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DOI: 10.1055/a-2747-8963
Occurrence of Platelet–Monocyte Aggregates in Patients with Metabolic Disorders and Effect of Direct Anticoagulants
Authors
Funding Information This work was supported by the Czech Health Research Council (grant no. NU21J-02–00021); Charles University (PRIMUS/25/MED/001 and SVV 260 549) and MH CZ - DRO (grant no. UHHK, 00179906).

Abstract
Background
Platelet–monocyte aggregates (PMA) are modern biomarkers for the early onset of cardiovascular diseases (CVD). PMA occur in the presence of activated platelets (AP), whose incidence is higher in patients with metabolic diseases. These patients frequently benefit from anticoagulant therapy, particularly in advanced disease stages. However, the impact of these drugs on PMA occurrence is unknown.
Materials and Methods
Blood samples from healthy volunteers, patients with type 1 diabetes mellitus (DMT1), type 2 diabetes mellitus (DMT2), dyslipidemia (hypercholesterolemia), and severe forms of familial hypercholesterolemia (FH) were analyzed by flow cytometry to detect both AP and PMA. Subsequently, blood samples were treated with four direct anticoagulants (rivaroxaban, apixaban, dabigatran, or argatroban, all at a final concentration of 1 µM), and PMA were again detected. Anthropological and biochemical parameters were recorded and correlated with AP and PMA.
Results
AP levels were higher solely in DMT2 patients, but PMA occurrence was significantly increased in all patient groups in comparison to that of generally healthy donors, except for FH patients. No sex-related differences were observed, but an increasing trend in AP and PMA incidence was observed with increasing age and BMI. Significant correlations of AP and PMA with anthropological and biochemical parameters were found solely in some groups of patients or in some anticoagulant-treated samples. Only argatroban and apixaban-treated samples significantly decreased PMA occurrence, and this was observed solely in the dyslipidemia patient group.
Conclusion
These findings suggest a potential positive outcome of anticoagulant treatment for metabolic disease patients and confirm PMA as a sensitive marker in patients with metabolic diseases.
Data Availability Statement
The data that support the findings of this study are available from the corresponding author upon reasonable request. Some data may not be made available because of privacy or ethical restrictions.
Contributors' Statement
C.G. contributed to investigation, formal analysis, writing—original draft; Z.L. contributed to investigation, writing—review and editing; M.H. contributed to investigation, writing—review and editing; M.P. contributed to investigation, writing—review and editing; P.S. contributed to investigation, writing—review and editing, funding acquisition; K.M. contributed to investigation, writing—review and editing; D.T. contributed to investigation, writing—review and editing; L.K.K. contributed to investigation, writing—review and editing, funding acquisition, supervision; M.B. contributed to methodology, supervision, writing—review and editing; V.B. contributed to methodology, supervision, writing—review and editing; P.M. contributed to conceptualization, methodology, formal analysis, writing—original draft, writing—review and editing, funding acquisition, supervision; A.C. contributed to conceptualization, methodology, investigation, formal analysis, writing—review and editing, funding acquisition, supervision. All authors read and approved the submitted version of the manuscript.
Ethical Approval
This study was approved by the Ethics Committee of the University Hospital in Hradec Králové (No. 202007 S01P from June 18, 2020). All experiments conformed to the latest Declaration of Helsinki.
Publication History
Received: 07 May 2025
Accepted after revision: 13 November 2025
Article published online:
05 December 2025
© 2025. Thieme. All rights reserved.
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