Skip to main content

Advertisement

Log in

Effects of exenatide long-acting release on cardiovascular events and mortality in patients with type 2 diabetes: a systematic review and meta-analysis of randomized controlled trials

  • Original Article
  • Published:
Acta Diabetologica Aims and scope Submit manuscript

Abstract

Aims

Patients with type 2 diabetes (T2D) have an increased risk of cardiovascular disease. Recent cardiovascular outcome trials (CVOTs) with liraglutide, semaglutide, and albiglutide have shown significant reduction in major adverse cardiovascular events. Conversely, the CVOT with exenatide long-acting release (ELAR) confirmed cardiovascular safety of the drug, but did not reached superiority versus placebo. Herein, we systematically evaluated the effect of ELAR versus placebo or active comparators on cardiovascular events and mortality in patients with T2D.

Methods

We screened the literature for randomized controlled trials reporting cardiovascular events and deaths in patients receiving ELAR versus those receiving placebo or any other glucose-lowering medications. Event rates were pooled and compared using the random-effects model.

Result

We retrieved 16 trials comparing the occurrence of cardiovascular events and mortality in patients treated with ELAR versus placebo or active comparators. The pooled rate ratio for cardiovascular events was similar in the two groups (0.99; 95% CI 0.92–1.06). The rate ratio for all-cause mortality was significantly lower in exenatide group than in comparators (0.87; 95% CI 0.77–0.97). When results of the EXSCEL trial were omitted, the pooled rate ratio for cardiovascular events and mortality was 0.80 (95% CI 0.40–1.63) and 0.75 (95% CI 0.30–1.84), respectively.

Conclusions

Treatment with ELAR does not increase the risk of cardiovascular events and may reduce all-cause mortality.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Sarwar N, Gao P, Kondapally Seshasai SR et al (2010) Diabetes mellitus, fasting blood glucose concentration, and risk of vascular disease: a collaborative meta-analysis of 102 prospective studies. Lancet 375(9733):2215–2222

    Article  CAS  Google Scholar 

  2. Kondapally Seshasai SR, Kaptoge S, Thompson A et al (2011) Diabetes mellitus, fasting glucose, and risk of cause-specific death. N Engl J Med. 364(9):829–841

    Article  Google Scholar 

  3. Zoungas S, Arima H, Gerstein HC et al (2017) Effects of intensive glucose control on microvascular outcomes in patients with type 2 diabetes: a meta-analysis of individual participant data from randomised controlled trials. Lancet Diabetes Endocrinol 5(6):431–437

    Article  Google Scholar 

  4. Holman RR, Paul SK, Bethel MA, Matthews DR, Neil HAW (2008) 10-year follow-up of intensive glucose control in type 2 diabetes. N Engl J Med 359(15):1577–1589

    Article  CAS  Google Scholar 

  5. Uni- M, Sciences HH, Miller ME et al (2011) Long-term effects of intensive glucose lowering on cardiovascular outcomes. N Engl J Med 364(9):818–828

    Article  Google Scholar 

  6. Nissen SE, Wolski K (2007) Effect of rosiglitazone on the risk of myocardial infarction and death from cardiovascular causes. N Engl J Med 356(24):2457–2471

    Article  CAS  Google Scholar 

  7. Petrie JR (2013) The cardiovascular safety of incretin-based therapies: a review of the evidence. Cardiovasc Diabetol 12(1):130

    Article  Google Scholar 

  8. Pfeffer MA, Claggett B, Diaz R et al (2015) Lixisenatide in patients with type 2 diabetes and acute coronary syndrome. N Engl J Med 373(23):2247–2257

    Article  CAS  Google Scholar 

  9. Jones B (2016) Liraglutide and cardiovascular outcomes in type 2 diabetes. Ann Clin Biochem 53(6):712

    Article  Google Scholar 

  10. Marso SP, Bain SC, Consoli A et al (2016) Semaglutide and cardiovascular outcomes in patients with type 2 diabetes. N Engl J Med 375(19):1834–1844

    Article  CAS  Google Scholar 

  11. Hernandez AF, Green JB, Janmohamed S et al (2018) Albiglutide and cardiovascular outcomes in patients with type 2 diabetes and cardiovascular disease (Harmony Outcomes): a double-blind, randomised placebo-controlled trial. Lancet 392(10157):1519–1529

    Article  CAS  Google Scholar 

  12. Holman RR, Bethel MA, Mentz RJ et al (2017) Effects of once-weekly exenatide on cardiovascular outcomes in type 2 diabetes. N Engl J Med 377(13):1228–1239

