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ArticleFrontiers in cardiovascular medicine2026

The impact of body composition variability on coagulation monitoring in patients on direct oral factor Xa inhibitors for treatment of venous thromboembolism.

Katharina Kurzmann-Guetl, Deborah R Leitner, Thomas Gary, Alexander Avian, Andrea Beck, Jasmin Rabensteiner, Florian Prueller, Reinhard B Raggam, Marianne Brodmann, Hermann Toplak

Abstract read
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Article in Frontiers in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Katharina Kurzmann-Guetl *Division of Angiology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Deborah R Leitner *Lipid Clinic, Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Thomas GaryDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Alexander AvianMedical Institute for Medical Informatics, Statistics and Documentation, Medical University of Graz, Graz, Austria.
Andrea BeckLipid Clinic, Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Jasmin RabensteinerClinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University Graz, Graz, Austria.
Florian PruellerClinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University Graz, Graz, Austria.
Reinhard B RaggamDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Marianne BrodmannDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Hermann ToplakLipid Clinic, Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/objectives: Evidence for the first-line treatment of venous thromboembolism (VTE) by use of direct oral anticoagulants (DOACs) is based on stratification by body-mass index (BMI) and total body weight, but does not consider body composition - defined as the distribution of fat mass (FM) and fat-free mass (FFM). Variability in body composition exists among patients with normal BMI, but is anticipated to be markedly greater in the context of overweight and obesity. Methods: The BIARIVA prospective, single-center, cross-sectional study was conducted to assess whether body composition affects blood coagulation monitoring parameters in patients on therapeutic-dose anticoagulant treatment for VTE with oral factor (F.) Xa inhibitors rivaroxaban or edoxaban. Patients were qualified for inclusion into the study if they were categorized into one of the specified BMI categories; 18-25, 30-35, or > 35 kg/m Results: Thirty-six patients on rivaroxaban and 35 patients on edoxaban were finally analyzed. The main finding in this study was a significant negative correlation observed in the edoxaban group for the absolute FFM with anti-F.Xa and plasma concentration peak levels (BIA method 1: r Conclusions: This study suggests that body composition might influence specific coagulation measurements in patients treated with edoxaban, but further research is required to finally determine the role of body composition in this context and to evaluate clinical implications.

Indexed as

anticoagulationbody compositionobesityoral factor Xa inhibitorsvenous thromboembolism

Identifiers

PMID41908060
PMCPMC13021583

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