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Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura

In the pathogenesis of thrombotic thrombocytopenic purpura (TTP), reductions in the enzyme activity of ADAMTS13, which cuts ultralarge von Willebrand multimers, generates shear stress on the microvascular endothelium, leading to platelet aggregation and the formation of a thrombus. ADAMTS13 activity...

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Autores principales: Nakamura, Kensuke, Inokuchi, Ryota, Hiruma, Takahiro, Ohshima, Kazuma, Sonoo, Tomohiro, Tokunaga, Kurato, Doi, Kent, Nakajima, Susumu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998437/
https://www.ncbi.nlm.nih.gov/pubmed/27310951
http://dx.doi.org/10.1097/MD.0000000000003712
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author Nakamura, Kensuke
Inokuchi, Ryota
Hiruma, Takahiro
Ohshima, Kazuma
Sonoo, Tomohiro
Tokunaga, Kurato
Doi, Kent
Nakajima, Susumu
author_facet Nakamura, Kensuke
Inokuchi, Ryota
Hiruma, Takahiro
Ohshima, Kazuma
Sonoo, Tomohiro
Tokunaga, Kurato
Doi, Kent
Nakajima, Susumu
author_sort Nakamura, Kensuke
collection PubMed
description In the pathogenesis of thrombotic thrombocytopenic purpura (TTP), reductions in the enzyme activity of ADAMTS13, which cuts ultralarge von Willebrand multimers, generates shear stress on the microvascular endothelium, leading to platelet aggregation and the formation of a thrombus. ADAMTS13 activity is markedly decreased in typical TTP, but is only mildly reduced in secondary TTP, which concomitantly develops with primary disease. The latter develops with septic disseminated intravascular coagulation (DIC) and often causes organ failure. Recombinant thrombomodulin (rTM) is a drug that is used to treat DIC and may also remit TTP because it improves vascular endothelial dysfunction. Therefore, we herein investigated the efficacy of rTM in patients treated for the pathology of secondary TTP. Patients who were admitted to the Emergency and Critical Care Center of our hospital and met the following conditions were extracted and retrospectively analyzed: hemolytic anemia accompanied by fragmented red blood cells (Hb < 12 g/dL or lower); thrombocytopenia (<100 × 10(3)/μL); and ADAMTS13 activity <50%. Sixteen patients were included and accompanied by Kidney Disease: Improving Global Outcomes (KDIGO) stage 2 or more severe nephropathy and DIC. Eleven and 5 patients treated with and without rTM (the rTM and non-rTM treatment groups, respectively) were compared, and no significant difference was noted in their basic characteristics, such as background disease and severity. No significant difference was observed in survival rates; however, the platelet count, which is an important outcome of treatments for TTP, significantly increased in the rTM treatment group: 3.3 ± 2.6→11.3 ± 14.6 versus 3.5 ± 3.7→5.7 ± 3.9 (×1000/μL) (P = 0.034). Thrombotic thrombocytopenic purpura originally requires invasive treatments and its prognosis is not favorable. Blood thrombomodulin levels also markedly increase due to vascular endothelial dysfunction, whereas rTM alleviates vascular endothelial dysfunction in TTP patients with high blood TM levels, suggesting the importance of administering rTM. Thus, rTM may be effective for secondary TTP and may be adopted as adjuvant therapy.
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spelling pubmed-49984372016-09-02 Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura Nakamura, Kensuke Inokuchi, Ryota Hiruma, Takahiro Ohshima, Kazuma Sonoo, Tomohiro Tokunaga, Kurato Doi, Kent Nakajima, Susumu Medicine (Baltimore) 3900 In the pathogenesis of thrombotic thrombocytopenic purpura (TTP), reductions in the enzyme activity of ADAMTS13, which cuts ultralarge von Willebrand multimers, generates shear stress on the microvascular endothelium, leading to platelet aggregation and the formation of a thrombus. ADAMTS13 activity is markedly decreased in typical TTP, but is only mildly reduced in secondary TTP, which concomitantly develops with primary disease. The latter develops with septic disseminated intravascular coagulation (DIC) and often causes organ failure. Recombinant thrombomodulin (rTM) is a drug that is used to treat DIC and may also remit TTP because it improves vascular endothelial dysfunction. Therefore, we herein investigated the efficacy of rTM in patients treated for the pathology of secondary TTP. Patients who were admitted to the Emergency and Critical Care Center of our hospital and met the following conditions were extracted and retrospectively analyzed: hemolytic anemia accompanied by fragmented red blood cells (Hb < 12 g/dL or lower); thrombocytopenia (<100 × 10(3)/μL); and ADAMTS13 activity <50%. Sixteen patients were included and accompanied by Kidney Disease: Improving Global Outcomes (KDIGO) stage 2 or more severe nephropathy and DIC. Eleven and 5 patients treated with and without rTM (the rTM and non-rTM treatment groups, respectively) were compared, and no significant difference was noted in their basic characteristics, such as background disease and severity. No significant difference was observed in survival rates; however, the platelet count, which is an important outcome of treatments for TTP, significantly increased in the rTM treatment group: 3.3 ± 2.6→11.3 ± 14.6 versus 3.5 ± 3.7→5.7 ± 3.9 (×1000/μL) (P = 0.034). Thrombotic thrombocytopenic purpura originally requires invasive treatments and its prognosis is not favorable. Blood thrombomodulin levels also markedly increase due to vascular endothelial dysfunction, whereas rTM alleviates vascular endothelial dysfunction in TTP patients with high blood TM levels, suggesting the importance of administering rTM. Thus, rTM may be effective for secondary TTP and may be adopted as adjuvant therapy. Wolters Kluwer Health 2016-06-17 /pmc/articles/PMC4998437/ /pubmed/27310951 http://dx.doi.org/10.1097/MD.0000000000003712 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 3900
Nakamura, Kensuke
Inokuchi, Ryota
Hiruma, Takahiro
Ohshima, Kazuma
Sonoo, Tomohiro
Tokunaga, Kurato
Doi, Kent
Nakajima, Susumu
Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura
title Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura
title_full Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura
title_fullStr Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura
title_full_unstemmed Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura
title_short Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura
title_sort recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura
topic 3900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998437/
https://www.ncbi.nlm.nih.gov/pubmed/27310951
http://dx.doi.org/10.1097/MD.0000000000003712
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