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Published on: March 29, 2019
Diabetes Pharmacotherapies and Bladder Cancer: A Medicare Epidemiologic Study
Todd A Mackenzie1, Rebecca Zaha2, Jeremy Smith2
1Section of Clinical Research, HB 7505, Dartmouth-Hitchcock Medical Center, One Medical Center Drive, Lebanon, NH, 03756, USA. todd.a.mackenzie@dartmouth.edu.
Objective:
Patients with type II diabetes have an increased risk of bladder cancer and are commonly treated with thiazolidinediones and angiotensin receptor blockers (ARBs), which have been linked to cancer risk. We explored the relationship between use of one or both of these medication types and incident bladder cancer among diabetic patients (diabetics) enrolled in Medicare.
Research Design And Methods:
We constructed both a prevalent and incident retrospective cohort of pharmacologically treated prevalent diabetics enrolled in a Medicare fee-for-service plan using inpatient, outpatient (2003-2011) and prescription (2006-2011) administrative data. The association of incident bladder cancer with exposure to pioglitazone, rosiglitazone and ARBs was studied using muitivariable Cox's hazard models with time-dependent covariates in each of the two cohorts.
Results:
We identified 1,161,443 prevalent and 320,090 incident pharmacologically treated diabetics, among whom 4433 and 1159, respectively, developed incident bladder cancers. In the prevalent cohort mean age was 75.1 years, mean follow-up time was 38.0 months, 20.2% filled a prescription for pioglitazone during follow-up, 10.4% received rosiglitazone, 31.6% received an ARB and 8.0% received combined therapy with pioglitazone + ARB. We found a positive association between bladder cancer and duration of pioglitazone use in the prevalent cohort (P for trend = 0.008), with ≥24 months of pioglitazone exposure corresponding to a 16% (95% confidence interval 0-35%) increase in the incidence of bladder cancer compared to no use. There was a positive association between bladder cancer and rosiglitazone use for <24 months in the prevalent cohort, but no association with ARB use. There were no significant associations in the incident cohort.
Conclusions:
We found that the incidence of bladder cancer increased with duration of pioglitazone use in a prevalent cohort of diabetics aged 65+ years residing in the USA, but not an incident cohort.
Insights
Long-term pioglitazone use in diabetic patients aged 65+ was associated with an increased risk of bladder cancer. This finding highlights potential medication risks in diabetes management and warrants further investigation into drug safety.
Area of Science:
- Endocrinology
- Oncology
- Pharmacoepidemiology
Background:
- Type II diabetes is linked to an elevated risk of bladder cancer.
- Common diabetes medications, thiazolidinediones and angiotensin receptor blockers (ARBs), have been investigated for potential cancer risks.
Purpose of the Study:
- To investigate the association between the use of thiazolidinediones (pioglitazone, rosiglitazone) and ARBs and the incidence of bladder cancer in diabetic patients.
- To analyze medication use in a large cohort of diabetic patients enrolled in Medicare.
Main Methods:
- Retrospective cohort study using Medicare administrative data (2003-2011).
- Inclusion of prevalent and incident cohorts of pharmacologically treated diabetics.
- Multivariable Cox's hazard models with time-dependent covariates were employed to assess associations.
Main Results:
- A positive association was observed between longer duration of pioglitazone use (≥24 months) and increased bladder cancer incidence in the prevalent cohort (16% increase).
- A positive association was found between rosiglitazone use (<24 months) and bladder cancer in the prevalent cohort.
- No significant associations were found between ARB use and bladder cancer, nor in the incident cohort.
Conclusions:
- Increased duration of pioglitazone use is associated with a higher incidence of bladder cancer in older diabetic patients.
- The findings suggest a potential link between specific diabetes medications and bladder cancer risk, particularly with prolonged pioglitazone exposure.
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