Combined oral contraceptives may activate the contact system in healthy women
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 con...
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Veröffentlicht in: | Research and practice in thrombosis and haemostasis 2023-02, Vol.7 (2), p.100118-100118, Article 100118 |
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description | 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.
To investigate CAS in COC users compared with nonusers.
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.
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 in vivo.
This study demonstrates an increased CAS capacity in women using COC compared with nonusers and also an increased activity in vivo. The results indicate that increased contact activation may contribute to the increased thrombotic risk caused by COC.
•The contact system (CAS) may play a potential role in thrombus formation•Methods have been developed to measure the capacity and activity of CAS•CAS capacity is increased in women using combined oral contraceptives (COCs) (birth-control pills)•Increased CAS capacity may contribute to the increased thrombotic risk caused by COC |
doi_str_mv | 10.1016/j.rpth.2023.100118 |
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To investigate CAS in COC users compared with nonusers.
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.
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 in vivo.
This study demonstrates an increased CAS capacity in women using COC compared with nonusers and also an increased activity in vivo. The results indicate that increased contact activation may contribute to the increased thrombotic risk caused by COC.
•The contact system (CAS) may play a potential role in thrombus formation•Methods have been developed to measure the capacity and activity of CAS•CAS capacity is increased in women using combined oral contraceptives (COCs) (birth-control pills)•Increased CAS capacity may contribute to the increased thrombotic risk caused by COC</description><identifier>ISSN: 2475-0379</identifier><identifier>EISSN: 2475-0379</identifier><identifier>DOI: 10.1016/j.rpth.2023.100118</identifier><identifier>PMID: 37063763</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>combined oral contraceptives ; complement C1 inhibitor protein ; contact system ; endogenous kallikrein potential ; factor XII ; Original</subject><ispartof>Research and practice in thrombosis and haemostasis, 2023-02, Vol.7 (2), p.100118-100118, Article 100118</ispartof><rights>2023 The Authors</rights><rights>2023 The Authors.</rights><rights>2023 The Authors 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-941c245a6b9b2ea30d99e4fbbe17ce887e23e1d8f3b6255c2a9fe662d04b8a893</citedby><cites>FETCH-LOGICAL-c456t-941c245a6b9b2ea30d99e4fbbe17ce887e23e1d8f3b6255c2a9fe662d04b8a893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099323/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099323/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37063763$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Strandberg, Jesper</creatorcontrib><creatorcontrib>Gade, Inger Lise</creatorcontrib><creatorcontrib>Palarasah, Yaseelan</creatorcontrib><creatorcontrib>Gram, Jørgen Brodersen</creatorcontrib><creatorcontrib>Kristensen, Søren Risom</creatorcontrib><creatorcontrib>Sidelmann, Johannes Jakobsen</creatorcontrib><title>Combined oral contraceptives may activate the contact system in healthy women</title><title>Research and practice in thrombosis and haemostasis</title><addtitle>Res Pract Thromb Haemost</addtitle><description>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.
To investigate CAS in COC users compared with nonusers.
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.
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 in vivo.
This study demonstrates an increased CAS capacity in women using COC compared with nonusers and also an increased activity in vivo. The results indicate that increased contact activation may contribute to the increased thrombotic risk caused by COC.
