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Platelet Function in CKD: A Systematic Review and Meta-Analysis
Constance C F M J Baaten1,2, Marieke Sternkopf1, Tobias Henning1
1Institute for Molecular Cardiovascular Research, University Hospital Aachen, Rheinisch-Westfälische Technische Hochschule Aachen University, Aachen, Germany.
Insights
Patients with chronic kidney disease (CKD) exhibit varied platelet function, often impaired, increasing risks for bleeding and clotting. Further research into CKD
Area of Science:
- Nephrology
- Hematology
- Thrombosis Research
Background:
- Chronic kidney disease (CKD) patients face high risks of thrombotic and hemorrhagic events.
- Platelet function abnormalities are key to these complications, with conflicting reports on reactivity in CKD.
- Uremic toxins' direct effects on platelet function are inconsistently described.
Purpose of the Study:
- To systematically review and meta-analyze platelet activity in CKD, focusing on non-dialysis effects.
- To investigate the impact of individual uremic toxins on platelet function through literature review.
Main Methods:
- Systematic review of 73 studies assessing overall platelet function in CKD patients.
- Meta-analysis of 11 studies on ex vivo platelet aggregation in CKD.
- Literature search for uremic toxin effects on platelet function.
Main Results:
- Most studies indicate impaired platelet function in CKD, with prolonged bleeding time and reduced adhesion.
- Meta-analysis shows significantly reduced maximal platelet aggregation in CKD patients upon collagen stimulation.
- Ex vivo studies on uremic toxins yielded variable results; animal models suggest prothrombotic effects.
Conclusions:
- While most studies report impaired platelet function in CKD, some find it unchanged or enhanced.
- Further investigation into platelet reactivity across different CKD stages is necessary.
- Understanding these complex platelet alterations is crucial for managing CKD complications.
Background:
Patients with CKD are at high risk for thrombotic and hemorrhagic complications. Abnormalities in platelet function are central to these complications, but reports on platelet function in relation to CKD are conflicting, and vary from decreased platelet reactivity to normal or increased platelet responsiveness. The direct effects of uremic toxins on platelet function have been described, with variable findings.
Methods:
To help clarify how CKD affects platelet function, we conducted a systematic review and meta-analysis of platelet activity in CKD, with a focus on nondialysis-induced effects. We also performed an extensive literature search for the effects of individual uremic toxins on platelet function.
Results:
We included 73 studies in the systematic review to assess CKD's overall effect on platelet function in patients; 11 of them described CKD's effect on ex vivo platelet aggregation and were included in the meta-analysis. Although findings on platelet abnormalities in CKD are inconsistent, bleeding time was mostly prolonged and platelet adhesion mainly reduced. Also, the meta-analysis revealed maximal platelet aggregation was significantly reduced in patients with CKD upon collagen stimulation. We also found that relatively few uremic toxins have been examined for direct effects on platelets ex vivo; ex vivo analyses had varying methods and results, revealing both platelet-stimulatory and inhibitory effects. However, eight of the 12 uremic toxins tested in animal models mostly induced prothrombotic effects.
Conclusions:
Overall, most studies report impaired function of platelets from patients with CKD. Still, a substantial number of studies find platelet function to be unchanged or even enhanced. Further investigation of platelet reactivity in CKD, especially during different CKD stages, is warranted.
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