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Updated: Oct 5, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Evaluation of novel coagulation and platelet function assays in patients with chronic kidney disease
Alyaa Abdelmaguid1,2,3, Lara N Roberts4, Laura Tugores5
1Department of Women and Children's Health, King's College London, London, UK.
Insights
Chronic kidney disease (CKD) patients show increased clotting (hypercoagulability) and impaired platelet function. Estimated glomerular filtration rate (eGFR) independently influences these hemostasis abnormalities in CKD.
Area of Science:
- Nephrology
- Hematology
- Clinical Chemistry
Background:
- Hemostasis evaluation is crucial for managing bleeding and thrombotic risks in chronic kidney disease (CKD).
- Standard coagulation tests are insufficient for detecting coagulopathy in CKD patients.
- Novel assays are needed to accurately assess hemostasis in CKD.
Purpose of the Study:
- To investigate hemostasis parameters in patients across various stages of chronic kidney disease (CKD).
- To utilize advanced coagulation assays for a comprehensive hemostasis evaluation in CKD.
- To correlate hemostasis findings with estimated glomerular filtration rate (eGFR) in CKD.
Main Methods:
- Cross-sectional study involving 120 CKD patients and 30 healthy controls (HC).
- Utilized standard coagulation tests alongside rotational thromboelastometry (ROTEM), multiple electrode aggregometry (MEA), and thrombin generation assays.
- Measured biomarkers including D-dimer, thrombin-antithrombin (TAT), and intercellular adhesion molecule-1 (ICAM-1).
Main Results:
- CKD patients exhibited elevated D-dimer, TAT, and ICAM-1 levels compared to HC (P < .01).
- ROTEM showed significantly higher maximum clot firmness in CKD patients (P < .01).
- Stage 5 CKD patients displayed impaired platelet aggregation (MEA) and prolonged thrombin generation times.
Conclusions:
- CKD patients present with concurrent hypercoagulability (ROTEM) and platelet dysfunction (MEA).
- Estimated glomerular filtration rate (eGFR) is an independent determinant of both hypercoagulability and platelet dysfunction in CKD.
- Advanced coagulation assays provide critical insights into CKD-associated hemostatic abnormalities.
Background:
Hemostasis evaluation in chronic kidney disease (CKD) is critical for optimal management of thrombotic and bleeding events. Standard coagulation screens are inadequate for predicting coagulopathy in CKD.
Objective:
To evaluate hemostasis parameters in patients with different stages of CKD using novel coagulation assays.
Patients/Methods:
Cross-sectional study of 30 healthy controls (HC) and 120 CKD patients (10 Stage 2, 20 Stage 3, 20 Stage 4, 20 Stage 5 not requiring renal replacement therapy, 20 transplant, 10 newly started on hemodialysis [HD], 20 established on HD). Standard laboratory tests were performed in addition to rotational thromboelastometry (ROTEM), multiple electrode aggregometry (MEA), thrombin generation assays, D-dimer, and markers of thrombogenesis (thrombin-antithrombin [TAT]), fibrinolysis, and endothelial activation (intercellular adhesion molecule-1 [ICAM-1]).
Results:
D-dimer, TAT, and ICAM-1 concentrations were significantly higher in patients with CKD than HC (P < .01). ROTEM maximum clot firmness was significantly higher in patients than in HC (P < .01). In CKD Stage 5 patients (pre-HD and started HD) adenosine diphosphate and thrombin receptor activating peptide MEA tests were significantly lower than HC indicating platelet aggregation defect (P < .05). Multivariate analysis confirmed the direct effect of estimated glomerular filtration rate (eGFR) in the variance of ROTEM and MEA tests. Endogenous thrombin potential and peak thrombin were not statistically different between groups, but Stage 5 CKD patients had prolonged lag time (7.91 vs. 6.33, P < .001) and time to thrombin peak (10.8 vs. 9.5, P < .05) compared to HC.
Conclusions:
Patients with CKD exhibit features of concomitant hypercoagulability measured by ROTEM and platelet dysfunction measured with MEA. eGFR was an independent determinant of platelet dysfunction and hypercoagulability.
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