Article date: December 2015
By: Maria E. Goossens, Frank Buntinx, Maurice P. Zeegers, J.H.M. Driessen, Marie L. De Bruin, Frank De Vries in Volume 80, Issue 6, pages 1464-1472
Aim
The aim of this study was to look at the influence of metformin intake and duration, on urinary bladder cancer (UBC) risk, with sulfonylurea (SU) only users as control using a new user design (inception cohort).
Methods
We conducted a retrospective cohort study using data from the UK Clinical Practice Research Datalink (CPRD) including all patients with at least one prescription of oral anti‐diabetic drugs (ADD) and/or insulin. The risk of UBC in different groups of ADD users (metformin alone (one), metformin in combination (two) with other ADD medication (glinides, glitazones, DPP‐4‐inhibitors, SUs, insulin or more than one combination), all metformin users (1 + 2) was compared with SU only users using Cox proportional hazards models. The estimates were adjusted for age, gender, smoking status, BMI and diabetes duration.
Results
The inception cohort included 165 398 participants of whom 132 960 were metformin users and 32 438 were SU only users. During a mean follow‐up time of more than 5 years 693 patients developed UBC, 124 of the control group and 461 of the all metformin users. There was no association between metformin use and UBC risk (HR = 1.12, 95% CI 0.90, 1.40) compared with SU only users, even after adjustment for diabetes duration (HR = 1.13, 95% CI 0.90, 1.40). We found a pattern of decreasing risk of UBC with increasing duration of metformin intake, which was statistically not significant.
Conclusion
Metformin has no influence on the risk of UBC compared with SU in type 2 diabetes patients using a new user design.
DOI: 10.1111/bcp.12740
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