Objectives Growth differentiation factor-15 (GDF-15) has emerged as a novel biomarker for coronary artery disease (CAD). Although a hypercoagulable state is recognized as a biological mechanism triggering cardiac events in CAD, the relationship between GDF-15 and coagulation parameters in CAD patients remains unclear.
Methods We screened male patients who underwent elective coronary angiography for suspected CAD at Renmin Hospital of Wuhan University between January 2020 and December 2020, and enrolled those with confirmed diagnoses. Serum GDF-15 levels, blood cell counts, glucose, serum lipids, and coagulation parameters were measured.
Results A total of 892 subjects were included (592 CAD patients and 300 controls). The CAD group comprised 161 stable angina (SA) and 431 acute coronary syndrome (ACS) cases. Data were analyzed using Kruskal–Wallis one-way ANOVA with post hoc tests (Holm–Sidak and Dunn’s tests). Compared with controls, CAD patients showed significantly higher serum GDF-15 levels. When stratified by GDF-15 tertiles, patients with high GDF-15 levels exhibited prolonged prothrombin time (PT) and activated partial thromboplastin time (APTT), elevated fibrinogen and D-dimer levels, and reduced antithrombin III (AT3) activity (all P<0.01). Multiple linear regression revealed that GDF-15 was independently associated with fibrinogen in all CAD patients (β=0.208, P<0.001) as well as in SA (β=0.171, P=0.035) and ACS subgroups (β=0.163, P=0.006). Additionally, GDF-15 negatively correlated with AT3 in the ACS subgroup (β= −0.120, P=0.039).
Conclusions Elevated GDF-15 levels in male CAD patients are associated with altered coagulation parameters, suggesting that GDF-15 may serve as a potential indicator of thrombosis risk in cardiovascular management.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study was funded by Fundamental Research Funds for Central Universities (Grant Number:2042021kf0109)
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
Ethics committee of Renmin Hospital of Wuhan University gave ethical approval for this work
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I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
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Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors.
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