Prothrombin fragment F 1+2 and oral anticoagulant therapy

This study was undertaken to establish a correlation between prothrombin activation fragment F 1+2 and one-stage prothrombin time (PT) ratios in patients receiving oral anticoagulant therapy. One hundred consecutive patients on warfarin treatment were utilized for this study. The patients had receiv...

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Veröffentlicht in:Thrombosis research 1994-09, Vol.75 (6), p.601-607
Hauptverfasser: Li, Zhuojiang, Wu, Jia, Mammen, Eberhard F.
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description This study was undertaken to establish a correlation between prothrombin activation fragment F 1+2 and one-stage prothrombin time (PT) ratios in patients receiving oral anticoagulant therapy. One hundred consecutive patients on warfarin treatment were utilized for this study. The patients had received warfarin for not less than four days prior to entry into the study. F 1+2 levels and PT ratios were found to be 0.28 ± 0.24 nM/L (mean ± SD) ranging from 0.01 to 1.5 nM/L and 1.62 ± 0.46 (mean ± SD) ranging from 0.97 to 3.11, respectively. Most patients on oral anticoagulants with PT ratios between 1.2 – 1.7 exhibited decreased concentrations of F 1+2. Normal control values of F 1+2 were established for this study in 40 healthy individuals; they were 0.40 ± 0.23 nM/L (median ± SD) ranging from 0.11 to 1.19 nM/L. Mean plasma levels of F 1+2 were significantly lower in the anticoagulated patients as compared to the healthy controls (t = 2.377, p < 0.05). The relationship between F 1+2 levels and PT ratios in the 100 anticoagulated patients was analyzed by linear regression. No significant correlation (r = −0.208) was found between F 1+2 levels and PT ratios. It is concluded that the degree of reduction in F 1+2 levels is not proportional to the intensity of therapy reflected by the PT ratios in anticoagulated patients.
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One hundred consecutive patients on warfarin treatment were utilized for this study. The patients had received warfarin for not less than four days prior to entry into the study. F 1+2 levels and PT ratios were found to be 0.28 ± 0.24 nM/L (mean ± SD) ranging from 0.01 to 1.5 nM/L and 1.62 ± 0.46 (mean ± SD) ranging from 0.97 to 3.11, respectively. Most patients on oral anticoagulants with PT ratios between 1.2 – 1.7 exhibited decreased concentrations of F 1+2. Normal control values of F 1+2 were established for this study in 40 healthy individuals; they were 0.40 ± 0.23 nM/L (median ± SD) ranging from 0.11 to 1.19 nM/L. Mean plasma levels of F 1+2 were significantly lower in the anticoagulated patients as compared to the healthy controls (t = 2.377, p &lt; 0.05). The relationship between F 1+2 levels and PT ratios in the 100 anticoagulated patients was analyzed by linear regression. No significant correlation (r = −0.208) was found between F 1+2 levels and PT ratios. 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Drug treatments ; Prospective Studies ; Prothrombin - analysis ; Prothrombin Fragment F 1+2 ; Prothrombin Time ; prothrombin times ; Vitamin K - antagonists &amp; inhibitors ; Warfarin - administration &amp; dosage ; Warfarin - pharmacology</subject><ispartof>Thrombosis research, 1994-09, Vol.75 (6), p.601-607</ispartof><rights>1994</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-9bbdd89f51bb4bf025040af8d2b84cb22bcc75a33fcc76f5bc79a2065d45ba083</citedby><cites>FETCH-LOGICAL-c386t-9bbdd89f51bb4bf025040af8d2b84cb22bcc75a33fcc76f5bc79a2065d45ba083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0049-3848(94)90172-4$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3421735$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7831679$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Zhuojiang</creatorcontrib><creatorcontrib>Wu, Jia</creatorcontrib><creatorcontrib>Mammen, Eberhard F.</creatorcontrib><title>Prothrombin fragment F 1+2 and oral anticoagulant therapy</title><title>Thrombosis research</title><addtitle>Thromb Res</addtitle><description>This study was undertaken to establish a correlation between prothrombin activation fragment F 1+2 and one-stage prothrombin time (PT) ratios in patients receiving oral anticoagulant therapy. One hundred consecutive patients on warfarin treatment were utilized for this study. The patients had received warfarin for not less than four days prior to entry into the study. F 1+2 levels and PT ratios were found to be 0.28 ± 0.24 nM/L (mean ± SD) ranging from 0.01 to 1.5 nM/L and 1.62 ± 0.46 (mean ± SD) ranging from 0.97 to 3.11, respectively. Most patients on oral anticoagulants with PT ratios between 1.2 – 1.7 exhibited decreased concentrations of F 1+2. Normal control values of F 1+2 were established for this study in 40 healthy individuals; they were 0.40 ± 0.23 nM/L (median ± SD) ranging from 0.11 to 1.19 nM/L. Mean plasma levels of F 1+2 were significantly lower in the anticoagulated patients as compared to the healthy controls (t = 2.377, p &lt; 0.05). The relationship between F 1+2 levels and PT ratios in the 100 anticoagulated patients was analyzed by linear regression. No significant correlation (r = −0.208) was found between F 1+2 levels and PT ratios. 