    Article  CAS  Google Scholar 

  13. Moher D, Liberati A, Tetzlaff J, Altman DG (2009) Preferred reporting items for systematic reviews and meta-analyses: the prisma statement. Ann Intern Med. 151(4):264–269

    Article  Google Scholar 

  14. Higgins JPT, Altman DG, Gøtzsche PC et al (2011) The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ 18(343):d5928

    Article  Google Scholar 

  15. Kunz LM, Normand S-LT, Sedrakyan A (2015) Meta-analysis of rate ratios with differential follow-up by treatment arm: inferring comparative effectiveness of medical devices. Stat Med 34(21):2913–2925

    Article  Google Scholar 

  16. Newman JD, Vani AK, Aleman JO, Weintraub HS, Berger JS, Schwartzbard AZ (2018) The changing landscape of diabetes therapy for cardiovascular risk reduction: JACC state-of-the-art review. J Am Coll Cardiol 72(15):1856–1869

    Article  Google Scholar 

  17. Hernandez AF, Green JB, Janmohamed S et al (2018) Albiglutide and cardiovascular outcomes in patients with type 2 diabetes and cardiovascular disease (Harmony Outcomes): a double-blind, randomised placebo-controlled trial. Lancet. 392(10157):1519–1529

    Article  CAS  Google Scholar 

  18. Walter SD (1991) Statistical significance and fragility criteria for assessing a difference of two proportions. J Clin Epidemiol. 44(12):1373–1378

    Article  CAS  Google Scholar 

  19. Meier JJ (2012) GLP-1 receptor agonists for individualized treatment of type 2 diabetes mellitus. Nat Rev Endocrinol. 8:728

    Article  CAS  Google Scholar 

  20. Lund A, Knop FK, Vilsbøll T (2014) Glucagon-like peptide-1 receptor agonists for the treatment of type 2 diabetes: differences and similarities. Eur J Intern Med 25(5):407–414

    Article  CAS  Google Scholar 

  21. Gerstein HC, Colhoun HM, Dagenais GR et al (2018) Design and baseline characteristics of participants in the Researching cardiovascular events with a weekly incretin in diabetes (REWIND) trial on the cardiovascular effects of dulaglutide. Diabetes Obes Metab 20(1):42–49

    Article  CAS  Google Scholar 

  22. Bain SC, Mosenzon O, Arechavaleta R et al (2018) Cardiovascular safety of oral semaglutide in patients with type 2 diabetes: rationale, design and patient baseline characteristics for the PIONEER 6 trial. Diabetes Obes Metab 21(3):499–508

    Article  Google Scholar 

  23. A study to evaluate cardiovascular outcomes in patients with type 2 diabetes treated with ITCA 650. https://clinicaltrials.gov/ct2/show/NCT01455896. Accessed 21 Jan 2019

  24. Trulicity® (dulaglutide) demonstrates superiority in reduction of cardiovascular events for broad range of people with type 2 diabetes, pp 1–3, (2018). https://investor.lilly.com/node/39796/pdf. Accessed 21 Jan 2019

  25. IDF (2017) International diabetes federation. IDF Diabetes Atlas, 8th edn. Brussels, Belgium, International Diabetes Federation, pp 1–150. http://www.diabetesatlas.org. Accessed 21 Jan 2019

  26. Buse JB, Nauck M, Forst T et al (2013) Exenatide once weekly versus liraglutide once daily in patients with type 2 diabetes (DURATION-6): a randomised, open-label study. Lancet 381(9861):117–124

    Article  CAS  Google Scholar 

  27. Jabbour SA, Frías JP, Hardy E et al (2018) Safety and efficacy of exenatide once weekly plus dapagliflozin once daily versus exenatide or dapagliflozin alone in patients with type 2 diabetes inadequately controlled with metformin monotherapy: 52-week results of the DURATION-8 randomized controlled. Diabetes Care 41(10):2136–2146

    Article  CAS  Google Scholar 

  28. Ahmann AJ, Capehorn M, Charpentier G et al (2018) Efficacy and safety of once-weekly semaglutide versus exenatide ER in subjects with type 2 diabetes (SUSTAIN 3): a 56-week, open-label, randomized clinical trial. Diabetes Care 41(2):258–266

    Article  CAS  Google Scholar 

  29. Drucker DJ, Buse JB, Taylor K et al (2008) Exenatide once weekly versus twice daily for the treatment of type 2 diabetes: a randomised, open-label, non-inferiority study. Lancet 372(9645):1240–1250

