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      Elevated plasma factor XI predicts cardiovascular events in patients with type 2 diabetes: a long-term observational study

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          Abstract

          Background

          Type 2 diabetes mellitus (T2DM) patients are at high risk of cardiovascular (CV) events. Factor XI (FXI) is associated with arterial thromboembolism, including myocardial infarction (MI), stroke, and CV mortality. The role of FXI in T2DM is unknown. We investigated whether plasma FXI is associated with CV events in T2DM patients in long-term observation.

          Methods

          In 133 T2DM patients (aged 66 ± 8 years, 40.6% women, median T2DM duration 5 [2–10] years) we assessed plasma FXI levels, along with fibrin clot properties, thrombin generation, and fibrinolysis proteins. A composite endpoint of MI, stroke, or CV death, as well as CV mortality alone were assessed during a median follow-up of 72 months.

          Results

          Plasma FXI above the 120% upper normal limit was detected in 25 (18.8%) patients and showed positive association with LDL cholesterol and thrombin activatable fibrinolysis inhibitor, but not glycated hemoglobin, inflammatory markers or thrombin generation. The composite endpoint (n = 21, 15.8%) and CV death alone (n = 16, 12%) were more common in patients with elevated FXI (hazard ratio [HR] 10.94, 95% confidence interval [CI] 4.46–26.87, p < 0.001 and HR 7.11, 95% CI 2.61–19.31, p < 0.001, respectively). On multivariable analysis, FXI remained an independent predictor of the composite endpoint and CV death, regardless of concomitant coronary artery disease.

          Conclusions

          To our knowledge, this study is the first to show that in T2DM patients, elevated FXI could predict major CV events, including mortality, which suggest that anti-FXI agents might be a potential novel antithrombotic option in this disease.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s12933-023-01905-5.

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          Most cited references34

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          Fourth universal definition of myocardial infarction (2018)

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            Thrombin generation and fibrin clot structure.

            Generation of a hemostatic clot requires thrombin-mediated conversion of fibrinogen to fibrin. Previous in vitro studies have demonstrated that the thrombin concentration present at the time of gelation profoundly influences fibrin clot structure. Clots formed in the presence of low thrombin concentrations are composed of thick fibrin fibers and are highly susceptible to fibrinolysis; while, clots formed in the presence of high thrombin concentrations are composed of thin fibers and are relatively resistant to fibrinolysis. While most studies of clot formation have been performed by adding a fixed amount of purified thrombin to fibrinogen, clot formation in vivo occurs in a context of continuous, dynamic changes in thrombin concentration. These changes depend on the local concentrations of pro- and anti-coagulants and cellular activities. Recent studies suggest that patterns of abnormal thrombin generation produce clots with altered fibrin structure and that these changes are associated with an increased risk of bleeding or thrombosis. Furthermore, it is likely that clot structure also contributes to cellular events during wound healing. These findings suggest that studies explicitly evaluating fibrin formation during in situ thrombin generation are warranted to explain and fully appreciate mechanisms of normal and abnormal fibrin clot formation in vivo.
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              The hemostatic system as a modulator of atherosclerosis.

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                Author and article information

                Contributors
                elzbieta.m.paszek@gmail.com
                Journal
                Cardiovasc Diabetol
                Cardiovasc Diabetol
                Cardiovascular Diabetology
                BioMed Central (London )
                1475-2840
                17 July 2023
                17 July 2023
                2023
                : 22
                : 182
                Affiliations
                [1 ]GRID grid.414734.1, ISNI 0000 0004 0645 6500, Clinical Department of Interventional Cardiology, , John Paul II Hospital, ; Krakow, 31-202 Poland
                [2 ]GRID grid.5522.0, ISNI 0000 0001 2162 9631, Department of Thromboembolic Disorders, Institute of Cardiology, , Jagiellonian University Medical College, ; Krakow, 31-202 Poland
                [3 ]GRID grid.5522.0, ISNI 0000 0001 2162 9631, Department of Epidemiology and Population Studies, , Jagiellonian University Medical College, ; Krakow, Poland
                [4 ]GRID grid.5522.0, ISNI 0000 0001 2162 9631, Chair and Department of Endocrinology, , Jagiellonian University Medical College, ; Krakow, Poland
                [5 ]GRID grid.414734.1, ISNI 0000 0004 0645 6500, Department of Diagnostic Medicine, , John Paul II Hospital, ; Krakow, 31-202 Poland
                [6 ]GRID grid.414734.1, ISNI 0000 0004 0645 6500, Krakow Center for Medical Research and Technologies, , John Paul II Hospital, ; Krakow, 31-202 Poland
                Article
                1905
                10.1186/s12933-023-01905-5
                10353137
                37460982
                98bd8857-0ece-4a08-85c0-b8df34c877d0
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 12 May 2023
                : 27 June 2023
                Funding
                Funded by: Jagiellonian University School of Medicine
                Award ID: K/ZDS/000565
                Categories
                Research
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2023

                Endocrinology & Diabetes
                factor xi,type 2 diabetes mellitus,myocardial infarction, stroke, cardiovascular mortality

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