Suppr超能文献

血浆因子和抑制剂组成影响急性或既往脑血管事件患者的凝血酶生成动力学。

Plasma factor and inhibitor composition contributes to thrombin generation dynamics in patients with acute or previous cerebrovascular events.

机构信息

Department of Biochemistry, University of Vermont, Colchester, VT, USA.

出版信息

Thromb Res. 2010 Oct;126(4):262-9. doi: 10.1016/j.thromres.2010.07.002. Epub 2010 Aug 14.

Abstract

INTRODUCTION

More than 80% of cerebrovascular events are ischemic and largely thromboembolic by nature. We evaluated whether plasma factor composition and thrombin generation dynamics might be a contributor to the thrombotic phenotype of ischemic cerebrovascular events.

MATERIALS AND METHODS

We studied (1) 100 patients with acute ischemic stroke (n=50) or transient ischemic attack (TIA) (n=50) within the first 24 hours from symptom onset, and (2) 100 individuals 1 to 4 years following ischemic stroke (n=50) or TIA (n=50). The tissue factor pathway to thrombin generation was simulated with a mathematical model using plasma levels of clotting factors (F)II, V, VII, VIII, IX, X, antithrombin and free tissue factor pathway inhibitor (TFPI).

RESULTS

The plasma levels of free TFPI, FII, FVIII, and FX were higher, while antithrombin was lower, in the acute patients compared to the previous event group (all p≤0.02). Thrombin generation during acute events was enhanced, with an 11% faster maximum rate, a 15% higher maximum level and a 26% larger total production (all p<0.01). The increased thrombin generation in acute patients was determined by higher FII and lower antithrombin, while increased free TFPI mediated this effect. When the groups are classified by etiology, all stroke sub-types except cardioembolic have increased TFPI and decreased AT and total thrombin produced.

CONCLUSION

Augmented thrombin generation in acute stroke/TIA is to some extent determined by altered plasma levels of coagulation factors.

摘要

简介

超过 80%的脑血管事件为缺血性,且本质上大多为血栓栓塞性。我们评估了血浆因子组成和凝血酶生成动力学是否可能是缺血性脑血管事件血栓表型的一个促成因素。

材料与方法

我们研究了(1)发病后 24 小时内的 100 例急性缺血性脑卒中(n=50)或短暂性脑缺血发作(TIA)(n=50)患者,以及(2)缺血性脑卒中(n=50)或 TIA(n=50)后 1 至 4 年的 100 例个体。使用数学模型模拟组织因子途径向凝血酶生成,该模型使用血浆中凝血因子(F)II、V、VII、VIII、IX、X、抗凝血酶和游离组织因子途径抑制剂(TFPI)的水平。

结果

与前一次事件组相比,急性患者的血浆游离 TFPI、FII、FVIII 和 FX 水平更高,而抗凝血酶水平更低(均 p≤0.02)。急性事件期间的凝血酶生成增强,最大速率快 11%,最大水平高 15%,总生成量高 26%(均 p<0.01)。急性患者的凝血酶生成增加是由 FII 升高和抗凝血酶降低引起的,而游离 TFPI 的增加介导了这种作用。当按病因对组进行分类时,除心源性栓塞外的所有脑卒中亚型均增加了 TFPI,降低了 AT 和总凝血酶的产生。

结论

急性脑卒中/TIA 中凝血酶生成的增加在一定程度上是由凝血因子血浆水平的改变决定的。

相似文献

2
Thrombin generation in chronic obstructive pulmonary disease: dependence on plasma factor composition.
Thromb Res. 2011 Oct;128(4):e24-8. doi: 10.1016/j.thromres.2011.05.004. Epub 2011 May 31.
3
Thrombin generation in rheumatoid arthritis: dependence on plasma factor composition.
Thromb Haemost. 2010 Aug;104(2):224-30. doi: 10.1160/TH10-02-0091. Epub 2010 Jun 30.
4
"Normal" thrombin generation.
Blood. 1999 Oct 1;94(7):2169-78.
9
Thrombin generation in acute coronary syndrome and stable coronary artery disease: dependence on plasma factor composition.
J Thromb Haemost. 2008 Jan;6(1):104-10. doi: 10.1111/j.1538-7836.2007.02799.x. Epub 2007 Oct 15.

