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 |
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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. |
doi_str_mv | 10.1016/0049-3848(94)90172-4 |
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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 < 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.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/0049-3848(94)90172-4</identifier><identifier>PMID: 7831679</identifier><identifier>CODEN: THBRAA</identifier><language>eng</language><publisher>New York, NY: Elsevier Ltd</publisher><subject>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</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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3421735$$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 < 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.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Blood Coagulation Factors - biosynthesis</subject><subject>Blood. Blood coagulation. Reticuloendothelial system</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>oral anticoagulation</subject><subject>Peptide Fragments - analysis</subject><subject>Pharmacology. 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 & inhibitors</subject><subject>Warfarin - administration & 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 & inhibitors</topic><topic>Warfarin - administration & 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 < 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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