Bossi Antonio C, De Mori Valentina, Scaranna Cristiana, Veronesi Giovanni, Lepore Giuseppe
ASST Bergamo Ovest, Treviglio, BG, Italy.
ASST Papa Giovanni XXIII, Bergamo, Italy.
Diabetes Ther. 2020 Nov;11(11):2677-2690. doi: 10.1007/s13300-020-00929-4. Epub 2020 Sep 24.
Dulaglutide, a long-acting glucagon-like peptide-1 receptor agonist (GLP-1RA), became available in Italy in April 2016. The aim of ANDREW (Active Notes on Dulaglutide in the REal World), a multicenter, prospective, observational study, was to evaluate glycemic control and weight (co-primary outcomes) for up to 24 months in the real-life setting in consecutive outpatients with type 2 diabetes (T2D) who initiated dulaglutide. Co-secondary outcomes were durability of treatment effects on both glycated hemoglobin (HbA1c) and body weight.
Overall, 1584 subjects (696 women, 888 men) with T2D (mean age [± standard deviation] 61.7 ± 10.2 years; mean T2D duration 9.9 ± 6.9 years) were treated with dulaglutide (0.75 or 1.5 mg once weekly) between April 2016 and December 2019.
A total of 1130 patients completed 12 months of follow-up, while 170 patients interrupted treatment before the 12-month endpoint. At 12 months, average HbA1c and average fasting plasma glucose (FPG) were significantly lower compared to baseline levels (- 10 mmol/mol and - 24.9 mg/dL, respectively), as were body weight (- 3.4 kg) and waist circumference (- 3.3 cm) values (all p < 0.0001). Among subjects that completed 24 months of follow-up (n = 270), the rapid decline in HbA1c and FPG values in the first 12 months was followed by stabilization in the following 12 months (p value for 12-24 months trend: 0.4 and 0.6, respectively).
Dulaglutide is an effective drug for the treatment of T2D that is administered once weekly using a simple auto-injector device. Real-life data confirm the observations in randomized controlled trials that persistent treatment with dulaglutide may help patients with T2D achieve an improvement in some metabolic features and in body weight. It is important that the benefits of therapy with dulaglutide, i.e., the effects of the "glycemic" and the so-called "extra-glycemic" actions of GLP-1RAs, are supported by diabetes care teams emphasizing the need for patients to maintain a healthy lifestyle.
度拉糖肽是一种长效胰高血糖素样肽-1受体激动剂(GLP-1RA),于2016年4月在意大利上市。ANDREW(度拉糖肽在现实世界中的活性记录)是一项多中心、前瞻性、观察性研究,其目的是评估在现实生活环境中,连续使用度拉糖肽的2型糖尿病(T2D)门诊患者长达24个月的血糖控制情况和体重(共同主要结局)。次要共同结局是治疗对糖化血红蛋白(HbA1c)和体重的疗效持久性。
2016年4月至2019年12月期间,共有1584例T2D患者(696例女性,888例男性)接受度拉糖肽治疗(0.75或1.5mg,每周一次)(平均年龄[±标准差]61.7±10.2岁;平均T2D病程9.9±6.9年)。
共有1130例患者完成了12个月的随访,170例患者在12个月终点前中断治疗。在12个月时,平均HbA1c和平均空腹血糖(FPG)与基线水平相比显著降低(分别降低-10mmol/mol和-24.9mg/dL),体重(-3.4kg)和腰围(-3.3cm)值也是如此(所有p<0.0001)。在完成24个月随访的受试者(n=270)中,HbA1c和FPG值在最初12个月快速下降,随后12个月趋于稳定(12-24个月趋势的p值分别为0.4和0.6)。
度拉糖肽是一种治疗T2D的有效药物,可使用简单的自动注射装置每周给药一次。现实生活数据证实了随机对照试验中的观察结果,即持续使用度拉糖肽可能有助于T2D患者改善某些代谢特征和体重。糖尿病护理团队强调患者需要保持健康的生活方式,这对度拉糖肽治疗的益处(即GLP-1RAs的“血糖”和所谓“血糖外”作用的效果)提供支持非常重要。