Systematic review and meta-analysis of vildagliptin for treatment of type 2 diabetes

被引:41
|
作者
Bekiari, Eleni [1 ,2 ]
Rizava, Chrysoula [1 ]
Athanasiadou, Eleni [1 ]
Papatheodorou, Konstantinos [2 ,3 ]
Liakos, Aris [1 ]
Karagiannis, Thomas [1 ]
Mainou, Maria [1 ]
Rika, Maria [2 ]
Boura, Panagiota [4 ]
Tsapas, Apostolos [1 ,2 ,5 ]
机构
[1] Aristotle Univ Thessaloniki, Clin Res & Evidence Based Med Unit, Dept Med 2, Hippokratio Gen Hosp, 49 Konstantinoupoleos St, Thessaloniki 54642, Greece
[2] Aristotle Univ Thessaloniki, Ctr Diabet, Dept Med 2, Thessaloniki 54642, Greece
[3] Democritus Univ Thrace, Dept Med 2, Alexandroupolis, Greece
[4] Aristotle Univ Thessaloniki, Dept Med 2, Thessaloniki 54642, Greece
[5] Univ Oxford, Harris Manchester Coll, Oxford, England
关键词
Vildagliptin; DPP-4; inhibitors; Systematic review; Meta-analysis; DRUG-NAIVE PATIENTS; IMPROVES GLYCEMIC CONTROL; SEVERE RENAL IMPAIRMENT; BETA-CELL FUNCTION; ADD-ON THERAPY; DPP-4 INHIBITOR VILDAGLIPTIN; DIPEPTIDYL PEPTIDASE-4 INHIBITORS; INDIVIDUALIZED TREATMENT TARGETS; METFORMIN COMBINATION THERAPY; RANDOMIZED CLINICAL-TRIALS;
D O I
10.1007/s12020-015-0841-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This systematic review and meta-analysis provides an update on the efficacy and safety of vildagliptin for treatment of type 2 diabetes mellitus (T2DM). We searched MEDLINE, COCHRANE, EMBASE and the drug manufacturer's website for randomised controlled trials of vildagliptin in patients with T2DM. Sixty-nine studies (28,006 patients) were included in the meta-analysis. Compared with placebo vildagliptin reduced HbA(1c) (weighted mean difference WMD -0.69 %; 95 % CI -0.83 to -0.56 %; I (2) = 82 %), and it was as effective as other antidiabetic agents (WMD -0.01 %; 95 % CI -0.16 to 0.14 %; I (2) = 93 %), without increasing the risk for hypoglycemia (OR 0.83; 95 % CI 0.59 to 1.16; I (2) = 0 % vs. placebo, and OR 0.19; 95 % CI 0.15 to 0.24; I (2) = 78 % versus active comparators). However, it was associated with an increase in the incidence of arthralgia compared with other comparators (OR 1.23; 95 % CI 1.02 to 1.48; I (2) = 0 %). On the contrary, vildagliptin did not increase the incidence of pancreatitis (OR 0.97; 95 % CI 0.37 to 2.53; I (2) = 0 %), serious adverse events (OR 0.98; 95 % CI 0.88 to 1.09; I (2) = 0 %) or death (OR 1.10, 95 % CI 0.75 to 1.61; I (2) = 0 %). Finally, odds ratio (OR) for heart failure, and overall cardiovascular and cerebrovascular events was 0.77 (95 % CI 0.46 to 1.30; I (2) = 0 %) and 0.91 (95 % CI 0.73 to 1.14; I (2) = 0 %), respectively. Vildagliptin is an effective and safe therapeutic option for patients with T2DM, both as monotherapy and as add-on treatment.
引用
收藏
页码:458 / 480
页数:23
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