Liu Xin, Men Peng, Wang Yuhui, Zhai Suodi, Liu George
Institute of Cardiovascular Sciences, School of Basic Medical Science, Peking University Health Science Center, 38 Xueyuan Road, Beijing, 100191, China.
Department of Pharmacy, Peking University Third Hospital, Beijing, China.
Lipids Health Dis. 2016 Nov 23;15(1):204. doi: 10.1186/s12944-016-0372-7.
Adiponectin, an adipose-specific protein, is negatively correlated with pro-atherogenic low-density lipoprotein cholesterol (LDL-C) and other cardiovascular risk factors such as insulin resistance. Therefore, low levels of adiponectin are associated with a higher risk for diabetes and cardiovascular disease. Dipeptidyl peptidase-4 inhibitors (DPP4i) have been used for the treatment of type 2 diabetes mellitus (T2DM) as reversible inhibitors through interacting with DPP4 substrate and increase serum incretins such as glucagon-like peptide-1 (GLP-1). The present study aimed to evaluate the effect of DPP4i on serum adiponectin in T2DM patients.
The PubMed, Embase, and Cochrane library databases were searched from inception to February 2016. Randomized controlled trials, evaluating the DPP4i (sitagliptin and vildagliptin) versus comparator (placebo or active-comparison), in T2DM patients with duration of ≥ 12 weeks, were identified. Weighted differences in means of adiponectin levels were calculated by using a fixed or random-effects model.
Ten randomized controlled trials, including 1,495 subjects, were identified. Compared with placebo, DPP4i (sitagliptin and vildagliptin) treatment significantly elevated adiponectin levels by 0.74 μg/mL (95% confidence interval [CI], 0.45 to 1.03) relative to that using an active-comparison by 0.00 μg/mL (95% CI, -0.57 to 0.56). Compared with active-comparison, vildagliptin treatment increased adiponectin levels by 0.32 μg/mL (95% CI, -0.01 to 0.65), whereas sitagliptin treatment decreased adiponectin levels by -0.24 μg/mL (95% CI, -1.07 to 0.58). Trials examining effects of other DPP4i were not found.
Sitagliptin and vildagliptin increased serum adiponectin levels and had no stronger effect than traditional oral antidiabetic drugs. Further trials with larger sample size are needed to confirm the results and investigate the association between serum adiponectin levels and treatment of other DPP-4 inhibitors.
Registration No in PROSPERO: CRD42016037399 .
脂联素是一种脂肪特异性蛋白,与促动脉粥样硬化的低密度脂蛋白胆固醇(LDL-C)及其他心血管危险因素(如胰岛素抵抗)呈负相关。因此,脂联素水平较低与糖尿病和心血管疾病的较高风险相关。二肽基肽酶-4抑制剂(DPP4i)已被用作2型糖尿病(T2DM)的治疗药物,通过与DPP4底物相互作用作为可逆抑制剂,并增加血清肠促胰岛素,如胰高血糖素样肽-1(GLP-1)。本研究旨在评估DPP4i对T2DM患者血清脂联素的影响。
检索PubMed、Embase和Cochrane图书馆数据库,检索时间从建库至2016年2月。纳入评估DPP4i(西他列汀和维格列汀)与对照(安慰剂或活性对照)相比,用于病程≥12周的T2DM患者的随机对照试验。采用固定效应模型或随机效应模型计算脂联素水平均值的加权差异。
共纳入10项随机对照试验,包括1495名受试者。与安慰剂相比,DPP4i(西他列汀和维格列汀)治疗使脂联素水平相对于活性对照显著升高0.74μg/mL(95%置信区间[CI],0.45至1.03),而活性对照升高0.00μg/mL(95%CI,-0.57至0.56)。与活性对照相比,维格列汀治疗使脂联素水平升高0.32μg/mL(95%CI,-0.01至0.65),而西他列汀治疗使脂联素水平降低-0.24μg/mL(95%CI,-1.07至0.58)。未发现考察其他DPP4i效果的试验。
西他列汀和维格列汀可提高血清脂联素水平,且效果不比传统口服降糖药更强。需要进一步开展更大样本量的试验来证实结果,并研究血清脂联素水平与其他DPP-4抑制剂治疗之间的关联。
PROSPERO注册号:CRD42016037399 。