{"title":"开始联合口服避孕药三个月后接触系统活性增加。","authors":"Jesper Strandberg, Jette Nybo, Inger Lise Gade, Yaseelan Palarasah, Else-Marie Bladbjerg, Søren Risom Kristensen","doi":"10.1016/j.thromres.2025.109428","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Combined oral contraceptives (COC) are associated with an increased risk of venous thromboembolism (VTE). The contact system (CAS) can, when activated, stimulate coagulation, and may play a role in thrombus formation. Our recent case-control study showed increased CAS capacity and in vivo activity in COC users, indicating a systemic activation that could contribute to VTE risk during COC treatment. Aim This study investigates intraindividual changes in CAS in women before and after start of COC treatment.</p><p><strong>Materials and methods: </strong>Twenty-four women aged between 15 and 34 years, who were starting treatment with COC, were included in the study. A baseline blood sample was drawn before start of COC, and a follow-up blood sample 3-4 months later. The capacity and activity of CAS, i.e. factor XII (FXII), prekallikrein (PK), H-kininogen (HK), C1-esterase inhibitor (C1inh), cleaved HK (cHK) and endogenous kallikrein potential (EKP), were analyzed.</p><p><strong>Results: </strong>Our study showed significantly increased levels of FXII (median 29.4 vs 42.9 mg/L; p < 0.0001) and decreased levels of C1inh (0.21 vs 0.20 g/L; p = 0.005). Increased EKP (1859 vs 2203 nmol/L*min; p = 0.0004) demonstrated an increased capacity of CAS, and increased levels of cHK (0.70 vs 0.96 μg/L; p < 0.0001) indicated an increased activity of CAS in vivo. The levels of PK and HK showed no significant changes.</p><p><strong>Conclusion: </strong>This study demonstrates an increased intraindividual CAS capacity as well as an increased CAS activity during treatment with COC supporting the previous research. These effects on CAS may contribute to the increased thrombotic risk caused by COC.</p>","PeriodicalId":23064,"journal":{"name":"Thrombosis research","volume":"253 ","pages":"109428"},"PeriodicalIF":3.4000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Increased contact system activity three months after starting combined oral contraceptives.\",\"authors\":\"Jesper Strandberg, Jette Nybo, Inger Lise Gade, Yaseelan Palarasah, Else-Marie Bladbjerg, Søren Risom Kristensen\",\"doi\":\"10.1016/j.thromres.2025.109428\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Combined oral contraceptives (COC) are associated with an increased risk of venous thromboembolism (VTE). The contact system (CAS) can, when activated, stimulate coagulation, and may play a role in thrombus formation. Our recent case-control study showed increased CAS capacity and in vivo activity in COC users, indicating a systemic activation that could contribute to VTE risk during COC treatment. Aim This study investigates intraindividual changes in CAS in women before and after start of COC treatment.</p><p><strong>Materials and methods: </strong>Twenty-four women aged between 15 and 34 years, who were starting treatment with COC, were included in the study. A baseline blood sample was drawn before start of COC, and a follow-up blood sample 3-4 months later. The capacity and activity of CAS, i.e. factor XII (FXII), prekallikrein (PK), H-kininogen (HK), C1-esterase inhibitor (C1inh), cleaved HK (cHK) and endogenous kallikrein potential (EKP), were analyzed.</p><p><strong>Results: </strong>Our study showed significantly increased levels of FXII (median 29.4 vs 42.9 mg/L; p < 0.0001) and decreased levels of C1inh (0.21 vs 0.20 g/L; p = 0.005). Increased EKP (1859 vs 2203 nmol/L*min; p = 0.0004) demonstrated an increased capacity of CAS, and increased levels of cHK (0.70 vs 0.96 μg/L; p < 0.0001) indicated an increased activity of CAS in vivo. The levels of PK and HK showed no significant changes.</p><p><strong>Conclusion: </strong>This study demonstrates an increased intraindividual CAS capacity as well as an increased CAS activity during treatment with COC supporting the previous research. 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引用次数: 0
摘要
联合口服避孕药(COC)与静脉血栓栓塞(VTE)的风险增加有关。当接触系统(CAS)被激活时,可以刺激凝血,并可能在血栓形成中发挥作用。我们最近的病例对照研究显示,COC使用者的CAS容量和体内活性增加,表明COC治疗期间,系统激活可能增加静脉血栓栓塞风险。目的探讨COC治疗开始前后女性CAS的个体变化。材料和方法:24名年龄在15至34岁之间,开始接受COC治疗的女性纳入研究。在COC开始前抽取基线血液样本,并在3-4个月后抽取随访血液样本。分析了CAS的容量和活性,即因子XII (FXII)、预激钾素(PK)、h -激钾素原(HK)、c1酯酶抑制剂(C1inh)、裂解型HK (cHK)和内源性激钾素电位(EKP)。结果:我们的研究显示FXII水平显著升高(中位数为29.4 vs 42.9 mg/L;结论:本研究表明,在COC治疗期间,个体内CAS容量增加,CAS活性增加,支持先前的研究。这些对CAS的影响可能导致COC引起的血栓形成风险增加。
Increased contact system activity three months after starting combined oral contraceptives.
Introduction: Combined oral contraceptives (COC) are associated with an increased risk of venous thromboembolism (VTE). The contact system (CAS) can, when activated, stimulate coagulation, and may play a role in thrombus formation. Our recent case-control study showed increased CAS capacity and in vivo activity in COC users, indicating a systemic activation that could contribute to VTE risk during COC treatment. Aim This study investigates intraindividual changes in CAS in women before and after start of COC treatment.
Materials and methods: Twenty-four women aged between 15 and 34 years, who were starting treatment with COC, were included in the study. A baseline blood sample was drawn before start of COC, and a follow-up blood sample 3-4 months later. The capacity and activity of CAS, i.e. factor XII (FXII), prekallikrein (PK), H-kininogen (HK), C1-esterase inhibitor (C1inh), cleaved HK (cHK) and endogenous kallikrein potential (EKP), were analyzed.
Results: Our study showed significantly increased levels of FXII (median 29.4 vs 42.9 mg/L; p < 0.0001) and decreased levels of C1inh (0.21 vs 0.20 g/L; p = 0.005). Increased EKP (1859 vs 2203 nmol/L*min; p = 0.0004) demonstrated an increased capacity of CAS, and increased levels of cHK (0.70 vs 0.96 μg/L; p < 0.0001) indicated an increased activity of CAS in vivo. The levels of PK and HK showed no significant changes.
Conclusion: This study demonstrates an increased intraindividual CAS capacity as well as an increased CAS activity during treatment with COC supporting the previous research. These effects on CAS may contribute to the increased thrombotic risk caused by COC.
期刊介绍:
Thrombosis Research is an international journal dedicated to the swift dissemination of new information on thrombosis, hemostasis, and vascular biology, aimed at advancing both science and clinical care. The journal publishes peer-reviewed original research, reviews, editorials, opinions, and critiques, covering both basic and clinical studies. Priority is given to research that promises novel approaches in the diagnosis, therapy, prognosis, and prevention of thrombotic and hemorrhagic diseases.