CVD risk factors are related to plasma fibrin clot properties independent of total and or γ’ fibrinogen concentration

Abstract Introduction Cardiovascular disease (CVD) risk factors are associated with total fibrinogen concentration and/or altered clot structure. It is however, unclear whether such associations with clot structure are ascribed to fibrinogen concentration or other independent mechanisms. We aimed to...

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Veröffentlicht in:Thrombosis research 2014-11, Vol.134 (5), p.963-969
Hauptverfasser: Kotzé, Retha C.M, Ariëns, Robert A.S, de Lange, Zelda, Pieters, Marlien
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container_issue 5
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creator Kotzé, Retha C.M
Ariëns, Robert A.S
de Lange, Zelda
Pieters, Marlien
description Abstract Introduction Cardiovascular disease (CVD) risk factors are associated with total fibrinogen concentration and/or altered clot structure. It is however, unclear whether such associations with clot structure are ascribed to fibrinogen concentration or other independent mechanisms. We aimed to determine whether CVD risk factors associated with increased total and/or γ’ fibrinogen concentration, were also associated with altered fibrin clot properties and secondly whether such associations were due to the fibrinogen concentration or through independent associations. Materials and methods In a plasma setting CVD risk factors (including total and γ’ fibrinogen concentration) were cross-sectionally analysed in 2010 apparently healthy black South African participants. Kinetics of clot formation (lag time, slope and maximum absorbance) as well as clot lysis times were calculated from turbidity curves. Results Of the measured CVD risk factors age, metabolic syndrome, C-reactive protein (CRP), high density lipoprotein (HDL)-cholesterol and homocysteine were significantly associated with altered fibrin clot properties after adjustment for total and or γ’ fibrinogen concentration. Aging was associated with thicker fibres (p = 0.004) while both metabolic syndrome and low HDL-cholesterol levels were associated with lower rates of lateral aggregation (slope), (p = 0.0004 and p = 0.0009), and the formation of thinner fibres (p = 0.007 and p = 0.0004). Elevated CRP was associated with increased rates of lateral aggregation (p = 0.002) and consequently thicker fibres (p < 0.0001). Hyperhomocysteinemia was associated with increased rates of lateral aggregation (p = 0.0007) without affecting fibre thickness. Conclusion Final clot structure may contribute to increased CVD risk in vivo through associations with other CVD risk factors independent from total or γ’ fibrinogen concentration.
doi_str_mv 10.1016/j.thromres.2014.08.018
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It is however, unclear whether such associations with clot structure are ascribed to fibrinogen concentration or other independent mechanisms. We aimed to determine whether CVD risk factors associated with increased total and/or γ’ fibrinogen concentration, were also associated with altered fibrin clot properties and secondly whether such associations were due to the fibrinogen concentration or through independent associations. Materials and methods In a plasma setting CVD risk factors (including total and γ’ fibrinogen concentration) were cross-sectionally analysed in 2010 apparently healthy black South African participants. Kinetics of clot formation (lag time, slope and maximum absorbance) as well as clot lysis times were calculated from turbidity curves. Results Of the measured CVD risk factors age, metabolic syndrome, C-reactive protein (CRP), high density lipoprotein (HDL)-cholesterol and homocysteine were significantly associated with altered fibrin clot properties after adjustment for total and or γ’ fibrinogen concentration. Aging was associated with thicker fibres (p = 0.004) while both metabolic syndrome and low HDL-cholesterol levels were associated with lower rates of lateral aggregation (slope), (p = 0.0004 and p = 0.0009), and the formation of thinner fibres (p = 0.007 and p = 0.0004). Elevated CRP was associated with increased rates of lateral aggregation (p = 0.002) and consequently thicker fibres (p &lt; 0.0001). Hyperhomocysteinemia was associated with increased rates of lateral aggregation (p = 0.0007) without affecting fibre thickness. Conclusion Final clot structure may contribute to increased CVD risk in vivo through associations with other CVD risk factors independent from total or γ’ fibrinogen concentration.