•The contact system (CAS) may play a potential role in thrombus formation•Methods have been developed to measure the capacity and activity of CAS•CAS capacity is increased in women using combined oral contraceptives (COCs) (birth-control pills)•Increased CAS capacity may contribute to the increased thrombotic risk caused by COC</description><subject>combined oral contraceptives</subject><subject>complement C1 inhibitor protein</subject><subject>contact system</subject><subject>endogenous kallikrein potential</subject><subject>factor XII</subject><subject>Original</subject><issn>2475-0379</issn><issn>2475-0379</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9UU1LAzEQDaLYUvsHPEiOXlrzsV8BQaT4BRUveg7Z7KybsrupSVrpvze1tehFGJhh5s2b4T2EzimZUkKzq8XULUMzZYTx2CCUFkdoyJI8nRCei-Nf9QCNvV8QQiI2RnqKBjwnGc8zPkTPM9uVpocKW6darG0fnNKwDGYNHndqg5WOtQqAQwPf89jAfuMDdNj0uAHVhmaDP20H_Rk6qVXrYbzPI_R2f_c6e5zMXx6eZrfziU7SLExEQjVLUpWVomSgOKmEgKQuS6C5hqLIgXGgVVHzMmNpqpkSNWQZq0hSFqoQfIRudrzLVdlBpWH7dSuXznTKbaRVRv6d9KaR73Yto1JCcMYjw-WewdmPFfggO-M1tK3qwa68ZAVhCSsYSSOU7aDaWe8d1Ic7lMitF3Iht17IrRdy50Vcuvj94WHlR_kIuN4BIOq0NuCk1wZ6DZVxoIOsrPmP_wtNWZxc</recordid><startdate>20230201</startdate><enddate>20230201</enddate><creator>Strandberg, Jesper</creator><creator>Gade, Inger Lise</creator><creator>Palarasah, Yaseelan</creator><creator>Gram, Jørgen Brodersen</creator><creator>Kristensen, Søren Risom</creator><creator>Sidelmann, Johannes Jakobsen</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20230201</creationdate><title>Combined oral contraceptives may activate the contact system in healthy women</title><author>Strandberg, Jesper ; Gade, Inger Lise ; Palarasah, Yaseelan ; Gram, Jørgen Brodersen ; Kristensen, Søren Risom ; Sidelmann, Johannes Jakobsen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-941c245a6b9b2ea30d99e4fbbe17ce887e23e1d8f3b6255c2a9fe662d04b8a893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>combined oral contraceptives</topic><topic>complement C1 inhibitor protein</topic><topic>contact system</topic><topic>endogenous kallikrein potential</topic><topic>factor XII</topic><topic>Original</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Strandberg, Jesper</creatorcontrib><creatorcontrib>Gade, Inger Lise</creatorcontrib><creatorcontrib>Palarasah, Yaseelan</creatorcontrib><creatorcontrib>Gram, Jørgen Brodersen</creatorcontrib><creatorcontrib>Kristensen, Søren Risom</creatorcontrib><creatorcontrib>Sidelmann, Johannes Jakobsen</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Research and practice in thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Strandberg, Jesper</au><au>Gade, Inger Lise</au><au>Palarasah, Yaseelan</au><au>Gram, Jørgen Brodersen</au><au>Kristensen, Søren Risom</au><au>Sidelmann, Johannes Jakobsen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combined oral contraceptives may activate the contact system in healthy women</atitle><jtitle>Research and practice in thrombosis and haemostasis</jtitle><addtitle>Res Pract Thromb Haemost</addtitle><date>2023-02-01</date><risdate>2023</risdate><volume>7</volume><issue>2</issue><spage>100118</spage><epage>100118</epage><pages>100118-100118</pages><artnum>100118</artnum><issn>2475-0379</issn><eissn>2475-0379</eissn><abstract>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.
To investigate CAS in COC users compared with nonusers.
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.
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 in vivo.
This study demonstrates an increased CAS capacity in women using COC compared with nonusers and also an increased activity in vivo. The results indicate that increased contact activation may contribute to the increased thrombotic risk caused by COC.
•The contact system (CAS) may play a potential role in thrombus formation•Methods have been developed to measure the capacity and activity of CAS•CAS capacity is increased in women using combined oral contraceptives (COCs) (birth-control pills)•Increased CAS capacity may contribute to the increased thrombotic risk caused by COC</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>37063763</pmid><doi>10.1016/j.rpth.2023.100118</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | combined oral contraceptives complement C1 inhibitor protein contact system endogenous kallikrein potential factor XII Original |
title | Combined oral contraceptives may activate the contact system in healthy women |
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