Homoarginine and methylarginines independently predict long-term outcome in patients presenting with suspicion of venous thromboembolism.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
05 05 2021
Historique:
received: 08 01 2021
accepted: 12 04 2021
entrez: 6 5 2021
pubmed: 7 5 2021
medline: 25 2 2023
Statut: epublish

Résumé

Endogenous arginine derivatives homoarginine, asymmetric dimethylarginine (ADMA) and symmetric dimethyarginine (SDMA) are independent mortality predictors in atherosclerotic cardiovascular disease (CVD). Our study reports the first analysis, whether homoarginine, ADMA and SDMA predict venous thromboembolism (VTE) recurrence and overall mortality in patients with suspected acute VTE. We assessed serum levels of homoarginine, ADMA and SDMA by LC-MS/MS in 865 individuals from a prospective consecutive cohort of patients with clinical suspicion of VTE. The median follow-up time for mortality was 1196 days. VTE was confirmed by imaging in 418 patients and excluded in 447 patients. Low levels of homoarginine and high levels of ADMA or SDMA independently predicted all-cause mortality after adjustment for sex, age, oral anticoagulants, body mass index, arterial hypertension, diabetes mellitus, smoking, dyslipidemia, chronic heart failure, history of stroke, creatinine and cancer both in patients with VTE and without VTE. Interestingly, none of those parameters was predictive for VTE recurrence. We provide the first report that low circulating levels of homoarginine and high circulating levels of ADMA and SDMA independently predict all-cause mortality in patients with suspected VTE. These parameters might serve as markers of "frailty" and should be considered for future risk stratification approaches in this clinical population. Taking into account that homoarginine supplementation is protective in animal models of CVD and safe in healthy human volunteers, our study provides the basis for future homoarginine supplementation studies in patients with suspected VTE to investigate possible direct protective effects of homoarginine in this population.

Identifiants

pubmed: 33953241
doi: 10.1038/s41598-021-88986-y
pii: 10.1038/s41598-021-88986-y
pmc: PMC8100302
doi:

Substances chimiques

Homoarginine 156-86-5
Arginine 94ZLA3W45F

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

9569

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Auteurs

Roman N Rodionov (RN)

Division of Angiology, Department of Internal Medicine III, University Center for Vascular Medicine, University Hospital Carl Gustav Carus, Technische Universität Dresden, Fetscherstraße 74, 01307, Dresden, Germany. Roman.Rodionov@uniklinikum-dresden.de.
College of Medicine and Public Health, Flinders University and Flinders Medical Centre, Adelaide, Australia. Roman.Rodionov@uniklinikum-dresden.de.

Jan Beyer-Westendorf (J)

Division of Hematology, Hemostaseology and Coagulation, Department of Medicine I, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Kings Thrombosis Service, Department of Hematology, Kings College London, London, UK.

Stefanie M Bode-Böger (SM)

Institute of Clinical Pharmacology, Otto-von-Guericke University, Magdeburg, Germany.

Lisa Eggebrecht (L)

Department of Preventive Cardiology and Preventive Medicine, Center for Cardiology, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.

Stavros Konstantinides (S)

Clinical Epidemiology and Systems Medicine, Center for Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.
Department of Cardiology, Democritus University of Thrace, University General Hospital, Alexandroupoli, Greece.

Jens Martens-Lobenhoffer (J)

Institute of Clinical Pharmacology, Otto-von-Guericke University, Magdeburg, Germany.

Markus Nagler (M)

Department of Preventive Cardiology and Preventive Medicine, Center for Cardiology, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.
Clinical Epidemiology and Systems Medicine, Center for Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.

Jürgen Prochaska (J)

Department of Preventive Cardiology and Preventive Medicine, Center for Cardiology, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.
Clinical Epidemiology and Systems Medicine, Center for Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Rhine-Main, Mainz, Germany.

Philipp Wild (P)

Department of Preventive Cardiology and Preventive Medicine, Center for Cardiology, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany. Philipp.Wild@unimedizin-mainz.de.
Clinical Epidemiology and Systems Medicine, Center for Thrombosis and Hemostasis, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany. Philipp.Wild@unimedizin-mainz.de.
German Center for Cardiovascular Research (DZHK), Partner Site Rhine-Main, Mainz, Germany. Philipp.Wild@unimedizin-mainz.de.

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