Chan Siew Pheng, Colagiuri Stephen
Department of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
The Boden Institute, University of Sydney, Sydney, NSW, Australia.
Diabetes Res Clin Pract. 2015 Oct;110(1):75-81. doi: 10.1016/j.diabres.2015.07.002. Epub 2015 Jul 9.
Sulfonylureas are well positioned in treating type 2 diabetes, after lifestyle modification and metformin. The sulfonylurea gliclazide was given preference over glibenclamide in older people with type 2 diabetes in the World Health Organization model list of essential medicines. Consequently, a systematic review and meta-analysis of randomized controlled trials of the efficacy and safety of gliclazide versus other oral insulinotropic agents (sulfonylureas, dipeptidyl peptidase-4 inhibitors, and glinides) was performed.
Two reviewers searched MEDLINE for studies of ≥12 weeks duration in adults with type 2 diabetes. The key search word was "gliclazide", filtered with "randomized controlled trial", "human" and "19+ years". Differences were explored in mean change in glycated hemoglobin (HbA(1c)) from baseline (primary outcome) and risk of hypoglycemia (secondary outcome) between gliclazide and other oral insulinotropic agents; and other sulfonylureas.
Nine out of 181 references reported primary outcomes, of which 7 reported secondary outcomes. Gliclazide lowered HbA1c more than other oral insulinotropic agents, with a weighted mean difference of -0.11% (95%, CI -0.19 to -0.03%, P=0.008, I(2)=60%), though not more than other sulfonylureas (-0.12%; 95%, CI -0.25 to 0.01%, P=0.07, I(2)=77%). Risk of hypoglycemia with gliclazide was not different to other insulinotropic agents (RR 0.85; 95%, CI 0.66 to 1.09, P=0.20, I(2)=61%) but significantly lower than other sulfonylureas (RR 0.47; 95%, CI 0.27 to 0.79, P=0.004, I(2)=0%).
Compared with other oral insulinotropic agents, gliclazide significantly reduced HbA1c with no difference regarding hypoglycemia risk. Compared with other sulfonylureas, HbA1c reduction with gliclazide was not significantly different, but hypoglycemia risk was significantly lower.
在生活方式干预和二甲双胍治疗之后,磺脲类药物在2型糖尿病治疗中占据重要地位。在世界卫生组织基本药物示范清单中,对于老年2型糖尿病患者,格列齐特比格列本脲更受青睐。因此,针对格列齐特与其他口服促胰岛素分泌剂(磺脲类、二肽基肽酶-4抑制剂和格列奈类)疗效和安全性的随机对照试验进行了一项系统评价和荟萃分析。
两名评价者在MEDLINE中检索针对2型糖尿病成年患者、持续时间≥12周的研究。关键检索词为“格列齐特”,并通过“随机对照试验”“人类”和“19岁及以上”进行筛选。探讨了格列齐特与其他口服促胰岛素分泌剂以及其他磺脲类药物之间糖化血红蛋白(HbA1c)自基线的平均变化差异(主要结局)和低血糖风险差异(次要结局)。
181篇参考文献中有9篇报告了主要结局,其中7篇报告了次要结局。与其他口服促胰岛素分泌剂相比,格列齐特降低HbA1c的效果更显著,加权平均差为-0.11%(95%置信区间为-0.19至-0.03%,P = 0.008,I² = 60%),不过不比其他磺脲类药物更显著(-0.12%;95%置信区间为-0.25至0.01%,P = 0.07,I² = 77%)。格列齐特导致低血糖的风险与其他促胰岛素分泌剂无差异(相对危险度0.85;95%置信区间为0.66至1.09,P = 0.20,I² = 61%),但显著低于其他磺脲类药物(相对危险度0.47;95%置信区间为0.27至0.79,P = 0.004,I² = 0%)。
与其他口服促胰岛素分泌剂相比,格列齐特显著降低HbA1c,且低血糖风险无差异。与其他磺脲类药物相比,格列齐特降低HbA1c的效果无显著差异,但低血糖风险显著更低。