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Published on: May 14, 2013
Statin use and incident cardiovascular events in renal transplant recipients
Josephine L C Anderson1, Markus van der Giet2, Antonio W Gomes Neto1
1Department of Internal Medicine, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Insights
Statins did not significantly reduce cardiovascular events in renal transplant recipients. However, in those also taking cyclosporine, statins were linked to increased cardiovascular events and mortality, possibly due to drug interactions.
Area of Science:
- Nephrology
- Cardiology
- Pharmacology
Background:
- Statins effectively reduce cardiovascular risk in the general population.
- Guidelines recommend statins for renal transplant recipients (RTR).
- Evidence for statin benefit in RTR is inconsistent, with concerns about cyclosporine interactions.
Purpose of the Study:
- To evaluate the effect of statins on cardiovascular outcomes in RTR.
- To specifically analyze outcomes in RTR using cyclosporine.
Main Methods:
- Propensity score matching was used to compare 622 RTR with and without statin use.
- Follow-up was 5.4 years.
- Survival analysis, including Cox regression, was performed.
Main Results:
- Statin use was not significantly associated with a composite cardiovascular endpoint in the overall RTR cohort (HR=0.81, P=0.33).
- In RTR using cyclosporine, statin use showed a significant positive association with the composite cardiovascular outcome (HR=6.60, P=0.005).
- Statin use correlated positively with cyclosporine trough levels (r=0.11, P=0.04).
Conclusions:
- Statin use does not significantly reduce cardiovascular events in the overall RTR population.
- Statin use is independently associated with increased cardiovascular events and mortality in RTR taking cyclosporine.
- A potential drug interaction between statins and cyclosporine may explain these findings.
Background:
Statins achieve potent LDL lowering in the general population leading to a significant cardiovascular (CV) risk reduction. In renal transplant recipients (RTR) statins are included in treatment guidelines, however, conclusive evidence of improved cardiovascular outcomes has not been uniformly provided and concerns have been raised about simultaneous use of statins and the immunosuppressant cyclosporine. This study aimed to elucidate the effect of statins on a compound CV endpoint, comprised of ischaemic CV events and CV mortality in RTR, with subgroup analysis focussing on cyclosporine users.
Method:
622 included RTR (follow-up 5.4 years) were matched based on propensity scores and dichotomized by statin use. Survival analysis was conducted.
Results:
Cox regression showed that statin use was not significantly associated with the compound CV endpoint in a fully adjusted model (HR = 0.81, 95% CI = 0.53-1.24, P = .33). Subgroup analyses in RTR using cyclosporine revealed a strong positive association of statin use with the CV compound outcome in a fully adjusted model (HR = 6.60, 95% CI 1.75-24.9, P = .005). Furthermore, statin use was positively correlated with cyclosporine trough levels (correlation coefficient 0.11, P = .04).
Conclusion:
In conclusion, statin use does not significantly decrease incident CV events in an overall RTR cohort, but is independently associated with CV-specific mortality and events in cyclosporine using RTR, possibly due to a bilateral pharmacological interaction.
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