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Plasma Kallikrein Cleaved H-kininogen: An End-Point Marker for Contact Activation and .血浆激肽释放酶裂解的H-激肽原:接触激活的终点标志物及…… (原文最后不完整)
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2
Thrombin generation measured on ST Genesia, a new platform in the coagulation routine lab: Assessment of analytical and between-subject variation.在凝血常规实验室的新平台ST Genesia上进行的凝血酶生成检测:分析性变异和受试者间变异的评估。
Res Pract Thromb Haemost. 2022 Jan 31;6(1):e12654. doi: 10.1002/rth2.12654. eCollection 2022 Jan.
3
High Molecular Weight Kininogen: A Review of the Structural Literature.高分子量激肽原:结构文献综述。
Int J Mol Sci. 2021 Dec 13;22(24):13370. doi: 10.3390/ijms222413370.
4
An update on factor XII-driven vascular inflammation.关于因子 XII 驱动的血管炎症的最新进展。
Biochim Biophys Acta Mol Cell Res. 2022 Jan;1869(1):119166. doi: 10.1016/j.bbamcr.2021.119166. Epub 2021 Oct 24.
5
Polyphosphate expression by cancer cell extracellular vesicles mediates binding of factor XII and contact activation.癌细胞细胞外囊泡表达多磷酸盐介导凝血因子 XII 的结合和接触激活。
Blood Adv. 2021 Nov 23;5(22):4741-4751. doi: 10.1182/bloodadvances.2021005116.
6
Factor XII(a) inhibitors: a review of the patent literature.因子 XII(a)抑制剂:专利文献综述。
Expert Opin Ther Pat. 2021 Dec;31(12):1155-1176. doi: 10.1080/13543776.2021.1945580. Epub 2021 Jul 27.
7
The contact system in liver injury.肝脏损伤中的接触系统。
Semin Immunopathol. 2021 Aug;43(4):507-517. doi: 10.1007/s00281-021-00876-7. Epub 2021 Jun 14.
8
Effect of Anabolic-Androgenic Steroid Abuse on the Contact Activation System.滥用合成代谢雄激素类固醇对接触激活系统的影响。
Thromb Haemost. 2021 Oct;121(10):1268-1273. doi: 10.1055/a-1346-3384. Epub 2021 Feb 28.
9
Proteolytic activity of contact factor zymogens.接触因子酶原的蛋白水解活性。
J Thromb Haemost. 2021 Feb;19(2):330-341. doi: 10.1111/jth.15149. Epub 2020 Dec 7.
10
The rebirth of the contact pathway: a new therapeutic target.接触途径的重生:一个新的治疗靶点。
Curr Opin Hematol. 2020 Sep;27(5):311-319. doi: 10.1097/MOH.0000000000000603.

复方口服避孕药可能会激活健康女性的接触系统。

Combined oral contraceptives may activate the contact system in healthy women.

作者信息

Strandberg Jesper, Gade Inger Lise, Palarasah Yaseelan, Gram Jørgen Brodersen, Kristensen Søren Risom, Sidelmann Johannes Jakobsen

机构信息

Department of Clinical Biochemistry, The Coagulation Unit, Aalborg University Hospital, Aalborg, Denmark.

Department of Haematology and Clinical Cancer Research Centre, Aalborg University Hospital, Aalborg, Denmark.

出版信息

Res Pract Thromb Haemost. 2023 Mar 13;7(2):100118. doi: 10.1016/j.rpth.2023.100118. eCollection 2023 Feb.

DOI:10.1016/j.rpth.2023.100118
PMID:37063763
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10099323/
Abstract

BACKGROUND

The contact system (CAS) is part of the coagulation system, consisting of a group of plasma proteins stimulating inflammation, coagulation, and fibrinolysis when activated. CAS can be triggered by several activating surfaces, and CAS may play a potential role in thrombus formation. Combined oral contraceptives (COCs) are known to increase the risk of venous thromboembolism, and COCs induce various prothrombotic changes in the coagulation system, whereas the effect of COC on CAS has not been thoroughly investigated.

OBJECTIVES

To investigate CAS in COC users compared with nonusers.

METHODS

Blood samples from 62 study subjects, 30 COC users, and 32 nonusers, were analyzed. Coagulation factor XII (FXII), prekallikrein (PK), H-Kininogen (HK), cleaved HK (cHK), C1-esterase inhibitor (C1-inh), and the endogenous kallikrein potential (EKP) were measured.

RESULTS

COC users had significantly higher FXII (median, 38.4 vs 28.9 mg/L) and lower C1-inh levels (0.20 vs 0.23 g/L) than nonusers. The levels of PK and HK were not significantly different. Measurement of EKP indicated an increased capacity of CAS in COC users (1860 vs 1500 nmol/L × min), and increased plasma levels of cHK (2.02 vs 1.07 μg/L) indicated an increased activity .

CONCLUSION

This study demonstrates an increased CAS capacity in women using COC compared with nonusers and also an increased activity . The results indicate that increased contact activation may contribute to the increased thrombotic risk caused by COC.

摘要

背景

接触系统(CAS)是凝血系统的一部分,由一组血浆蛋白组成,激活时会刺激炎症、凝血和纤维蛋白溶解。CAS可由多种激活表面触发,可能在血栓形成中发挥潜在作用。已知复方口服避孕药(COC)会增加静脉血栓栓塞的风险,COC会在凝血系统中引起各种促血栓形成变化,而COC对CAS的影响尚未得到充分研究。

目的

比较使用COC的女性与未使用者的CAS情况。

方法

分析了62名研究对象的血样,其中30名COC使用者和32名未使用者。测量了凝血因子XII(FXII)、前激肽释放酶(PK)、H-激肽原(HK)、裂解的HK(cHK)、C1酯酶抑制剂(C1-inh)和内源性激肽释放酶潜力(EKP)。

结果

与未使用者相比,COC使用者的FXII水平显著更高(中位数,38.4对28.9mg/L),C1-inh水平更低(0.20对0.23g/L)。PK和HK水平无显著差异。EKP测量表明COC使用者的CAS能力增强(1860对1500nmol/L×min),cHK血浆水平升高(2.02对1.07μg/L)表明活性增加。

结论

本研究表明,与未使用者相比,使用CO使用COC的女性CAS能力增强,活性也增加。结果表明,接触激活增加可能导致COC引起的血栓形成风险增加。