Title The cardiovascular effect of incretin-based therapies among type 2 diabetes: a systematic review and network meta-analysis
Authors Wu, Shanshan
Cipriani, Andrea
Yang, Zhirong
Yang, Jun
Cai, Ting
Xu, Yang
Quan, Xiaochi
Zhang, Yuan
Chai, Sanbao
Sun, Feng
Zhan, Siyan
Affiliation Capital Med Univ, Beijing Friendship Hosp, Natl Clin Res Ctr Digest Dis, Beijing, Peoples R China.
Univ Oxford, Dept Psychiat, Oxford, England.
Warneford Hosp, Oxford Hlth NHS Fdn Trust, Oxford, England.
Univ Cambridge, Sch Clin Med, Dept Publ Hlth & Primary Care, Primary Care Unit, Cambridge, England.
Peking Univ, Hlth Sci Ctr, Sch Publ Hlth, Dept Epidemiol & Biostat, Beijing, Peoples R China.
McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON, Canada.
Peking Univ, Int Hosp, Dept Endocrinol & Metab, Beijing, Peoples R China.
Harvard Med Sch, Dept Populat Med, Boston, MA USA.
Peking Univ, Hlth Sci Ctr, Sch Publ Hlth, Dept Epidemiol & Biostat, Beijing, Peoples R China.
Sun, F (reprint author), Harvard Med Sch, Dept Populat Med, Boston, MA USA.
Keywords Incretin-based therapies
type 2 diabetes
network meta-analysis
cardiovascular effect
DIPEPTIDYL PEPTIDASE-4 INHIBITORS
PEPTIDE-1 RECEPTOR AGONISTS
RANDOMIZED CLINICAL-TRIALS
LEVEL POOLED ANALYSIS
GLYCEMIC CONTROL
HEART-FAILURE
DOUBLE-BLIND
FOLLOW-UP
OUTCOMES
SAFETY
Issue Date 2018
Publisher EXPERT OPINION ON DRUG SAFETY
Citation EXPERT OPINION ON DRUG SAFETY. 2018, 17(3), 243-249.
Abstract Objective: To evaluate the comparative cardiovascular safety of incretin-based therapies in patients with type 2 diabetes mellitus (T2DM). Methods: Medline, Embase, the Cochrane Library and www.clinicaltrials.gov were searched for randomized controlled trials (RCTs) with duration >= 12 weeks. Network meta-analysis was performed, followed by subgroup analysis and meta-regression. The Grading of Recommendations Assessment, Development and Evaluation system was used to assess the quality of evidence. The outcome of interest was a composite of cardiovascular death, myocardial infarction, stroke and heart failure. Odds ratio (OR) with 95% confidence interval (CI) was calculated as the measure of effect size. Results: 281 RCTs (76.9% double-blinded) with 180,000 patients were included, comparing incretin-based therapies with other six classes of anti-diabetic drugs or placebo. A statistically significant reduction in the risk of cardiovascular events was found in favour of GLP-1RAs when compared with placebo (OR 0.89, 95%CI: 0.80-0.99) and sulfonylurea (OR 0.76, 95%CI: 0.59-0.99), whereas DPP-4 inhibitors showed a neutral effect compared with placebo (OR 0.92, 95%CI: 0.83-1.01). Conclusions: Incretin-based therapies show similar cardiovascular risk in comparison with metformin, insulin, thiazolidinediones, alpha-glucosidase inhibitor and sodium-glucose co-transporter 2. GLP-1RA could decrease the risk compared with sulfonylurea or placebo, while DPP-4I appears to have neutral effect on cardiovascular risk.
URI http://hdl.handle.net/20.500.11897/502488
ISSN 1474-0338
DOI 10.1080/14740338.2018.1424826
Indexed SCI(E)
PubMed
Appears in Collections: 公共卫生学院
国际医院

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