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首页> 外文期刊>The Lancet >Rosiglitazone evaluated for cardiovascular outcomes in oral agent combination therapy for type 2 diabetes (RECORD): a multicentre, randomised, open-label trial.
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Rosiglitazone evaluated for cardiovascular outcomes in oral agent combination therapy for type 2 diabetes (RECORD): a multicentre, randomised, open-label trial.

机译:罗格列酮在2型糖尿病的口服药物联合治疗(RECORD)中评估了心血管结局:一项多中心,随机,开放标签试验。

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BACKGROUND: Rosiglitazone is an insulin sensitiser used in combination with metformin, a sulfonylurea, or both, for lowering blood glucose in people with type 2 diabetes. We assessed cardiovascular outcomes after addition of rosiglitazone to either metformin or sulfonylurea compared with the combination of the two over 5-7 years of follow-up. We also assessed comparative safety. METHODS: In a multicentre, open-label trial, 4447 patients with type 2 diabetes on metformin or sulfonylurea monotherapy with mean haemoglobin A(1c) (HbA(1c)) of 7.9% were randomly assigned to addition of rosiglitazone (n=2220) or to a combination of metformin and sulfonylurea (active control group, n=2227). The primary endpoint was cardiovascular hospitalisation or cardiovascular death, with a hazard ratio (HR) non-inferiority margin of 1.20. Analysis was by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00379769. FINDINGS: 321 people in the rosiglitazone group and 323 in the active control group experienced the primary outcome during a mean 5.5-year follow-up, meeting the criterion of non-inferiority (HR 0.99, 95% CI 0.85-1.16). HR was 0.84 (0.59-1.18) for cardiovascular death, 1.14 (0.80-1.63) for myocardial infarction, and 0.72 (0.49-1.06) for stroke. Heart failure causing admission to hospital or death occurred in 61 people in the rosiglitazone group and 29 in the active control group (HR 2.10, 1.35-3.27, risk difference per 1000 person-years 2.6, 1.1-4.1). Upper and distal lower limb fracture rates were increased mainly in women randomly assigned to rosiglitazone. Mean HbA(1c) was lower in the rosiglitazone group than in the control group at 5 years. INTERPRETATION: Addition of rosiglitazone to glucose-lowering therapy in people with type 2 diabetes is confirmed to increase the risk of heart failure and of some fractures, mainly in women. Although the data are inconclusive about any possible effect on myocardial infarction, rosiglitazone does not increase the risk of overall cardiovascular morbidity or mortality compared with standard glucose-lowering drugs. FUNDING: GlaxoSmithKline plc, UK.
机译:背景:罗格列酮是一种胰岛素增敏剂,与二甲双胍,磺酰脲或两者合用,可降低2型糖尿病患者的血糖。我们将罗格列酮加到二甲双胍或磺脲类药物中后,与两者在5-7年的随访组合相结合,评估了心血管结局。我们还评估了比较安全性。方法:在一项多中心,开放性试验中,将4447例接受二甲双胍或磺酰脲单药治疗,平均血红蛋白A(1c)(HbA(1c))为7.9%的2型糖尿病患者随机分配为罗格列酮治疗(n = 2220)或二甲双胍和磺脲类药物的组合(有效对照组,n = 2227)。主要终点为心血管住院或心血管死亡,危险比(HR)的非劣效性为1.20。分析是按意向进行的。该研究已在ClinicalTrials.gov上注册,编号为NCT00379769。结果:罗格列酮组中的321人和活动对照组中的323人在平均5.5年的随访期间经历了主要结局,符合非自卑的标准(HR 0.99,95%CI 0.85-1.16)。心血管死亡的HR为0.84(0.59-1.18),心肌梗塞的HR为1.14(0.80-1.63),中风的为0.72(0.49-1.06)。罗格列酮组有61人发生心衰,导致死亡或死亡,而活动对照组则有29人(HR 2.10、1.35-3.27,每千人年风险差异2.6、1.1-4.1)。随机分配罗格列酮的女性上,下肢远端骨折率增加。罗格列酮组5年平均HbA(1c)低于对照组。解释:在2型糖尿病患者中,在降低葡萄糖的治疗中加入罗格列酮已被证实会增加心力衰竭和某些骨折的风险,主要是女性。尽管数据尚不确定对心肌梗塞的任何可能影响,但与标准降糖药物相比,罗格列酮不会增加整体心血管疾病或死亡的风险。资金:英国葛兰素史克公司。

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