Oral contraceptive use in women with poor anticoagulant response to activated protein C but not carrying the factor V Leiden mutation increases the risk of venous thrombosis

Summary The factor V Leiden mutation (FVL), associated with reduced sensitivity to activated Protein C (APC), is a risk factor for venous thromboembolism (VTE) and displays a strong interaction with oral contraceptives (OC). The aim of this study was to evaluate the risk of VTE in OC users with redu...

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Veröffentlicht in:Thrombosis and haemostasis 2004-04, Vol.91 (4), p.712-718
Hauptverfasser: Legnani, Cristina, Cini, Michela, Cosmi, Benilde, Mattarozzi, Silvia, Manto, Giuseppa Lo, Palareti, Gualtiero
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container_end_page 718
container_issue 4
container_start_page 712
container_title Thrombosis and haemostasis
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creator Legnani, Cristina
Cini, Michela
Cosmi, Benilde
Mattarozzi, Silvia
Manto, Giuseppa Lo
Palareti, Gualtiero
description Summary The factor V Leiden mutation (FVL), associated with reduced sensitivity to activated Protein C (APC), is a risk factor for venous thromboembolism (VTE) and displays a strong interaction with oral contraceptives (OC). The aim of this study was to evaluate the risk of VTE in OC users with reduced APC sensitivity unrelated to the FVL. APC sensitivity was measured by an original aPTT-based test (without sample pre-dilution in factor V-deficient plasma) in 195 women who suffered from VTE in reproductive age and in 487 healthy women with results being expressed as normalized ratio. Subjects with currently known clinically relevant thrombophilic alterations were excluded. APC normalized ratios were stratified into quartiles. The adjusted ORs of subjects in the lower quartile (≤0.90) was 2.46 (95%CI: 1.02–5.95). Of the 195 patients, 89 had suffered VTE during OC. The 181 healthy women who had used OC for at least 6 months in the two year period before presentation but who had stopped OC at least 3 months before blood sampling were considered OC users. The risk of VTE in subjects using OC with APC normalized ratio in the lower quartile was increased 4.9-fold (95% CI: 1.92–12.6). In conclusion, our results showed that altered APC resistance in women not carrying the FVL significantly increased the VTE risk, albeit to a lesser extent than in women also carrying the FVL. Our data also showed that OC use in women with altered APC resistance further increased the risk of VTE in a way that exceeded the additive expectation.
doi_str_mv 10.1160/TH03-10-0621
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The aim of this study was to evaluate the risk of VTE in OC users with reduced APC sensitivity unrelated to the FVL. APC sensitivity was measured by an original aPTT-based test (without sample pre-dilution in factor V-deficient plasma) in 195 women who suffered from VTE in reproductive age and in 487 healthy women with results being expressed as normalized ratio. Subjects with currently known clinically relevant thrombophilic alterations were excluded. APC normalized ratios were stratified into quartiles. The adjusted ORs of subjects in the lower quartile (≤0.90) was 2.46 (95%CI: 1.02–5.95). Of the 195 patients, 89 had suffered VTE during OC. The 181 healthy women who had used OC for at least 6 months in the two year period before presentation but who had stopped OC at least 3 months before blood sampling were considered OC users. The risk of VTE in subjects using OC with APC normalized ratio in the lower quartile was increased 4.9-fold (95% CI: 1.92–12.6). In conclusion, our results showed that altered APC resistance in women not carrying the FVL significantly increased the VTE risk, albeit to a lesser extent than in women also carrying the FVL. Our data also showed that OC use in women with altered APC resistance further increased the risk of VTE in a way that exceeded the additive expectation.</description><identifier>ISSN: 0340-6245</identifier><identifier>EISSN: 2567-689X</identifier><identifier>DOI: 10.1160/TH03-10-0621</identifier><identifier>PMID: 15045132</identifier><identifier>CODEN: THHADQ</identifier><language>eng</language><publisher>Stuttgart: Schattauer Verlag für Medizin und Naturwissenschaften</publisher><subject>Activated Protein C Resistance - complications ; Activated Protein C Resistance - drug therapy ; Adolescent ; Adult ; Anticoagulants - pharmacology ; Biological and medical sciences ; Blood Coagulation, Fibrinolysis and Cellular Haemostasis ; Blood coagulation. Blood cells ; Case-Control Studies ; Contraceptives, Oral - adverse effects ; Factor V ; Female ; Fundamental and applied biological sciences. Psychology ; Hematologic and hematopoietic diseases ; Humans ; Medical sciences ; Middle Aged ; Molecular and cellular biology ; Odds Ratio ; Platelet diseases and coagulopathies ; Risk ; Venous Thrombosis - chemically induced ; Venous Thrombosis - etiology</subject><ispartof>Thrombosis and haemostasis, 2004-04, Vol.91 (4), p.712-718</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c568t-3101ba575306807e1d1f163882d0355eff12fa9401f5e83bebf652ec8919af1a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH03-10-0621.