# Type 2 Diabetes Is Associated with Increased Coagulation Activity in Patients with Atrial Fibrillation: A D-Dimer-Based Analysis

**Authors:** Paul Gabriel Ciubotaru, Amit Kohli, Nilima Rajpal Kundnani, Roxana Buzas, Marioara Nicula Neagu, Marius Preda, Vlad-Sabin Ivan, Mihaela-Diana Popa, Milan Daniel Velimirovici, Daniel Florin Lighezan

PMC · DOI: 10.3390/biomedicines14020332 · Biomedicines · 2026-01-31

## TL;DR

This study shows that people with atrial fibrillation and type 2 diabetes have higher blood clotting activity, as measured by D-dimer levels, compared to those without diabetes.

## Contribution

The study demonstrates that T2DM independently increases coagulation activity in AF patients, beyond traditional thromboembolic risk factors.

## Key findings

- T2DM patients had significantly higher D-dimer levels than non-diabetic patients (0.94 vs. 0.63 µg/mL FEU).
- T2DM was independently associated with higher D-dimer levels across all CHA2DS2-VASc categories.
- The association remained significant even among patients on anticoagulation therapy.

## Abstract

Background: Atrial Fibrillation (AF) is associated with a prothrombotic state and increased risk of ischemic stroke. Type 2 diabetes mellitus (T2DM) is a major cardiometabolic comorbidity in AF and independently increases thromboembolic risk. D-dimer is a well-established biomarker of coagulation activation and fibrin turnover, but the specific contribution of T2DM to D-dimer levels in AF remains insufficiently characterized in real-world cohorts. Methods: We conducted a retrospective, observational, single-center study including 300 adult patients with non-valvular AF evaluated at a tertiary university hospital. Patients were stratified according to the presence of T2DM (150 with T2DM and 150 without diabetes). Plasma D-dimer levels were compared between groups and analyzed across clinically relevant thresholds and CHA2DS2-VASc categories. Multivariable linear and logistic regression models were used to assess the independent association between T2DM and D-dimer levels after adjustment for demographic factors, comorbidities, renal function, prior stroke, CHA2DS2-VASc score components, and oral anticoagulation. Results: Patients with T2DM exhibited significantly higher D-dimer levels than non-diabetic patients (median 0.94 vs. 0.63 µg/mL FEU, p < 0.001). T2DM was independently associated with higher log-transformed D-dimer levels (adjusted β = 0.19, p < 0.001) and with increased odds of elevated D-dimer above both 0.5 µg/mL and 1.0 µg/mL thresholds. Across all CHA2DS2-VASc categories, patients with T2DM consistently showed higher D-dimer concentrations. Findings remained robust in sensitivity analyses restricted to anticoagulated patients. Conclusions: In patients with atrial fibrillation, type 2 diabetes mellitus is associated with increased coagulation activity as reflected by higher D-dimer levels, independent of clinical thromboembolic risk. These results support the concept of a diabetes-associated hypercoagulable AF phenotype and highlight the potential role of coagulation biomarkers in refining risk stratification.

## Linked entities

- **Diseases:** Atrial Fibrillation (MONDO:0004981), Type 2 diabetes mellitus (MONDO:0005148), ischemic stroke (MONDO:1060198)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, PLG (plasminogen) [NCBI Gene 5340] {aka HAE4}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SERPINE1 (serpin family E member 1) [NCBI Gene 5054] {aka PAI, PAI-1, PAI1, PLANH1}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, PLAT (plasminogen activator, tissue type) [NCBI Gene 5327] {aka T-PA, TPA}, F7 (coagulation factor VII) [NCBI Gene 2155] {aka SPCA}, VWF (von Willebrand factor) [NCBI Gene 7450] {aka F8VWF, VWD}
- **Diseases:** vascular (MESH:D057772), arterial and venous thrombotic (MESH:D020246), insulin resistance (MESH:D007333), CKD (MESH:D051436), infection (MESH:D007239), cardiovascular conditions (MESH:D002318), coagulation (MESH:D001778), myocardial infarction (MESH:D009203), malignancy (MESH:D009369), ischemic stroke (MESH:D002544), Diabetes (MESH:D003920), end-stage kidney disease (MESH:D007676), Endothelial dysfunction (MESH:D014652), COVID-19 infection (MESH:D000086382), AF (MESH:D001281), ischemic (MESH:D002545), death (MESH:D003643), venous thromboembolism (MESH:D054556), hyperglycemic (MESH:D006944), Hypertension (MESH:D006973), arterial hypertension (MESH:D000081029), major bleeding (MESH:D004830), intracranial bleeding (MESH:D013345), inflammation (MESH:D007249), injury to (MESH:D014947), transient (MESH:C563551), hyperglycemia (MESH:D006943), endothelial abnormalities (MESH:D000014), atrial thrombus (MESH:D013927), cardiometabolic (MESH:D024821), endothelial (MESH:D005642), disseminated intravascular coagulation (MESH:D004211), metabolic (MESH:D008659), oncologic (MESH:D000072716), electrical disorder (MESH:D004556), acute and (MESH:D000208), arrhythmic disease (OMIM:212500), diabetic vasculopathy (MESH:D003925), abnormal renal or liver function (MESH:D056486), Thromboembolic (MESH:D013923), rheumatic mitral stenosis (MESH:D008946), chronic obstructive pulmonary disease (MESH:D029424), atrial cardiomyopathy (MESH:D009202), blood stasis (MESH:D014647), Chronic low (MESH:D009800), coronary artery disease (MESH:D003324), hypercoagulability (MESH:D019851), stroke (MESH:D020521), TIA (MESH:D002546), cardiac structural or functional abnormality (MESH:C566527), peripheral arterial disease (MESH:D058729), T2DM (MESH:D003924), embolic (MESH:D004617), bleeding (MESH:D006470), arrhythmia (MESH:D001145), Heart failure (MESH:D006333)
- **Chemicals:** natriuretic peptides (MESH:D045265), vitamin K (MESH:D014812), D (MESH:D003903), DOAC (-), nitric oxide (MESH:D009569), glucose (MESH:D005947), insulin (MESH:D007328), warfarin (MESH:D014859), alcohol (MESH:D000438), metformin (MESH:D008687)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

84 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938132/full.md

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Source: https://tomesphere.com/paper/PMC12938132