemic control, reduced body weight and BP, but increased the incidence of genital mycotic infections.
机译:目的:我们评估SGLT2抑制剂厄特格列嗪在二甲双胍单药治疗未得到充分控制的2型糖尿病(T2DM)中的疗效和安全性(HbA1c,7.0%-10.5%)(≥1500?毫克/日≥8.周)。方法这是一项双盲、26周、多中心研究,持续78周(ClinicalTrials.gov标识符:NCT02033889)。共有621名受试者按1:1:1的比例随机分为安慰剂组、厄特格列嗪5组或15组?mg/d。主要终点是HbA1c在第26周与基线检查时的变化。次要疗效终点是在第26周空腹血糖(FPG)、体重、收缩压/舒张压(SBP/DBP)和糖化血红蛋白(HbA1c)患者人数与基线相比的变化;7.0%(53 mmol/mol)。在第26周,还评估了特别关注的预先指定的不良事件(AE)和骨密度(BMD)相对于基线的百分比变化。结果在第26周,安慰剂调整后的最小平方平均值与基线HbA1c(8.1%)相比变化为?0.7%和?ertugliflozin 5和15为0.9%?mg,分别为7.3%和7.2%。糖化血红蛋白的几率;厄特格列嗪组和安慰剂组的7.0%显著高于安慰剂组。与安慰剂相比,厄图格列嗪显著降低空腹血糖、体重、收缩压和舒张压。厄图格列嗪组的生殖道真菌感染发生率较高(女性受试者:安慰剂,0.9%;厄图格列嗪5?mg,5.5%;厄图格列嗪15?mg,6.3%[P?=?.032];男性受试者:0%;3.1%;3.2%),尿路感染和症状性低血糖的发生率也较高。各组间低血容量不良事件的发生率相似。在第26周,厄图格列嗪对BMD没有不良影响。结论二甲双胍联合厄特格列嗪治疗控制不充分的T2DM患者,可改善血糖控制,降低体重和血压,但增加生殖道真菌感染的发生率。

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