Abstract
Concerns raised by several animal studies, case reports, and pharmacovigilance warnings over incretin-based therapy potentially exposing type two diabetes patients to an elevated risk of pancreatitis have cast a shadow on the overall safety of this class of drugs. This systematic review evaluates the data from observational studies that compared treatment with or without incretins and the risk of pancreatitis. We searched PubMed for publications with the key terms incretins or GLP-1 receptor agonists or DPP-4 inhibitors or sitagliptin or vildagliptin or saxagliptin or linagliptin or alogliptin or exenatide or liraglutide AND pancreatitis in the title or abstract. Studies were evaluated against the following criteria: design (either cohort or case–control); outcome definition (incidence of pancreatitis); exposure definition (new or current or past incretins users); and comparison between patients receiving incretins or not for type 2 diabetes. Two authors independently selected the studies and extracted the data. Six studies meeting the inclusion criteria were reviewed. No difference was found in the overall risk of pancreatitis between incretin users and non-users (odds ratio 1.08; 95 % CI [0.84–1.40]). A risk increase lower than 35 % cannot be excluded according to the power calculation. This systematic review and meta-analysis suggests that type 2 diabetes patients receiving incretin-based therapy are not exposed to an elevated risk of pancreatitis. Limitations of this analysis are the low prevalence of incretin users and the lack of a clear distinction by the studies between therapy with DPP-4 inhibitors or with GLP-1 receptor agonists.
Similar content being viewed by others
References
C.F. Deacon, E. Mannucci, B. Ahre´n, Glycaemic efficacy of glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors as add-on therapy to metformin in subjects with type 2 diabetes-a review and meta analysis. Diabetes. Obes. Metab. 14, 762–767 (2012)
B. Gallwitz, Extra-pancreatic effects of incretin-based therapies. Endocrine (2014). doi:10.1007/s12020-014-0223-0
N. Mikhail, Effects of incretin-based therapy in patients with heart failure and myocardial infarction. Endocrine 47(1), 21–28 (2014). doi:10.1007/s12020-014-0175-4
J.A. Koehler, L.L. Baggio, B.J. Lamont, S.D. Ali, D.J. Drucker, Glucagon-like peptide-1 receptor activation modulates pancreatitis-associated gene expression but does not modify the susceptibility to experimental pancreatitis in mice. Diabetes. 58, 2148–2161 (2009)
J.S. Nachnani, D.G. Bulchandani, A. Nookala, B. Herndon, A. Molteni, P. Pandya, R. Taylor, T. Quinn, L. Weide, L.M. Alba, Biochemical and histological effects of exendin-4 (exenatide) on the rat pancreas. Diabetologia. 53, 153–159 (2010)
K. Tatarkiewicz, P.A. Smith, E.J. Sablan, C.J. Polizzi, D.E. Aumann, C. Villescaz, D.M. Hargrove, B.R. Gedulin, M.G.W. Lu, L. Adams, T. Whisenant, D. Roy, D.G. Parkes, Exenatide does not evoke pancreatitis and attenuates chemically induced pancreatitis in normal and diabetic rodents. Am. J. Physiol. Endocrinol. Metab. 299, E1076–E1086 (2010)
S.N. Iyer, A.J. Drake, R.I. West, C.E. Mendez, R.J. Tanenberg, Case report of acute necrotizing pancreatitis associated with combination treatment of sitagliptin and exenatide. Endocr. Pract. 18, 10–13 (2012)
A.S. Franks, P.H. Lee, C.M. George, Pancreatitis: a potential complication of liraglutide? Ann. Pharmacother. 46, 1547–1553 (2012)
M. Sue, A. Yoshihara, K. Kuboki, N. Hiroi, G. Yoshino, A case of severe acute necrotizing pancreatitis after administration of sitagliptin. Clin. Med. Insights. Case. Rep. 6, 23 (2013)