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1160/TH03-10-0621$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3005,27901,27902,54534,54535</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15801697$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15045132$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Legnani, Cristina</creatorcontrib><creatorcontrib>Cini, Michela</creatorcontrib><creatorcontrib>Cosmi, Benilde</creatorcontrib><creatorcontrib>Mattarozzi, Silvia</creatorcontrib><creatorcontrib>Manto, Giuseppa Lo</creatorcontrib><creatorcontrib>Palareti, Gualtiero</creatorcontrib><title>Oral contraceptive use in women with poor anticoagulant response to activated protein C but not carrying the factor V Leiden mutation increases the risk of venous thrombosis</title><title>Thrombosis and haemostasis</title><addtitle>Thromb Haemost</addtitle><description>Summary The factor V Leiden mutation (FVL), associated with reduced sensitivity to activated Protein C (APC), is a risk factor for venous thromboembolism (VTE) and displays a strong interaction with oral contraceptives (OC). The aim of this study was to evaluate the risk of VTE in OC users with reduced APC sensitivity unrelated to the FVL. APC sensitivity was measured by an original aPTT-based test (without sample pre-dilution in factor V-deficient plasma) in 195 women who suffered from VTE in reproductive age and in 487 healthy women with results being expressed as normalized ratio. Subjects with currently known clinically relevant thrombophilic alterations were excluded. APC normalized ratios were stratified into quartiles. The adjusted ORs of subjects in the lower quartile (≤0.90) was 2.46 (95%CI: 1.02–5.95). Of the 195 patients, 89 had suffered VTE during OC. The 181 healthy women who had used OC for at least 6 months in the two year period before presentation but who had stopped OC at least 3 months before blood sampling were considered OC users. The risk of VTE in subjects using OC with APC normalized ratio in the lower quartile was increased 4.9-fold (95% CI: 1.92–12.6). In conclusion, our results showed that altered APC resistance in women not carrying the FVL significantly increased the VTE risk, albeit to a lesser extent than in women also carrying the FVL. Our data also showed that OC use in women with altered APC resistance further increased the risk of VTE in a way that exceeded the additive expectation.</description><subject>Activated Protein C Resistance - complications</subject><subject>Activated Protein C Resistance - drug therapy</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Anticoagulants - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Blood Coagulation, Fibrinolysis and Cellular Haemostasis</subject><subject>Blood coagulation. Blood cells</subject><subject>Case-Control Studies</subject><subject>Contraceptives, Oral - adverse effects</subject><subject>Factor V</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular and cellular biology</subject><subject>Odds Ratio</subject><subject>Platelet diseases and coagulopathies</subject><subject>Risk</subject><subject>Venous Thrombosis - chemically induced</subject><subject>Venous Thrombosis - etiology</subject><issn>0340-6245</issn><issn>2567-689X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqtkUFv1DAQhSMEokvhxhn5wgkCdhw7yRFVhSKt1EtB3KyJM25cEjuynVb9UfxHHHZFERI3LrbH_uY9-U1RvGT0HWOSvr-6oLxktKSyYo-KXSVkU8q2-_a42FFe01JWtTgpnsV4QymTdSeeFidM0FowXu2KH5cBJqK9SwE0LsneIlkjEuvInZ8xrzaNZPE-EHDJag_X65RPJGBcvMtk8gR07oOEA1mCT5h7z0i_JuJ8IhpCuLfumqQRiclkVvpK9miHLD6vCZL1LtvpgBAx_sKCjd-JN-QWnV-3q-Dn3kcbnxdPDEwRXxz30-LLx_Ors4tyf_np89mHfamFbFPJGWU9iEZwKlvaIBuYYZK3bTVQLgQawyoDXU2ZEdjyHnsjRYW67VgHhgE_Ld4edHXwMQY0agl2hnCvGFVb6mpLfSu21DP-6oAvaz_j8AAfY87A6yMAUcNkAjht4x9cm0fTNZl7c-DSaHFGdePX4PJH_2WrD3TUI6QEK4bfkg-ZKXCDGgFnHxNs9TZsdCk_BD3meSsb44oqLqgtTGoGt0Yd7JIUb1idXex_dGka-beDiqO_U2OaJ_4TrbHsyQ</recordid><startdate>20040401</startdate><enddate>20040401</enddate><creator>Legnani, Cristina</creator><creator>Cini, Michela</creator><creator>Cosmi, Benilde</creator><creator>Mattarozzi, Silvia</creator><creator>Manto, Giuseppa Lo</creator><creator>Palareti, Gualtiero</creator><general>Schattauer Verlag für Medizin und Naturwissenschaften</general><general>Schattauer GmbH</general><general>Schattauer</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20040401</creationdate><title>Oral contraceptive use in women with poor anticoagulant response to activated protein C but not carrying the factor V Leiden