Abstract
Background: Incretins are new therapeutic agents for the treatment of Type 2 Diabetes Mellitus (T2DM), and are a subgroup of the Non-Insulin Antidiabetic Drugs (NIAD). Although incretin agents have demonstrated efficacy for T2DM, they have been associated with pancreatitis. Recent literature shows limited and conflicting evidence for the association between incretin agents and the risk of acute pancreatitis. Furthermore, the risk of chronic pancreatitis with the use of incretin agents has not been investigated. Objectives: To determine the association between the use of incretin agents and the risk of acute and chronic pancreatitis. Methods: A retrospective population based cohort study, using data from the Clinical Practice Research Datalink (CPRD) (2007.2012), was conducted. Patients (N=182,428) with at least one NIAD prescription and aged 18+ during data collection, were matched to one control patient without diabetes. Multivariable Cox proportional hazards models and a new user design were used to estimate the hazard ratio of (acute, chronic and any) pancreatitis in incretin users (N=28,370) compared with non-diabetics and other NIAD-treated patients. Time dependent adjustments were made for age, sex, life style, comorbidities and drug use. Results: Current NIAD use was associated with acute, chronic and any pancreatitis. This risk increased among current incretin users, as compared to non-diabetic controls. However, only any pancreatitis was associated with incretin use when compared to other NIAD-treated patients (HR=1.47, 95% CI 1.06.2.04). Pancreatitis risk was higher among younger patients (age 18-≥59 years), those with a BMI
Original language | English |
---|---|
Pages (from-to) | 246 |
Number of pages | 1 |
Journal | Pharmacoepidemiology and Drug Safety |
Volume | 25 |
DOIs | |
Publication status | Published - 1 Aug 2016 |
Event | 32nd International conference on Pharmacoepidemiology & Therapeutic Risk Management - The convention centre Dublin, Dublin, Ireland Duration: 25 Aug 2016 → 28 Aug 2016 |
Keywords
- antidiabetic agent
- endogenous compound
- incretin
- acute pancreatitis
- adult
- body mass
- chronic pancreatitis
- clinical practice
- clinical trial
- cohort analysis
- comorbidity
- consensus development
- controlled study
- diabetic patient
- drug therapy
- hazard ratio
- human
- information processing
- lifestyle
- major clinical study
- non insulin dependent diabetes mellitus
- population based case control study
- prescription
- proportional hazards model
- young adult