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Recombinant thrombomodulin for secondary thrombotic thrombocytopenic purpura

机译:重组血栓调节蛋白治疗继发性血栓性血小板减少性紫癜

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摘要

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 x 10(3)/mu L); 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 (x 1000/mu L) (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.
机译:在血栓性血小板减少性紫癜(TTP)的发病机理中,ADAMTS13的酶活性降低会切割超大型von Willebrand多聚体,在微血管内皮上产生剪切应力,从而导致血小板聚集和血栓形成。在典型的TTP中,ADAMTS13活性显着降低,但在继发性TTP中仅轻度降低,继发性TTP与原发性疾病同时发展。后者随着败血性弥散性血管内凝血(DIC)的发展而发展,并经常引起器官衰竭。重组血栓调节蛋白(rTM)是一种用于治疗DIC的药物,也可以缓解TTP,因为它可以改善血管内皮功能障碍。因此,我们在本文中研究了rTM在继发性TTP病理学治疗的患者中的疗效。提取并回顾性分析入院急诊中心的患者并进行回顾性分析:溶血性贫血伴红细胞破碎(Hb <12 g / dL或更低);血小板减少症(<100 x 10(3)/μL);并且ADAMTS13活性<50%。纳入16例患者,并伴有“肾脏疾病:改善总体预后”(KDIGO)2期或更严重的肾病和DIC。比较了使用rTM和不使用rTM的11例和5例患者(分别为rTM和非rTM治疗组),并且在基本特征(例如背景疾病和严重程度)上未发现明显差异。存活率无明显差异。然而,血小板计数是TTP治疗的重要结果,在rTM治疗组中显着增加:3.3 +/- 2.6-> 11.3 +/- 14.6与3.5 +/- 3.7-> 5.7 +/- 3.9( ×1000 /μL)(P = 0.034)。血栓性血小板减少性紫癜最初需要侵入性治疗,其预后并不理想。血液中血栓调节蛋白水平也由于血管内皮功能障碍而明显增加,而rTM可以缓解高TM血液水平的TTP患者的血管内皮功能障碍,这表明使用rTM的重要性。因此,rTM对于继发性TTP可能是有效的,并且可以被用作辅助治疗。

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