mutation increases the risk of venous thrombosis</title><author>Legnani, Cristina ; Cini, Michela ; Cosmi, Benilde ; Mattarozzi, Silvia ; Manto, Giuseppa Lo ; Palareti, Gualtiero</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c568t-3101ba575306807e1d1f163882d0355eff12fa9401f5e83bebf652ec8919af1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Activated Protein C Resistance - complications</topic><topic>Activated Protein C Resistance - drug therapy</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Anticoagulants - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Blood Coagulation, Fibrinolysis and Cellular Haemostasis</topic><topic>Blood coagulation. Blood cells</topic><topic>Case-Control Studies</topic><topic>Contraceptives, Oral - adverse effects</topic><topic>Factor V</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molecular and cellular biology</topic><topic>Odds Ratio</topic><topic>Platelet diseases and coagulopathies</topic><topic>Risk</topic><topic>Venous Thrombosis - chemically induced</topic><topic>Venous Thrombosis - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Legnani, Cristina</creatorcontrib><creatorcontrib>Cini, Michela</creatorcontrib><creatorcontrib>Cosmi, Benilde</creatorcontrib><creatorcontrib>Mattarozzi, Silvia</creatorcontrib><creatorcontrib>Manto, Giuseppa Lo</creatorcontrib><creatorcontrib>Palareti, Gualtiero</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Legnani, Cristina</au><au>Cini, Michela</au><au>Cosmi, Benilde</au><au>Mattarozzi, Silvia</au><au>Manto, Giuseppa Lo</au><au>Palareti, Gualtiero</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral contraceptive use in women with poor anticoagulant response to activated protein C but not carrying the factor V Leiden mutation increases the risk of venous thrombosis</atitle><jtitle>Thrombosis and haemostasis</jtitle><addtitle>Thromb Haemost</addtitle><date>2004-04-01</date><risdate>2004</risdate><volume>91</volume><issue>4</issue><spage>712</spage><epage>718</epage><pages>712-718</pages><issn>0340-6245</issn><eissn>2567-689X</eissn><coden>THHADQ</coden><abstract>Summary The factor V Leiden mutation (FVL), associated with reduced sensitivity to activated Protein C (APC), is a risk factor for venous thromboembolism (VTE) and displays a strong interaction with oral contraceptives (OC). The aim of this study was to evaluate the risk of VTE in OC users with reduced APC sensitivity unrelated to the FVL. APC sensitivity was measured by an original aPTT-based test (without sample pre-dilution in factor V-deficient plasma) in 195 women who suffered from VTE in reproductive age and in 487 healthy women with results being expressed as normalized ratio. Subjects with currently known clinically relevant thrombophilic alterations were excluded. APC normalized ratios were stratified into quartiles. The adjusted ORs of subjects in the lower quartile (≤0.90) was 2.46 (95%CI: 1.02–5.95). Of the 195 patients, 89 had suffered VTE during OC. The 181 healthy women who had used OC for at least 6 months in the two year period before presentation but who had stopped OC at least 3 months before blood sampling were considered OC users. The risk of VTE in subjects using OC with APC normalized ratio in the lower quartile was increased 4.9-fold (95% CI: 1.92–12.6). In conclusion, our results showed that altered APC resistance in women not carrying the FVL significantly increased the VTE risk, albeit to a lesser extent than in women also carrying the FVL. Our data also showed that OC use in women with altered APC resistance further increased the risk of VTE in a way that exceeded the additive expectation.</abstract><cop>Stuttgart</cop><pub>Schattauer Verlag für Medizin und Naturwissenschaften</pub><pmid>15045132</pmid><doi>10.1160/TH03-10-0621</doi><tpages>7</tpages></addata></record>
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ispartof Thrombosis and haemostasis, 2004-04, Vol.91 (4), p.712-718
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source MEDLINE; Thieme Connect Journals
subjects Activated Protein C Resistance - complications
Activated Protein C Resistance - drug therapy
Adolescent
Adult
Anticoagulants - pharmacology
Biological and medical sciences
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Blood coagulation. Blood cells
Case-Control Studies
Contraceptives, Oral - adverse effects
Factor V
Female
Fundamental and applied biological sciences. Psychology
Hematologic and hematopoietic diseases
Humans
Medical sciences
Middle Aged
Molecular and cellular biology
Odds Ratio
Platelet diseases and coagulopathies
Risk
Venous Thrombosis - chemically induced
Venous Thrombosis - etiology
title Oral contraceptive use in women with poor anticoagulant response to activated protein C but not carrying the factor V Leiden mutation increases the risk of venous thrombosis
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