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Saxagliptin combined with additional oral antihyperglycaemic agents in drug-naive diabetic patients with high glycosylated haemoglobin: A 24-week, multicentre, randomized, open-label, active parallel-controlled group clinical trial in China (SUCCESS)

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单位: [1]China Japan Friendship Hosp, Dept Endocrinol, 2 Yinghua East St, Beijing 100029, Peoples R China [2]Henan Univ Sci & Technol, Affiliated Hosp 1, Dept Endocrinol, Luoyang, Peoples R China [3]Emergency Gen Hosp, Dept Endocrinol, Beijing, Peoples R China [4]Harbin Med Univ, Affiliated Hosp 1, Dept Endocrinol, Harbin, Peoples R China [5]Shandong Univ, Qilu Hosp, Dept Endocrinol, Jinan, Peoples R China [6]Nanjing First Hosp, Dept Endocrinol, Nanjing, Peoples R China [7]Anhui Med Univ, Affiliated Hosp 1, Dept Endocrinol, Hefei, Peoples R China [8]Anhui Med Univ, Affiliated Hosp 2, Dept Endocrinol, Hefei, Peoples R China
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关键词: combination therapy glycaemic control newly diagnosed oral antidiabetics type 2 diabetes

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Aim To assess the efficacy and safety of a dipeptidyl peptidase-4 (DPP-4) inhibitor combined respectively with three oral antihyperglycaemic agents in Chinese patients with newly diagnosed type 2 diabetes mellitus (T2DM) with high levels of glycated haemoglobin (HbA1c). Materials and methods Between 30 December 2014 and 1 November 2017, a 24-week, multicentre, parallel-controlled study was performed on drug-naive T2DM patients. In total, 648 patients with 8.0% <= HbA1c <= 11.0%, aged 18-80 years and body mass index (BMI) 19-40 kg/m(2) were randomly assigned 1:1:1 to receive saxagliptin (Saxa) combined with metformin (Met), acarbose (Aca) or gliclazide (Gli) modified release (MR) tablets (Saxa + Met, Saxa + Aca and Saxa + Gli). The primary outcome was the absolute change in HbA1c from baseline; secondary outcome was the percentage of patients achieving HbA1c Each treatment arm contained 216 patients; overall, 583 completed the 24-week trial. At 24 weeks, the mean (95% confidence interval) change in HbA1c from baseline in Saxa + Met, Saxa + Aca and Saxa + Gli were, respectively: -2.9% [-3.1, -2.8]; -2.6% [-2.8, -2.5]; and -2.8% [-2.9, -2.6] (overall p = .04, Saxa + Aca vs. Saxa + Met, p = .010, Saxa + Gli vs. Saxa + Met, p = 0.18). At 24 weeks, 84.9%, 74.7% and 80.3% of participants were at HbA1c <7.0% (overall p = .05); and 72.6%, 59.8% and 63.3% were HbA1c <= 6.5% (overall p = 0.10). The rates of minor or symptomatic hypoglycaemia were very low. Conclusions Initial treatment with a DPP-4 inhibitor combined with Metform, alpha-glycosidase inhibitor or sulphonylurea was safe and effective for patients with newly diagnosed T2DM and high HbA1c. DPP-4 inhibitor combined with Met showed the best efficacy for this population.

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出版当年[2021]版:
大类 | 2 区 医学
小类 | 2 区 内分泌学与代谢
最新[2025]版:
大类 | 2 区 医学
小类 | 2 区 内分泌学与代谢
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出版当年[2020]版:
Q1 ENDOCRINOLOGY & METABOLISM
最新[2023]版:
Q1 ENDOCRINOLOGY & METABOLISM

影响因子: 最新[2023版] 最新五年平均[2021-2025] 出版当年[2020版] 出版当年五年平均[2016-2020] 出版前一年[2019版] 出版后一年[2021版]

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第一作者单位: [1]China Japan Friendship Hosp, Dept Endocrinol, 2 Yinghua East St, Beijing 100029, Peoples R China
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通讯机构: [1]China Japan Friendship Hosp, Dept Endocrinol, 2 Yinghua East St, Beijing 100029, Peoples R China [*1]Department of Endocrinology,China-Japan Friendship Hospital,No. 2 Yinghua East Street, Chaoyang District,Beijing, 100029, People's Republic of China.
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