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Drug treatments</subject><subject>Prospective Studies</subject><subject>Prothrombin - analysis</subject><subject>Prothrombin Fragment F 1+2</subject><subject>Prothrombin Time</subject><subject>prothrombin times</subject><subject>Vitamin K - antagonists &amp; inhibitors</subject><subject>Warfarin - administration &amp; dosage</subject><subject>Warfarin - pharmacology</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LAzEQhoMotVb_gcIeRBRZTbLZTXIRpFgVCnrQc0iySRvZj5rsCv33Zu3So6cZmGdmXh4AzhG8QxAV9xASnmaMsGtObjhEFKfkAEwRozzFhOJDMN0jx-AkhC8YIcTzCZhQlqGC8ing777t1r6tlWsS6-WqNk2XLBJ0ixPZlEnrZRWbzulWrvoqdkm3Nl5utqfgyMoqmLOxzsDn4ulj_pIu355f54_LVGes6FKuVFkybnOkFFEW4hwSKC0rsWJEK4yV1jSXWWZjLWyuNOUSwyIvSa4kZNkMXO3ubnz73ZvQidoFbaqYxbR9EJRShIsijyDZgdq3IXhjxca7WvqtQFAMxsSgQww6BCfiz5ggce1ivN-r2pT7pVFRnF-Ocxm0rKKjRruwxzKCEc2G7w87zEQXP854EbQzjTal80Z3omzd_zl-AZ6MhoY</recordid><startdate>19940915</startdate><enddate>19940915</enddate><creator>Li, Zhuojiang</creator><creator>Wu, Jia</creator><creator>Mammen, Eberhard F.</creator><general>Elsevier Ltd</general><general>Elsevier Science</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><scope>7X8</scope></search><sort><creationdate>19940915</creationdate><title>Prothrombin fragment F 1+2 and oral anticoagulant therapy</title><author>Li, Zhuojiang ; Wu, Jia ; Mammen, Eberhard F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-9bbdd89f51bb4bf025040af8d2b84cb22bcc75a33fcc76f5bc79a2065d45ba083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Administration, Oral</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Blood Coagulation Factors - biosynthesis</topic><topic>Blood. Blood coagulation. Reticuloendothelial system</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>oral anticoagulation</topic><topic>Peptide Fragments - analysis</topic><topic>Pharmacology. Drug treatments</topic><topic>Prospective Studies</topic><topic>Prothrombin - analysis</topic><topic>Prothrombin Fragment F 1+2</topic><topic>Prothrombin Time</topic><topic>prothrombin times</topic><topic>Vitamin K - antagonists &amp; inhibitors</topic><topic>Warfarin - administration &amp; dosage</topic><topic>Warfarin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Zhuojiang</creatorcontrib><creatorcontrib>Wu, Jia</creatorcontrib><creatorcontrib>Mammen, Eberhard F.</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><collection>MEDLINE - Academic</collection><jtitle>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Zhuojiang</au><au>Wu, Jia</au><au>Mammen, Eberhard F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prothrombin fragment F 1+2 and oral anticoagulant therapy</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>1994-09-15</date><risdate>1994</risdate><volume>75</volume><issue>6</issue><spage>601</spage><epage>607</epage><pages>601-607</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><coden>THBRAA</coden><abstract>This study was undertaken to establish a correlation between prothrombin activation fragment F 1+2 and one-stage prothrombin time (PT) ratios in patients receiving oral anticoagulant therapy. One hundred consecutive patients on warfarin treatment were utilized for this study. The patients had received warfarin for not less than four days prior to entry into the study. F 1+2 levels and PT ratios were found to be 0.28 ± 0.24 nM/L (mean ± SD) ranging from 0.01 to 1.5 nM/L and 1.62 ± 0.46 (mean ± SD) ranging from 0.97 to 3.11, respectively. Most patients on oral anticoagulants with PT ratios between 1.2 – 1.7 exhibited decreased concentrations of F 1+2. Normal control values of F 1+2 were established for this study in 40 healthy individuals; they were 0.40 ± 0.23 nM/L (median ± SD) ranging from 0.11 to 1.19 nM/L. Mean plasma levels of F 1+2 were significantly lower in the anticoagulated patients as compared to the healthy controls (t = 2.377, p &lt; 0.05). The relationship between F 1+2 levels and PT ratios in the 100 anticoagulated patients was analyzed by linear regression. No significant correlation (r = −0.208) was found between F 1+2 levels and PT ratios. It is concluded that the degree of reduction in F 1+2 levels is not proportional to the intensity of therapy reflected by the PT ratios in anticoagulated patients.</abstract><cop>New York, NY</cop><pub>Elsevier Ltd</pub><pmid>7831679</pmid><doi>10.1016/0049-3848(94)90172-4</doi><tpages>7</tpages></addata></record>
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subjects Administration, Oral
Adult
Aged
Biological and medical sciences
Blood Coagulation Factors - biosynthesis
Blood. Blood coagulation. Reticuloendothelial system
Cohort Studies
Female
Humans
Male
Medical sciences
Middle Aged
oral anticoagulation
Peptide Fragments - analysis
Pharmacology. Drug treatments
Prospective Studies
Prothrombin - analysis
Prothrombin Fragment F 1+2
Prothrombin Time
prothrombin times
Vitamin K - antagonists & inhibitors
Warfarin - administration & dosage
Warfarin - pharmacology
title Prothrombin fragment F 1+2 and oral anticoagulant therapy
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