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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Antiplatelet effects of aspirin in chronic kidney disease patients
A Polzin1, L Dannenberg1, R Sansone1
1Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University Medical Center Dusseldorf, Dusseldorf, Germany.
Insights
Patients with chronic kidney disease (CKD) often experience reduced antiplatelet effects from aspirin, increasing cardiovascular risk. Further research is needed to determine optimal antithrombotic strategies for this population.
Area of Science:
- Cardiovascular Medicine
- Nephrology
- Pharmacology
Background:
- Chronic kidney disease (CKD) patients face elevated cardiovascular event risks.
- Individual responses to aspirin vary, with insufficient antiplatelet effects linked to ischemic events.
- CKD may impact the pharmacodynamic response to antiplatelet drugs, similar to clopidogrel's known effects.
Purpose of the Study:
- To investigate the antiplatelet effects of aspirin in patients diagnosed with CKD.
- To evaluate the relationship between renal function and aspirin's pharmacodynamic response.
Main Methods:
- A cross-sectional study involving 116 patients on long-term aspirin therapy.
- Pharmacodynamic assessment of aspirin's effect using arachidonic acid-induced thromboxane formation.
Main Results:
- High on-treatment platelet reactivity (HTPR) to aspirin was significantly more common in patients with impaired renal function (47% vs. 22%).
- Aspirin's pharmacodynamic response was impaired in moderate/severe CKD patients compared to those with normal/mildly reduced renal function.
- Residual thromboxane formation correlated with glomerular filtration rate, independent of age and gender.
Conclusions:
- Renal function is a key factor influencing the pharmacodynamic response to aspirin.
- CKD patients are at a higher risk of experiencing diminished antiplatelet effects from aspirin.
- Larger trials are necessary to confirm clinical impact and establish optimal antithrombotic regimens for CKD patients.
Unlabelled:
ESSENTIALS: Chronic kidney disease (CKD) patients have a high risk of cardiovascular events. A pharmacodynamic evaluation of the effects of aspirin in 116 patients was carried out. The antiplatelet effects of aspirin are associated with impaired renal function. The optimal antithrombotic regimen in CKD patients must be investigated on a larger scale.
Background:
The pharmacodynamic response to aspirin varies significantly between individuals. Insufficient antiplatelet effects of aspirin are associated with increased risk of ischemic events. Chronic kidney disease (CKD) is suggested to affect the pharmacodynamic response to antiplatelet medication. High on-treatment platelet reactivity (HTPR) to clopidogrel has been reported to partially account for the enhanced risk of death and cardiovascular events in CKD patients. Objective To investigate the antiplatelet effects of aspirin in patients with CKD.
Methods:
We conducted a cross-sectional study in 116 patients on permanent aspirin medication. The pharmacodynamic response to aspirin was determined by arachidonic acid-induced thromboxane formation.
Results:
HTPR to aspirin was more frequent in patients with impaired renal function (47% vs. 22%; odds ratio, 3.16; 95% confidence interval [CI], 1.34-7.41; P = 0.008). The pharmacodynamic response to aspirin was impaired in patients with moderate/severe CKD (92; interquartile range [IQR], 282 ng mL(-1) ) as compared to patients with normal/mildly reduced renal function (36; IQR, 100 ng mL(-1) ; difference in medians, 57; CI, 5-110 ng mL(-1) ; P = 0.013). Bivariate Pearson analysis showed residual thromboxane formation to be correlated with glomerular filtration rate (R = -0.303; R(2) = 0.092; P = 0.001). Patients with CKD were older and more frequently female. Multivariate linear regression analysis revealed that the correlation was independent of age (R = -0.314; R(2) = 0.082; P = 0.002) and gender (R = -0.305; R(2) = 0.077; P = 0.006).
Conclusion:
Renal function is correlated with pharmacodynamic response to aspirin. Patients with CKD have an increased risk of impaired antiplatelet effects of aspirin. Larger trials are needed to assess the clinical impact of this finding and investigate the optimal antithrombotic regimen in CKD patients.
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