M. Elashoff, A.V. Matveyenko, B. Gier, R. Elashoff, P.C. Butler, Pancreatitis, pancreatic, and thyroid cancer with glucagon-like peptide-1-based therapies. Gastroenterology. 141, 150–156 (2011)
J.L. Faillie, S. Babai, S. Crépin, V. Bres, M.L. Laroche, H. Le Louet, P. Petit, J.L. Montastruc, D. Hillaire-Buys, The French Pharmacovigilance Centers Network. Pancreatitis associated with the use of GLP-1 analogs and DPP-4 inhibitors: a case/non-case study from the French Pharmacovigilance Database. Acta Diabetol. 51(3), 491–497 (2014)
E.A. Gale, GLP-1 based agents and acute pancreatitis: drug safety falls victim to the three monkey paradigm. BMJ. 346, f1263 (2013)
C.J. Girman, T.D. Kou, B. Cai, C.M. Alexander, E.A. O’Neill, D.E. Williams-Herman, L. Katz, Patients with type 2 diabetes mellitus have higher risk for acute pancreatitis compared with those without diabetes. Diabetes. Obes. Metab. 12, 766–771 (2010)
R.A. Noel, D.K. Braun, R.E. Patterson, G.L. Bloomgren, Increased risk of acute pancreatitis and biliary disease observed in patients with type 2 diabetes: a retrospective cohort study. Diabetes. Care. 32, 834–838 (2009)
A. Gonzalez-Perez, R.G. Schlienger, L.A. Rodríguez, Acute pancreatitis in association with type 2 diabetes and antidiabetic drugs: a population-based cohort study. Diabetes. Care. 33(12), 2580–2585 (2010)
S.-W. Lai, C.-H. Muo, K.-F. Liao, F.-C. Sung, P.-C. Chen, Risk of acute pancreatitis in type 2 diabetes and risk reduction on anti-diabetic drugs: A population-based cohort study in Taiwan. Am. J. Gastroenterol. 106, 1697–1704 (2011)
K.B. Blomgren, A. Sundstrom, G. Steineck, B.E. Wiholm, Obesity and treatment of diabetes with glyburide may both be risk factors for acute pancreatitis. Diabetes. Care. 25, 298–302 (2002)
F.L. Fimognari, A. Corsonello, R. Pastorell, R. Antonelli-Incalzi, Metformin-induced pancreatitis: a possible adverse drug effect during acute renal failure. Diabetes. Care. 29, 1183 (2006)
S. Mallick, Metformin-induced acute pancreatitis precipitated by renal failure. Postgrad. Med. J. 80, 239–240 (2004)
C.B. Giorda, E. Nada, B. Tartaglino, Pharmacokinetics, safety, and efficacy of DPP-4 inhibitors and GLP-1 receptor agonists in patients with type 2 diabetes mellitus and renal or hepatic impairment. A systematic review of the literature. Endocrine 46(3), 406–419 (2014)
M. Monami, I. Dicembrini, E. Mannucci, Dipeptidyl peptidase-4 inhibitors and pancreatitis risk: a meta-analysis of randomized clinical trials. Diabetes. Obes. Metab. 16(1), 48–56 (2014)
B.M. Scirica, D.L. Bhatt, E. Braunwald, P.G. Steg, J. Davidson, P. Hirshberg, R. Frederich, S.D. Wiviott, E.B. Hoffman, M.A. Cavender, J.A. Udell, N.R. Desai, O. Mosenzon, D.K. McGuire, K.K. Ray, L.A. Leiter, I. Raz, the SAVOR-TIMI 53 Steering Committee and Investigators, Saxagliptin and cardiovascular outcomes in patients with type 2 diabetes mellitus. N. Engl. J. Med. 369(14), 1317–1326 (2013)
W.B. White, C.P. Cannon, S.R. Heller, S.E. Nissen, R.M. Bergenstal, G.L. Bakris, A.T. Perez, P.R. Fleck, C.R. Mehta, S. Kupfer, C. Wilson, W.C. Cushman, F. Zannad, the EXAMINE Investigators, Alogliptin after acute coronary syndrome in patients with type 2 diabetes. N. Engl. J. Med. 369(14), 1327–1335 (2013)
L.V. Hedges, T.D. Pigott, The power of statistical test in meta-analysis. Psychol. Methods. 6, 203–217 (2001)
D.D. Dore, M. Hussein, C. Hoffman, E.M. Pelletier, D.B. Smith, J.D. Seeger, A pooled analysis of exenatide use and risk of acute pancreatitis. Curr. Med. Res. Opin. 29(12), 1577–1586 (2013)
