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Serum amyloid A4 is a procoagulant apolipoprotein that it is elevated in venous thrombosis patients

BACKGROUND: Serum amyloid A4 (SAA4) is an apolipoprotein that is in the SAA family and it is constitutively translated. Previously, acute‐phase SAA1 and SAA2 levels were associated with venous thromboembolism (VTE). OBJECTIVE: We investigated the association of plasma SAA4 with VTE and the role of S...

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Autores principales: Fernández, José A., Deguchi, Hiroshi, Elias, Darlene J., Griffin, John H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7040552/
https://www.ncbi.nlm.nih.gov/pubmed/32110751
http://dx.doi.org/10.1002/rth2.12291
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author Fernández, José A.
Deguchi, Hiroshi
Elias, Darlene J.
Griffin, John H.
author_facet Fernández, José A.
Deguchi, Hiroshi
Elias, Darlene J.
Griffin, John H.
author_sort Fernández, José A.
collection PubMed
description BACKGROUND: Serum amyloid A4 (SAA4) is an apolipoprotein that is in the SAA family and it is constitutively translated. Previously, acute‐phase SAA1 and SAA2 levels were associated with venous thromboembolism (VTE). OBJECTIVE: We investigated the association of plasma SAA4 with VTE and the role of SAA4 in coagulation. PATIENTS AND METHODS: The association of SAA4 with VTE in a case‐control study of adult VTE subjects (N = 113 each group) and the effects of recombinant SAA4 on plasma blood coagulation assays and prothrombin activation initiated by factor Xa were evaluated. RESULTS: Plasma SAA4 levels in VTE subjects were higher vs. controls (48.1 vs. 38.4 µg/mL; P < .001). Elevated plasma SAA4 level (above the 90th percentile of controls) was associated with increased VTE occurrence (odds ratio, 3.8; 95% confidence interval, 1.8‐8.0). This association remained significant after the adjustment for acute‐phase SAA level, suggesting that SAA4 associated with VTE is independent of acute‐phase SAA. Two isoforms of SAA4, that is, glycosylated and nonglycosylated SAA4 isoforms, were each higher in VTE patients. When recombinant SAA4 was added to plasma, it shortened factor Xa‐1‐stage clotting times, showing that it enhances clotting in plasma. In reaction mixtures containing purified factors Xa and Va and prothrombin, recombinant SAA4 increased prothrombin activation, showing that it enhances prothrombinase activity. CONCLUSION: Elevated plasma constitutive SAA4 levels were linked to VTE in adults, and SAA4 can enhance thrombin generation in plasma. Our data highlight a previously unknown procoagulant activity of SAA4 that appears to be related to risk of venous thrombotic events.
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spelling pubmed-70405522020-02-27 Serum amyloid A4 is a procoagulant apolipoprotein that it is elevated in venous thrombosis patients Fernández, José A. Deguchi, Hiroshi Elias, Darlene J. Griffin, John H. Res Pract Thromb Haemost Original Articles: Thrombosis BACKGROUND: Serum amyloid A4 (SAA4) is an apolipoprotein that is in the SAA family and it is constitutively translated. Previously, acute‐phase SAA1 and SAA2 levels were associated with venous thromboembolism (VTE). OBJECTIVE: We investigated the association of plasma SAA4 with VTE and the role of SAA4 in coagulation. PATIENTS AND METHODS: The association of SAA4 with VTE in a case‐control study of adult VTE subjects (N = 113 each group) and the effects of recombinant SAA4 on plasma blood coagulation assays and prothrombin activation initiated by factor Xa were evaluated. RESULTS: Plasma SAA4 levels in VTE subjects were higher vs. controls (48.1 vs. 38.4 µg/mL; P < .001). Elevated plasma SAA4 level (above the 90th percentile of controls) was associated with increased VTE occurrence (odds ratio, 3.8; 95% confidence interval, 1.8‐8.0). This association remained significant after the adjustment for acute‐phase SAA level, suggesting that SAA4 associated with VTE is independent of acute‐phase SAA. Two isoforms of SAA4, that is, glycosylated and nonglycosylated SAA4 isoforms, were each higher in VTE patients. When recombinant SAA4 was added to plasma, it shortened factor Xa‐1‐stage clotting times, showing that it enhances clotting in plasma. In reaction mixtures containing purified factors Xa and Va and prothrombin, recombinant SAA4 increased prothrombin activation, showing that it enhances prothrombinase activity. CONCLUSION: Elevated plasma constitutive SAA4 levels were linked to VTE in adults, and SAA4 can enhance thrombin generation in plasma. Our data highlight a previously unknown procoagulant activity of SAA4 that appears to be related to risk of venous thrombotic events. John Wiley and Sons Inc. 2019-12-29 /pmc/articles/PMC7040552/ /pubmed/32110751 http://dx.doi.org/10.1002/rth2.12291 Text en © 2019 The Authors. Research and Practice in 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 Original Articles: Thrombosis
Fernández, José A.
Deguchi, Hiroshi
Elias, Darlene J.
Griffin, John H.
Serum amyloid A4 is a procoagulant apolipoprotein that it is elevated in venous thrombosis patients
title Serum amyloid A4 is a procoagulant apolipoprotein that it is elevated in venous thrombosis patients
title_full Serum amyloid A4 is a procoagulant apolipoprotein that it is elevated in venous thrombosis patients
title_fullStr Serum amyloid A4 is a procoagulant apolipoprotein that it is elevated in venous thrombosis patients
title_full_unstemmed Serum amyloid A4 is a procoagulant apolipoprotein that it is elevated in venous thrombosis patients
title_short Serum amyloid A4 is a procoagulant apolipoprotein that it is elevated in venous thrombosis patients
title_sort serum amyloid a4 is a procoagulant apolipoprotein that it is elevated in venous thrombosis patients
topic Original Articles: Thrombosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7040552/
https://www.ncbi.nlm.nih.gov/pubmed/32110751
http://dx.doi.org/10.1002/rth2.12291
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