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Rosuvastatin use reduces thrombin generation potential in patients with venous thromboembolism: a randomized controlled trial
ESSENTIALS: The role of statins in hemostasis and venous thromboembolism (VTE) prophylaxis is not clear. This trial assessed whether rosuvastatin use affects thrombin generation in patients with VTE. Endogenous thrombin potential and peak were decreased by 10% and 5% with rosuvastatin therapy. These...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850636/ https://www.ncbi.nlm.nih.gov/pubmed/30565854 http://dx.doi.org/10.1111/jth.14364 |
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author | Orsi, Fernanda A. Biedermann, Joseph S. Kruip, Marieke J.H.A. van der Meer, Felix J. Rosendaal, Frits R. van Hylckama Vlieg, Astrid Bos, Mettine H. A. Leebeek, Frank W. G. Cannegieter, Suzanne C. Lijfering, Willem M. |
author_facet | Orsi, Fernanda A. Biedermann, Joseph S. Kruip, Marieke J.H.A. van der Meer, Felix J. Rosendaal, Frits R. van Hylckama Vlieg, Astrid Bos, Mettine H. A. Leebeek, Frank W. G. Cannegieter, Suzanne C. Lijfering, Willem M. |
author_sort | Orsi, Fernanda A. |
collection | PubMed |
description | ESSENTIALS: The role of statins in hemostasis and venous thromboembolism (VTE) prophylaxis is not clear. This trial assessed whether rosuvastatin use affects thrombin generation in patients with VTE. Endogenous thrombin potential and peak were decreased by 10% and 5% with rosuvastatin therapy. These results provide basis for trials on the efficacy of statins in reducing recurrent VTE risk. SUMMARY: BACKGROUND: Statin therapy could form an alternative prophylactic treatment for venous thromboembolism (VTE) if statins are proven to downregulate hemostasis and prevent recurrent VTE, without increasing bleeding risk. OBJECTIVES: The STAtins Reduce Thrombophilia (START) trial investigated whether statin affects coagulation in patients with prior VTE. PATIENTS/METHODS: After anticoagulation withdrawal, patients were randomized to rosuvastatin 20 mg day(−1) for 4 weeks or no intervention. Plasma samples taken at baseline and at the end of the study were analyzed employing thrombin generation assay. RESULTS AND CONCLUSIONS: The study comprised 126 rosuvastatin users and 119 non‐users. Mean age was 58 years, 61% were men, 49% had unprovoked VTE and 75% had cardiovascular (CV) risk factors. Endogenous thrombin potential (ETP) increased from baseline to end of study in non‐statin users (mean 97.22 nm*min; 95% CI, 40.92–153.53) and decreased in rosuvastatin users (mean −24.94 nm*min; 95% CI, −71.81 to 21.93). The mean difference in ETP change between treatments was −120.24 nm*min (95% CI, −192.97 to −47.51), yielding a 10.4% ETP reduction by rosuvastatin. The thrombin peak increased in both non‐statin (mean 20.69 nm; 95% CI, 9.80–31.58) and rosuvastatin users (mean 8.41 nm; 95% CI −0.86 to 17.69). The mean difference in peak change between treatments was −11.88 nm (95% CI, −26.11 to 2.35), yielding a 5% peak reduction by rosuvastatin. Other thrombin generation parameters did not change substantially. The reduction in ETP and peak by rosuvastatin was more pronounced in the subgroups of participants with CV risk factors and with unprovoked VTE. We conclude that rosuvastatin reduces thrombin generation potential in patients who had VTE. |
format | Online Article Text |