D.D. Dore, G.L. Blomgren, M. Wenten et al., A cohort study of acute pancreatitis in relation to exenatide use. Diabetes. Obes. Metab. 13(6), 559–566 (2011)
M. Wenten, J.A. Gaebler, M. Hussein, E.M. Pelletier, D.B. Smith, P. Girase, R.A. Noel, D.K. Braun, G.L. Bloomgren, Relative risk of acute pancreatitis in initiators of exenatide twice daily compared with other anti-diabetic medication: a follow-up study. Diabet. Med. 29(11), 1412–1418 (2012)
D.D. Dore, D. John, J.D. Seeger, Arnold Chan K. Use of a claims-based active drug safety surveillance system to assess the risk of acute pancreatitis with exenatide or sitagliptin compared to metformin or glyburide. Curr. Med. Res. Opin. 25(4), 1019–1027 (2009)
R. Garg, W. Chen, M. Pendergrass, Acute pancreatitis in type 2 diabetes treated with exenatide or sitagliptin: a retrospective observational pharmacy claims analysis. Diabetes. Care. 33(11), 2349–2354 (2010)
J.A. Romley, D.P. Goldman, M. Solomon, D. McFadden, A.L. Peters, Exenatide therapy and the risk of pancreatitis and pancreatic cancer in a privately insured population. Diabetes. Technol. Ther. 14(10), 904–911 (2012)
S. Singh, H.Y. Chang, T.M. Richards, J.P. Weiner, J.M. Clark, J.B. Segal, Glucagon-like peptide 1-based therapies and risk of hospitalization for acute pancreatitis in type 2 diabetes mellitus: a population-based matched case-control study. JAMA. Intern. Med. 173(7), 534–539 (2013)
C.B. Giorda, R. Picariello, E. Nada, B. Tartaglino, L. Marafetti, G. Costa, R. Gnavi, Incretin therapies and risk of hospital admission for acute pancreatitis in an unselected population of European patients with type 2 diabetes: a case-control study. www.thelancet.com/diabetes-endocrinology. Accessed 12 Nov 2013. doi:10.1016/S2213-8587(13)70147-5
M. Monami, I. Iacomelli, N. Marchionni, E. Mannucci, Dipeptidyl peptidase-4 inhibitors in type 2 diabetes: a meta-analysis of randomized clinical trials. Nutr. Metab. Cardiovasc. Dis. 20, 224–235 (2010)
E. Raschi, C. Piccinni, E. Poluzzi, G. Marchesini, F. De Ponti, The association of pancreatitis with antidiabetic drug use: gaining insight through the FDA. Acta Diabetol. 50(4), 569–577 (2013)
M.A. Nauck, J.J. Meier, A critical analysis of the clinical use of incretin-based therapies: the benefits by far outweigh the potential risks. Diabetes. Care. 36, 2126–2132 (2013)
M.A. Nauck, J.J. Meier, Pancreatitis and incretin-based drugs: clarity or confusion? Comment. www.thelancet.com/diabetes-endocrinology. Accessed 12 Nov 2013. doi:10.1016/S2213-8587(13)70186-4
L. Frulloni, C. Lunardi, R. Simone et al., Identification of a novel antibody associated with autoimmune pancreatitis. N. Engl. J. Med. 361, 2135–2142 (2009)
H.M. Lando, M. Alattar, A.P. Dua, Elevated amylase and lipase levels in patients using glucagon-like peptide-1 receptor agonists or dipeptidyful-peptidase-4 inhibitors in the outpatient setting. Endocr. Pract. 18, 472–477 (2012)
Acknowledgments
This study was supported by Chaira Medica Association (non-profit organization for the study of endocrine and metabolic disorders), Chieri, Italy; EN is employed with the Association.
Conflict of interest
CBG discloses teaching and speaking fees from Merck, Novo Nordisk, BMS/AZ Alliance, and BI/Lilly Alliance. All the other authors declare no conflicts of interest.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Giorda, C.B., Sacerdote, C., Nada, E. et al. Incretin-based therapies and acute pancreatitis risk: a systematic review and meta-analysis of observational studies. Endocrine 48, 461–471 (2015). https://doi.org/10.1007/s12020-014-0386-8
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12020-014-0386-8