Acute Pancreatitis in Type 2 Diabetes Treated With Exenatide or Sitagliptin

被引:254
作者
Garg, Rajesh [2 ]
Chen, William [1 ]
Pendergrass, Merri [1 ,3 ]
机构
[1] Medco Hlth Solut, Franklin Lakes, NJ USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Boston, MA 02115 USA
[3] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
关键词
RISK;
D O I
10.2337/dc10-0482
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE- Cases of acute pancreatitis have been reported in association with exenatide, sitagliptin, and type 2 diabetes without use of these medications. It remains unknown whether exenatide or sitagliptin increase the risk of acute pancreatitis. RESEARCH DESIGN AND METHODS- A retrospective cohort study of a large medical and pharmacy claims database was performed. Data for 786,656 patients were analyzed. Cox proportional hazard models were built to compare the risk of acute pancreatitis between diabetic and nondiabetic subjects and between exenatide, sitagliptin, and control diabetes medication use. RESULTS- Incidence of acute pancreatitis in the nondiabetic control group, diabetic control group, exenatide group, and sitagliptin group was 1.9, 5.6, 5.7, and 5.6 cases per 1,000 patient years, respectively. The risk of acute pancreatitis was significantly higher in the combined diabetic groups than in the nondiabetic control group (adjusted hazard ratio 2.11 [95% CI 1.7-2.5]). Risk of acute pancreatitis was similar in the exenatide versus diabetic control group (0.9 [0.6-1.5]) and sitagliptin versus diabetic control group (1.0 [0.7-1.3]). CONCLUSIONS- Our study demonstrated increased incidence of acute pancreatitis in diabetic versus nondiabetic patients but did not find an association between the use of exenatide or sitagliptin and acute pancreatitis. The limitations of this observational claims-based analysis cannot exclude the possibility of an increased risk.
引用
收藏
页码:2349 / 2354
页数:6
相关论文
共 14 条
[1]
Ahmad SR, 2008, NEW ENGL J MED, V358, P1970
[2]
[Anonymous], 2008, Information for Healthcare Professionals: Conventional Antipsychotics
[3]
[Anonymous], SITAGLIPTIN MARKETED
[4]
EXENATIDE-INDUCED ACUTE PANCREATITIS [J].
Ayoub, Walaa A. ;
Kumar, Ashok A. ;
Naguib, Hossam S. ;
Taylor, Harris C. .
ENDOCRINE PRACTICE, 2010, 16 (01) :80-83
[5]
GLP-1-Based Therapy for Diabetes: What You Do Not Know Can Hurt You [J].
Butler, Peter C. ;
Dry, Sarah ;
Elashoff, Robert .
DIABETES CARE, 2010, 33 (02) :453-455
[6]
Exenatide (Exendin-4)-induced pancreatitis - A case report [J].
Denker, PS ;
Dimarco, PE .
DIABETES CARE, 2006, 29 (02) :471-471
[7]
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 [J].
Dore, David D. ;
Seeger, John D. ;
Chan, K. Arnold .
CURRENT MEDICAL RESEARCH AND OPINION, 2009, 25 (04) :1019-1027
[8]
Patients with type 2 diabetes mellitus have higher risk for acute pancreatitis compared with those without diabetes [J].
Girman, C. J. ;
Kou, T. D. ;
Cai, B. ;
Alexander, C. M. ;
O'Neill, E. A. ;
Williams-Herman, D. E. ;
Katz, L. .
DIABETES OBESITY & METABOLISM, 2010, 12 (09) :766-771
[9]
Matveyenko AV, 2009, DIABETES, V58, pA412
[10]
Biochemical and histological effects of exendin-4 (exenatide) on the rat pancreas [J].
Nachnani, J. S. ;
Bulchandani, D. G. ;
Nookala, A. ;
Herndon, B. ;
Molteni, A. ;
Pandya, P. ;
Taylor, R. ;
Quinn, T. ;
Weide, L. ;
Alba, L. M. .
DIABETOLOGIA, 2010, 53 (01) :153-159