Buysschaert Martin, D'Hooge Dirk, Preumont Vanessa
Department of Endocrinology and Diabetology, Université catholique de Louvain, University Clinic St-Luc, Brussels, Belgium.
Novo Nordisk Pharma Belux, Brussels, Belgium.
Diabetes Metab Syndr. 2015 Jul-Sep;9(3):139-42. doi: 10.1016/j.dsx.2015.05.001. Epub 2015 May 8.
The ROOTS study was an observational study to evaluate the effectiveness and safety of liraglutide (Victoza(®)), a GLP-1 receptor analog, in a cohort of patients with type 2 diabetes with inadequate glycaemic control despite conventional antihyperglycaemic dual therapy. The primary objective was to assess glycaemic control while using liraglutide under normal clinical practice conditions. The primary endpoint was to estimate the proportion of patients achieving improved glycaemic control defined as a HbA1c<7% or with a decrease of ≥1% after 12 months.
The study included 245 subjects. They received liraglutide in addition to their usual dual therapy (metformin and sulfonylureas or pioglitazone). Age and duration (mean±SD) of diabetes were 58±10 and 9±5 years respectively. Body mass index was 33.9±6.2 kg/m(2).
HbA1c decreased from 9.12%±1.28 at baseline to 7.54%±1.12 after one year follow-up (p<0.001). The primary endpoint was achieved in 66.5% of patients. In parallel, we observed a reduction of BMI from baseline 33.9±6.2 to 32.8±6.3 kg/m(2) (p<0.001). At 12 months, 64.6% of the patients received liraglutide at a dosage of 1.2 mg/day, 32.7% received 1.8 mg and 2.7% 0.6 mg. Adverse drug reactions were present in 24% of subjects, most frequently gastrointestinal disorders (11.4%), mainly nausea (6.9%) and no pancreatic events.
Treatment with liraglutide was associated with a marked improvement in glycaemic control in daily routine practice as well as with a reduction of weight, without major side effects.
ROOTS研究是一项观察性研究,旨在评估胰高血糖素样肽-1(GLP-1)受体类似物利拉鲁肽(Victoza(®))在一组尽管接受了传统双联降糖治疗但血糖控制不佳的2型糖尿病患者中的有效性和安全性。主要目的是在正常临床实践条件下使用利拉鲁肽时评估血糖控制情况。主要终点是估计在12个月后糖化血红蛋白(HbA1c)<7%或下降≥1%从而实现血糖控制改善的患者比例。
该研究纳入了245名受试者。他们在接受常规双联治疗(二甲双胍和磺脲类药物或吡格列酮)的基础上还接受了利拉鲁肽治疗。糖尿病患者的年龄和病程(平均值±标准差)分别为58±10岁和9±5年。体重指数为33.9±6.2kg/m²。
随访一年后,糖化血红蛋白(HbA1c)从基线时的9.12%±1.28%降至7.54%±1.12%(p<0.001)。66.5%的患者达到了主要终点。同时,我们观察到体重指数从基线时的33.9±6.2降至32.8±6.3kg/m²(p<0.001)。在12个月时,64.6%的患者接受1.2mg/天剂量的利拉鲁肽治疗,32.7%接受1.8mg治疗,2.7%接受0.6mg治疗。24%的受试者出现药物不良反应,最常见的是胃肠道疾病(11.4%),主要是恶心(6.9%),未出现胰腺相关事件。
在日常临床实践中,利拉鲁肽治疗与血糖控制的显著改善以及体重减轻相关,且无严重副作用。