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Dipeptidyl peptidase 4 (DPP-4) inhibitors and cardiovascular outcomes in patients with type 2 diabetes mellitus (T2DM): a systematic review and meta-analysis.
BMC Pharmacology and Toxicology ( IF 2.605 ) Pub Date : 2019-03-06 , DOI: 10.1186/s40360-019-0293-y
Dan Liu 1 , Biao Jin 2 , Wei Chen 2 , Peng Yun 1
Affiliation  

BACKGROUND Dipeptidyl peptidase 4 (DPP-4) inhibitors are newer oral anti-diabetic agents which have been approved by the Food and Drug Administration for the treatment of patients with type 2 diabetes mellitus (T2DM). In this analysis, we aimed to systematically compare the cardiovascular outcomes associated with DPP-4 inhibitors versus non-DPP-4 inhibitor users. METHODS All English publications that compared the use of DPP-4 inhibitors and that reported cardiovascular outcomes in patients with T2DM were searched using specific terms. Studies were included if they satisfied the following inclusion criteria: They were randomized trials or observation cohorts/registries comparing DPP-4 inhibitors use in patients with T2DM; The studies included a large sample size of participants; And they reported cardiovascular outcomes as their main endpoints. RevMan 5.3 was used to analyze the data, and odds ratios (OR) with 95% confidence intervals (CI) were used to represent the results. RESULTS A total number of 157,478 participants with T2DM were included. Seventy-six thousand and twenty six patients were assigned to the DPP-4 inhibitor group whereas 81,452 patients were assigned to the control group. Results of the current analysis showed that during a mean follow-up time period ranging from 52 to 152 weeks, the primary endpoint (cardiovascular death/non-fatal myocardial infarction (MI)/non-fatal stroke) was not significantly different in the treatment of T2DM patients with versus without DPP-4 inhibitors (OR: 0.95, 95% CI: 0.86-1.04; P = 0.26). Cardiovascular death (OR: 1.00, 95% CI: 0.90-1.10; P = 0.93), stroke (OR: 1.03, 95% CI: 0.89-1.18; P = 0.72), MI (OR: 0.97, 95% CI: 0.88-1.07; P = 0.59), all-cause mortality (OR: 0.84, 95% CI: 0.59-1.18; P = 0.31), hospitalization for cardiovascular complications (OR: 1.02, 95% CI: 0.96-1.09; P = 0.45) and hospitalization specifically for heart failure (OR: 1.05, 95% CI: 0.90-1.23; P = 0.55) were also similarly manifested in both groups. CONCLUSION The current analysis showed that treatment with DPP-4 inhibitors did not significantly increase cardiovascular outcomes in these patients with T2DM indicating that those drugs might be safe to use in terms of cardiovascular events.

中文翻译:

二肽基肽酶4(DPP-4)抑制剂与2型糖尿病(T2DM)患者的心血管结局:系统评价和荟萃分析。

背景技术二肽基肽酶4(DPP-4)抑制剂是较新的口服抗糖尿病药,其已被食品和药物管理局批准用于治疗2型糖尿病(T2DM)患者。在这项分析中,我们旨在系统比较DPP-4抑制剂与非DPP-4抑制剂使用者的心血管结局。方法使用特定术语搜索所有比较DPP-4抑制剂使用情况和报告T2DM患者心血管结局的英文出版物。如果满足以下纳入标准,则将研究包括在内:他们是比较D2DM患者中DPP-4抑制剂使用的随机试验或观察队列/注册机构;这些研究包括大量参与者。他们报告心血管结局为主要终点。使用RevMan 5.3分析数据,并使用具有95%置信区间(CI)的比值比(OR)表示结果。结果包括157,478名T2DM参与者。DPP-4抑制剂组分为76,26例,对照组为81,452例。当前的分析结果表明,在平均随访时间(52至152周)内,治疗的主要终点(心血管死亡/非致命性心肌梗塞(MI)/非致命性中风)无显着差异有或没有DPP-4抑制剂的T2DM患者的比例(OR:0.95,95%CI:0.86-1.04; P = 0.26)。心血管死亡(OR:1.00,95%CI:0.90-1.10; P = 0.93),中风(OR:1.03,95%CI:0.89-1.18; P = 0.72),MI(OR:0.97,95%CI:0.88) -1.07; P = 0.59),全因死亡率(OR:0.84,95%CI:0.59-1.18; P = 0.31),因心血管并发症而住院的患者(OR:1.02,95%CI:0.96-1.09; P = 0.45),以及因心力衰竭而住院的患者( OR:1.05,95%CI:0.90-1.23; P = 0.55)在两组中也相似。结论当前的分析表明,在这些T2DM患者中,用DPP-4抑制剂治疗不会显着增加心血管疾病的预后,表明就心血管事件而言,这些药物可能是安全的。
更新日期:2019-11-01
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