Sun Yu-Nan, Zhou Yi, Chen Xi, Che Weng-Si, Leung Siu-Wai
State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao, China.
BMJ Open. 2014 Apr 7;4(4):e004619. doi: 10.1136/bmjopen-2013-004619.
This meta-analysis aimed to evaluate whether dapagliflozin is synergistic with other antidiabetic drugs without body weight gain.
Randomised controlled trial (RCT) reports were retrieved from PubMed, Cochrane Library, EMBASE, ClinicalTrials.gov, Google Scholar and Google. Eligible RCTs were selected according to the criteria (including types of participants, intervention, outcomes) and assessed by the Cochrane risk of bias tool and GRADEpro software for evidential quality. Meta-analysis on the eligible RCTs was performed with the random effects model. The RCTs of low-quality and interim stages were excluded for further sensitivity analysis. Meta-regression was conducted on the follow-up durations. Publication bias was evaluated with funnel plots and the Egger's regression test and adjusted using the trim-and-fill procedure. Heterogeneity was assessed with the I(2) statistics.
Adult patients with type 2 diabetes mellitus (T2DM).
Dapagliflozin combined with conventional antidiabetic drugs.
Glycaemic level (measured by glycosylated haemoglobin (HbA1c) and fasting plasma glucose (FPG)) and body weight.
12 RCTs were eligible for quantitative synthesis and meta-analysis. The overall effect size of HbA1c calculated from mean difference was -0.52% (Z=-13.56, p<0.001) with 95% CI (-0.60 to -0.45). The effect size of FPG was -1.13 mmol/L (Z=-11.12, p<0.001) with 95% CI (-1.33 to -0.93). The effect size of body weight was -2.10 kg (Z=-18.77, p<0.001) with 95% CI (-2.32 to -1.88). Exclusions of low quality and interim RCTs changed the overall mean differences respectively to -0.56%, -1.11 mmol/L, 2.23 kg and -0.50%, -1.08 mmol/L, -2.08 kg. The sensitivity analysis indicated good robustness of the meta-analysis on HbA1c, FPG and body weight.
The meta-analysis showed that dapagliflozin as an add-on drug to conventional antidiabetic drugs improved the glycaemic control in T2DM participants without significant body weight gain.
CRD42013005034.
本荟萃分析旨在评估达格列净与其他抗糖尿病药物联合使用时是否具有协同作用且不会导致体重增加。
从PubMed、Cochrane图书馆、EMBASE、ClinicalTrials.gov、谷歌学术和谷歌中检索随机对照试验(RCT)报告。根据标准(包括参与者类型、干预措施、结局指标)选择符合条件的RCT,并通过Cochrane偏倚风险工具和GRADEpro软件评估证据质量。对符合条件的RCT进行随机效应模型的荟萃分析。排除低质量和中期阶段的RCT进行进一步的敏感性分析。对随访时间进行荟萃回归分析。使用漏斗图和Egger回归检验评估发表偏倚,并采用修剪填充法进行调整。用I²统计量评估异质性。
成年2型糖尿病(T2DM)患者。
达格列净与传统抗糖尿病药物联合使用。
血糖水平(通过糖化血红蛋白(HbA1c)和空腹血糖(FPG)测量)和体重。
12项RCT符合定量合成和荟萃分析的条件。根据平均差异计算的HbA1c总体效应量为-0.52%(Z = -13.56,p < 0.001),95%置信区间为(-0.60至-0.45)。FPG的效应量为-1.13 mmol/L(Z = -11.12,p < 0.001),95%置信区间为(-1.33至-0.93)。体重的效应量为-2.10 kg(Z = -18.77,p < 0.001),95%置信区间为(-2.32至-1.88)。排除低质量和中期RCT后,总体平均差异分别变为-0.56%、-1.11 mmol/L、2.23 kg和-0.50%、-1.08 mmol/L、-2.08 kg。敏感性分析表明荟萃分析对HbA1c、FPG和体重具有良好的稳健性。
荟萃分析表明,达格列净作为传统抗糖尿病药物的附加药物可改善T2DM参与者的血糖控制,且不会显著增加体重。
CRD42013005034。