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Clinical Effectiveness of Liraglutide vs Sitagliptin on Glycemic Control and Body Weight in Patients with Type 2 Diabetes: A Retrospective Assessment in Sweden

机译:利拉鲁肽和西他列汀对2型糖尿病患者血糖控制和体重的临床效果:瑞典的回顾性评估

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Introduction: The aim of the present study was to use real-world data from Swedish primary-care and national registries to understand clinical outcomes in patients with Type 2 diabetes (T2D) treated with liraglutide in clinical practice, and to compare with data from those treated with sitagliptin. Methods: This was a non-interventional, retrospective study conducted between February 2014 and September 2014 using T2D patient data from Swedish primary-care centers and national healthcare registries. The primary objective was to assess the effectiveness of liraglutide in control of glycemia and body weight in clinical practice (stage 1). The secondary objective was to compare the clinical effectiveness of liraglutide with sitagliptin on glycemic control and body weight in clinical practice in a propensity-score-matched population (stage 2). Results: In stage 1 (n = 402), 39.4% of patients treated with liraglutide achieved ≥1.0% (10.9 mmol/mol) reduction in glycated hemoglobin (HbA1c) after 180 days of treatment and 54.9% achieved the target HbA1c of <7.0% (53.0 mmol/mol). Moreover, compared with baseline, 22.5% of patients treated with liraglutide achieved both ≥1.0% reduction in HbA1c and ≥3.0% reduction in body weight. In stage 2, a significantly greater proportion of patients receiving liraglutide (n = 180) than sitagliptin (n = 208) achieved ≥1.0% reduction in HbA1c [52.9% vs 33.5%, respectively (P = 0.0002)]. Mean body-weight loss was also significantly greater in patients receiving liraglutide vs sitagliptin [?3.5 vs ?1.3 kg, respectively (P < 0.0001)]. Conclusion: This study provides real-world evidence from Sweden corroborating previous clinical trials that demonstrate greater efficacy of liraglutide over sitagliptin on glycemic control and body-weight reduction in patients with T2D. Funding: Novo Nordisk A/S. Trial registration: ClinicalTrials.gov identifier NCT02077946.
机译:简介:本研究的目的是利用瑞典初级保健机构和国家注册机构的真实数据来了解利拉鲁肽治疗的2型糖尿病(T2D)患者的临床结局,并与这些数据进行比较西他列汀治疗。方法:这是一项2014年2月至2014年9月之间进行的非干预性回顾性研究,使用了来自瑞典基层医疗中心和国家医疗机构的T2D患者数据。主要目的是评估临床实践中利拉鲁肽在控制血糖和体重方面的有效性(第1阶段)。次要目标是在倾向评分匹配的人群中比较利拉鲁肽和西他列汀在临床实践中对血糖控制和体重的临床效果(阶段2)。结果:在第1阶段(n = 402),治疗180天后39.4%的利拉鲁肽治疗的患者糖化血红蛋白(HbA1c)降低≥1.0%(10.9 mmol / mol),54.9%的患者目标HbA1c低于7.0 %(53.0 mmol / mol)。此外,与基线相比,接受利拉鲁肽治疗的患者中有22.5%的HbA1c降低了≥1.0%,体重降低了≥3.0%。在第2阶段,接受利拉鲁肽(n = 180)的患者比例比西他列汀(n = 208)明显多于HbA1c降低≥1.0%[分别为52.9%和33.5%(P = 0.0002)]。利拉鲁肽组与西他列汀组相比,平均体重减轻也显着更大(分别为?3.5 vs?1.3 kg(P <0.0001))。结论:这项研究提供了来自瑞典的真实证据,佐证了先前的临床试验,这些结果表明利拉鲁肽优于西他列汀在T2D患者的血糖控制和体重减轻方面具有更大的疗效。资金来源:Novo Nordisk A / S。试用注册:ClinicalTrials.gov标识符NCT02077946。

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