    Article  CAS  Google Scholar 

  30. Bergenstal RM, Wysham C, MacConell L et al (2010) Efficacy and safety of exenatide once weekly versus sitagliptin or pioglitazone as an adjunct to metformin for treatment of type 2 diabetes (DURATION-2): a randomised trial. Lancet 376(9739):431–439

    Article  Google Scholar 

  31. Diamant M, Van Gaal L, Stranks S et al (2010) Once weekly exenatide compared with insulin glargine titrated to target in patients with type 2 diabetes (DURATION-3): an open-label randomised trial. Lancet 375(9733):2234–2243

    Article  CAS  Google Scholar 

  32. Russell-Jones D, Cuddihy RM, Hanefeld M et al (2012) Efficacy and safety of exenatide once weekly versus metformin, pioglitazone, and sitagliptin used as monotherapy in drug-naive patients with type 2 diabetes (DURATION-4). Diabetes Care 35(2):252–258

    Article  CAS  Google Scholar 

  33. Blevins T, Pullman J, Malloy J et al (2011) DURATION-5: exenatide once weekly resulted in greater improvements in glycemic control compared with exenatide twice daily in patients with type 2 diabetes. J Clin Endocrinol Metab 96(5):1301–1310

    Article  CAS  Google Scholar 

  34. Guja C, Frías JP, Somogyi A et al (2018) Effect of exenatide QW or placebo, both added to titrated insulin glargine, in uncontrolled type 2 diabetes: the DURATION-7 randomized study. Diabetes Obes Metab 20:1602–1614

    Article  CAS  Google Scholar 

  35. Wysham CH, Rosenstock J, Vetter ML (2018) Efficacy and tolerability of the new autoinjected suspension of exenatide once weekly versus exenatide twice daily in patients with type 2 diabetes. Diabetes Obes Metab 20(1):165–172

    Article  CAS  Google Scholar 

  36. Gadde KM, Vetter ML, Iqbal N, Hardy E, Öhman P (2017) Efficacy and safety of autoinjected exenatide once-weekly suspension versus sitagliptin or placebo with metformin in patients with type 2 diabetes: the DURATION-NEO-2 randomized clinical study. Diabetes Obes Metab 19(7):979–988

    Article  CAS  Google Scholar 

  37. Davies M, Heller S, Sreenan S et al (2013) Once-weekly exenatide versus once- or twice-daily insulin detemir, (5 CC-Metabolic and Endocrine Disorders). Diabetes Care. 36:1368–1376

    Article  CAS  Google Scholar 

  38. Inagaki N, Atsumi Y, Oura T, Saito H, Imaoka T (2012) Efficacy and safety profile of exenatide once weekly compared with insulin once daily in japanese patients with type 2 diabetes treated with oral antidiabetes drug(s): results from a 26-week, randomized, open-label, parallel-group, multicenter. Noninferio Clin Ther. 34(9):1892–1908.e1

    Article  CAS  Google Scholar 

  39. Ji L, Onishi Y, Ahn CW et al (2013) Efficacy and safety of exenatide once-weekly vs exenatide twice-daily in Asian patients with type 2 diabetes mellitus. J Diabetes Investig 4(1):53–61

    Article  CAS  Google Scholar 

  40. Abdul-Ghani M, Migahid O, Megahed A, Adams J, Triplitt C, DeFronzo RA et al (2017) Combination therapy with exenatide plus pioglitazone versus basal/bolus insulin in patients with poorly controlled type 2 diabetes on sulfonylurea plus metformin: the qatar study. Diabetes Care 40(3):325–331

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to G. P. Fadini.

Ethics declarations

Conflict of interest

GPF received grant support, lecture, or advisory board fees from AstraZeneca, Boehringer-Ingelheim, Eli Lilly, NovoNordisk, Sanofi, Genzyme, Abbott, Novartis, Merck Sharp & Dohme. BMB received lecture or advisory board fees from Novartis, Eli Lilly, AstraZeneca, and Boehringer-Ingelheim. AA received research grants, lecture, or advisory board fees from Merck Sharp & Dome, AstraZeneca, Novartis, Boehringher-Ingelheim, Sanofi, Mediolanum, Janssen, NovoNordisk.

Ethical approval

Not applicable.

Informed consent

Not applicable.

Additional information

Managed by Massimo Federici.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOCX 130 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bonora, B.M., Avogaro, A. & Fadini, G.P. Effects of exenatide long-acting release on cardiovascular events and mortality in patients with type 2 diabetes: a systematic review and meta-analysis of randomized controlled trials. Acta Diabetol 56, 1051–1060 (2019). https://doi.org/10.1007/s00592-019-01347-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00592-019-01347-0

Keywords

Navigation