id | pubmed-6850636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68506362019-11-18 Rosuvastatin use reduces thrombin generation potential in patients with venous thromboembolism: a randomized controlled trial Orsi, Fernanda A. Biedermann, Joseph S. Kruip, Marieke J.H.A. van der Meer, Felix J. Rosendaal, Frits R. van Hylckama Vlieg, Astrid Bos, Mettine H. A. Leebeek, Frank W. G. Cannegieter, Suzanne C. Lijfering, Willem M. J Thromb Haemost CLINICAL HEMOSTASIS AND THROMBOSIS ESSENTIALS: The role of statins in hemostasis and venous thromboembolism (VTE) prophylaxis is not clear. This trial assessed whether rosuvastatin use affects thrombin generation in patients with VTE. Endogenous thrombin potential and peak were decreased by 10% and 5% with rosuvastatin therapy. These results provide basis for trials on the efficacy of statins in reducing recurrent VTE risk. SUMMARY: BACKGROUND: Statin therapy could form an alternative prophylactic treatment for venous thromboembolism (VTE) if statins are proven to downregulate hemostasis and prevent recurrent VTE, without increasing bleeding risk. OBJECTIVES: The STAtins Reduce Thrombophilia (START) trial investigated whether statin affects coagulation in patients with prior VTE. PATIENTS/METHODS: After anticoagulation withdrawal, patients were randomized to rosuvastatin 20 mg day(−1) for 4 weeks or no intervention. Plasma samples taken at baseline and at the end of the study were analyzed employing thrombin generation assay. RESULTS AND CONCLUSIONS: The study comprised 126 rosuvastatin users and 119 non‐users. Mean age was 58 years, 61% were men, 49% had unprovoked VTE and 75% had cardiovascular (CV) risk factors. Endogenous thrombin potential (ETP) increased from baseline to end of study in non‐statin users (mean 97.22 nm*min; 95% CI, 40.92–153.53) and decreased in rosuvastatin users (mean −24.94 nm*min; 95% CI, −71.81 to 21.93). The mean difference in ETP change between treatments was −120.24 nm*min (95% CI, −192.97 to −47.51), yielding a 10.4% ETP reduction by rosuvastatin. The thrombin peak increased in both non‐statin (mean 20.69 nm; 95% CI, 9.80–31.58) and rosuvastatin users (mean 8.41 nm; 95% CI −0.86 to 17.69). The mean difference in peak change between treatments was −11.88 nm (95% CI, −26.11 to 2.35), yielding a 5% peak reduction by rosuvastatin. Other thrombin generation parameters did not change substantially. The reduction in ETP and peak by rosuvastatin was more pronounced in the subgroups of participants with CV risk factors and with unprovoked VTE. We conclude that rosuvastatin reduces thrombin generation potential in patients who had VTE. John Wiley and Sons Inc. 2019-02-03 2019-02 /pmc/articles/PMC6850636/ /pubmed/30565854 http://dx.doi.org/10.1111/jth.14364 Text en © 2018 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals, Inc. on behalf of International Society on Thrombosis and Haemostasis. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | CLINICAL HEMOSTASIS AND THROMBOSIS Orsi, Fernanda A. Biedermann, Joseph S. Kruip, Marieke J.H.A. van der Meer, Felix J. Rosendaal, Frits R. van Hylckama Vlieg, Astrid Bos, Mettine H. A. Leebeek, Frank W. G. Cannegieter, Suzanne C. Lijfering, Willem M. Rosuvastatin use reduces thrombin generation potential in patients with venous thromboembolism: a randomized controlled trial |
title | Rosuvastatin use reduces thrombin generation potential in patients with venous thromboembolism: a randomized controlled trial |
title_full | Rosuvastatin use reduces thrombin generation potential in patients with venous thromboembolism: a randomized controlled trial |
title_fullStr | Rosuvastatin use reduces thrombin generation potential in patients with venous thromboembolism: a randomized controlled trial |
title_full_unstemmed | Rosuvastatin use reduces thrombin generation potential in patients with venous thromboembolism: a randomized controlled trial |
title_short | Rosuvastatin use reduces thrombin generation potential in patients with venous thromboembolism: a randomized controlled trial |
title_sort | rosuvastatin use reduces thrombin generation potential in patients with venous thromboembolism: a randomized controlled trial |
topic | CLINICAL HEMOSTASIS AND THROMBOSIS |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850636/ https://www.ncbi.nlm.nih.gov/pubmed/30565854 http://dx.doi.org/10.1111/jth.14364 |
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