引用本文的文献

1
Systems Biology Approach for Personalized Hemostasis Correction.
J Pers Med. 2022 Nov 15;12(11):1903. doi: 10.3390/jpm12111903.
2
Mathematical model of thrombin generation and bleeding phenotype in Amish carriers of Factor IX:C deficiency vs. controls.
Thromb Res. 2019 Oct;182:43-50. doi: 10.1016/j.thromres.2019.07.020. Epub 2019 Aug 8.
3
In silico thrombin generation: Plasma composition imbalance and mortality in human immunodeficiency virus.
Res Pract Thromb Haemost. 2018 Sep 11;2(4):708-717. doi: 10.1002/rth2.12147. eCollection 2018 Oct.
4
Low thrombin generation predicts poor prognosis in ischemic stroke patients after thrombolysis.
PLoS One. 2017 Jul 10;12(7):e0180477. doi: 10.1371/journal.pone.0180477. eCollection 2017.
5
Modeling thrombin generation: plasma composition based approach.
J Thromb Thrombolysis. 2014 Jan;37(1):32-44. doi: 10.1007/s11239-013-1006-9.
7
Factor Xa generation by computational modeling: an additional discriminator to thrombin generation evaluation.
PLoS One. 2012;7(1):e29178. doi: 10.1371/journal.pone.0029178. Epub 2012 Jan 11.
8
The influence of prophylactic factor VIII in severe haemophilia A.
Haemophilia. 2012 Mar;18(2):193-9. doi: 10.1111/j.1365-2516.2011.02638.x. Epub 2011 Sep 7.

本文引用的文献

1
Peak thrombin generation and subsequent venous thromboembolism: the Longitudinal Investigation of Thromboembolism Etiology (LITE) study.
J Thromb Haemost. 2009 Oct;7(10):1639-48. doi: 10.1111/j.1538-7836.2009.03561.x. Epub 2009 Jul 28.
2
Empirical and theoretical phenotypic discrimination.
J Thromb Haemost. 2009 Jul;7 Suppl 1(Suppl 1):181-6. doi: 10.1111/j.1538-7836.2009.03426.x.
4
The effect of high circulating estradiol levels on thrombin generation during in vitro fertilization.
Thromb Res. 2009 Sep;124(4):505-7. doi: 10.1016/j.thromres.2009.02.006. Epub 2009 Mar 17.
5
Thrombin generation in acute coronary syndrome and stable coronary artery disease: dependence on plasma factor composition.
J Thromb Haemost. 2008 Jan;6(1):104-10. doi: 10.1111/j.1538-7836.2007.02799.x. Epub 2007 Oct 15.
6
Thrombin activatable fibrinolysis inhibitor activation peptide shows association with all major subtypes of ischemic stroke and with TAFI gene variation.
Arterioscler Thromb Vasc Biol. 2007 Apr;27(4):955-62. doi: 10.1161/01.ATV.0000259354.93789.a6. Epub 2007 Feb 1.
7
The tissue factor pathway in ischemic stroke.
Blood Coagul Fibrinolysis. 2006 Oct;17(7):527-32. doi: 10.1097/01.mbc.0000245294.41774.06.
9
Hypercoagulable states and strokes.
Curr Atheroscler Rep. 2006 Jul;8(4):324-9. doi: 10.1007/s11883-006-0011-2.
10
Thrombin generation profiles in deep venous thrombosis.
J Thromb Haemost. 2005 Nov;3(11):2497-505. doi: 10.1111/j.1538-7836.2005.01584.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验