Saxagliptin and sitagliptin in adult patients with type 2 diabetes: a systematic review and meta-analysis

被引:22
作者
Gerrald, K. R. [1 ]
Van Scoyoc, E. [2 ]
Wines, R. C. [3 ]
Runge, T. [4 ]
Jonas, D. E. [5 ]
机构
[1] Presbyterian Coll, Sch Pharm, Dept Pharm Practice, Clinton, SC USA
[2] Brown Alpert Med Sch, Dept Pediat, Providence, RI USA
[3] Univ N Carolina, Cecil G Sheps Ctr Hlth Serv Res, RTI UNC Evidence Based Practice Ctr, Chapel Hill, NC USA
[4] Univ N Carolina, Sch Med, Chapel Hill, NC USA
[5] Univ N Carolina, Dept Med, Chapel Hill, NC USA
关键词
DPP-4; inhibitor; meta-analysis; type; 2; diabetes; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; INITIAL COMBINATION THERAPY; ONGOING METFORMIN THERAPY; GLYCEMIC CONTROL; JAPANESE PATIENTS; DOUBLE-BLIND; EFFICACY; SAFETY; MONOTHERAPY; SULFONYLUREA;
D O I
10.1111/j.1463-1326.2011.01540.x
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The objective of this study is to compare the efficacy and safety of sitagliptin and saxagliptin with placebo and other hypoglycaemic medications in adults with type 2 diabetes. We searched MEDLINE (R), Embase, the Cochrane Library and the International Pharmaceuticals from their inception through 3 February 2011. Studies were included of adults with type 2 diabetes that were 12 weeks or more in duration. Meta-analyses were conducted when included studies were homogenous enough to justify combining their results. A total of 32 articles met inclusion criteria. Sitagliptin 100 mg monotherapy and saxagliptin 5 mg resulted in greater HbA1c reduction compared to placebo [weighted mean difference (WMD) -0.82%, 95% CI -0.95 to -0.70 and WMD -0.70, 95% CI -0.84 to -0.56, respectively]. Sitagliptin was similar to sulfonylureas for HbA1c reduction (WMD 0.08%, 95% CI 00.16, 3 trials) and to saxagliptin in one head-to-head trial. There was no statistically significant difference in hypoglycaemia between sitagliptin (pooled RR 1.55, 95% CI 0.554.36) or saxagliptin (pooled RR 1.04, 95% CI 0.283.81) and placebo. Sitagliptin and saxagliptin result in similar modest HbA1c reductions and do not increase the risk of hypoglycaemia unless combined with other therapies. Their role in the long-term treatment of type 2 diabetes remains unclear given the lack of long-term data on efficacy, harms and health outcomes.
引用
收藏
页码:481 / 492
页数:12
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