Influence of metformin intake on the risk of bladder cancer in type 2 diabetes patients

被引:23
作者
Goossens, Maria E. [1 ]
Buntinx, Frank [1 ,2 ]
Zeegers, Maurice P. [3 ]
Driessen, J. H. M. [4 ,5 ,6 ]
De Bruin, Marie L. [4 ]
de Vries, Frank [4 ,5 ,6 ,7 ]
机构
[1] Katholieke Univ Leuven, Dept Gen Practice, Leuven, Belgium
[2] Maastricht Univ, Dept Gen Practice, NL-6200 MD Maastricht, Netherlands
[3] Maastricht Univ, NUTRIM Sch Nutr Metab & Toxicol, NL-6200 MD Maastricht, Netherlands
[4] Univ Utrecht, Div Pharmacoepidemiol & Clin Pharmacol, Utrecht Inst Pharmaceut Sci, NL-3508 TC Utrecht, Netherlands
[5] Maastricht Univ, Med Ctr, Dept Clin Pharm & Toxicol, NL-6200 MD Maastricht, Netherlands
[6] Maastricht Univ, Res Inst CAPHRI, NL-6200 MD Maastricht, Netherlands
[7] Univ Southampton, MRC, Lifecourse Epidemiol Unit, Southampton, Hants, England
关键词
bladder cancer; metformin; type 2 diabetes mellitus; MELLITUS; PROLIFERATION; PREVENTION; MORTALITY; OUTCOMES; PEOPLE; CELLS;
D O I
10.1111/bcp.12740
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:1464 / 1472
页数:9
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