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/j.thromres.2014.08.018</identifier><identifier>PMID: 25213709</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Adult ; Blood Coagulation ; Cardiovascular Diseases - blood ; Cardiovascular Diseases - etiology ; Cardiovascular Diseases - metabolism ; CVD risk factors ; Female ; Fibrin - analysis ; Fibrin - metabolism ; Fibrin Clot Lysis Time ; Fibrin clot structure ; Fibrinogen ; Fibrinogens, Abnormal - analysis ; Fibrinolysis ; Hematology, Oncology and Palliative Medicine ; Humans ; Male ; Middle Aged ; Plasma ; Risk Factors</subject><ispartof>Thrombosis research, 2014-11, Vol.134 (5), p.963-969</ispartof><rights>Elsevier Ltd</rights><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. 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It is however, unclear whether such associations with clot structure are ascribed to fibrinogen concentration or other independent mechanisms. We aimed to determine whether CVD risk factors associated with increased total and/or γ’ fibrinogen concentration, were also associated with altered fibrin clot properties and secondly whether such associations were due to the fibrinogen concentration or through independent associations. Materials and methods In a plasma setting CVD risk factors (including total and γ’ fibrinogen concentration) were cross-sectionally analysed in 2010 apparently healthy black South African participants. Kinetics of clot formation (lag time, slope and maximum absorbance) as well as clot lysis times were calculated from turbidity curves. Results Of the measured CVD risk factors age, metabolic syndrome, C-reactive protein (CRP), high density lipoprotein (HDL)-cholesterol and homocysteine were significantly associated with altered fibrin clot properties after adjustment for total and or γ’ fibrinogen concentration. Aging was associated with thicker fibres (p = 0.004) while both metabolic syndrome and low HDL-cholesterol levels were associated with lower rates of lateral aggregation (slope), (p = 0.0004 and p = 0.0009), and the formation of thinner fibres (p = 0.007 and p = 0.0004). Elevated CRP was associated with increased rates of lateral aggregation (p = 0.002) and consequently thicker fibres (p &lt; 0.0001). Hyperhomocysteinemia was associated with increased rates of lateral aggregation (p = 0.0007) without affecting fibre thickness. Conclusion Final clot structure may contribute to increased CVD risk in vivo through associations with other CVD risk factors independent from total or γ’ fibrinogen concentration.</description><subject>Adult</subject><subject>Blood Coagulation</subject><subject>Cardiovascular Diseases - blood</subject><subject>Cardiovascular Diseases - etiology</subject><subject>Cardiovascular Diseases - metabolism</subject><subject>CVD risk factors</subject><subject>Female</subject><subject>Fibrin - analysis</subject><subject>Fibrin - metabolism</subject><subject>Fibrin Clot Lysis Time</subject><subject>Fibrin clot structure</subject><subject>Fibrinogen</subject><subject>Fibrinogens, Abnormal - analysis</subject><subject>Fibrinolysis</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Plasma</subject><subject>Risk Factors</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTuOFDEQhi0EYoeFK6wckkzjZ7udINDwlFYi4CEyy2OXwbPd7cb2IDbjGpyDe3AIToJHM0tAQmI7-P6q8lcIXVDSUUL7R7uufs5pylA6RqjoyNAROtxCKzoovWZCsdtoRYjQaz6I4QzdK2VHCFVUy7vojElGuSJ6hb5tPjzDOZYrHKyrKRdsM-AMo63gcU14GW2ZLA5xm-OM3ZgqXnJaINcIBcfZwwLtmCtOofHVjtjOHqeMf_38_f3HKZg-QQun2TUw2xrTfB_dCXYs8OB0n6P3L56_27xaX755-Xrz9HLtBON1Lfkg_VZSLXrKpJTWOek54UqqoITqBxUCD8Tq0DsW-NYK76D3XmlQjinCz9HDY9029Zc9lGqmWByMo50h7YuhPdO614PuG9ofUZdTKRmCWXKcbL42lJiDdbMzN9bNwbohg2nWW_Di1GO_ncD_jd1obsCTIwDtp18jZFNchGbDxwyuGp_i_3s8_qeEG-McnR2v4BrKLu3z3DwaagozxLw97P6weiraS4qP_A9o-K91</recordid><startdate>20141101</startdate><enddate>20141101</enddate><creator>Kotzé, Retha C.M</creator><creator>Ariëns, Robert A.S</creator><creator>de Lange, Zelda</creator><creator>Pieters, Marlien</creator><general>Elsevier Ltd</general><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>20141101</creationdate><title>CVD risk factors are related to plasma fibrin clot properties independent of total and or γ’ fibrinogen concentration</title><author>Kotzé, Retha C.M ; Ariëns, Robert A.S ; de Lange, Zelda ; Pieters, Marlien</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-5385db5194612555acc5d303757f747687ff3f0a9f6c2f3ba4dce6dd79e7c2703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Blood Coagulation</topic><topic>Cardiovascular Diseases - blood</topic><topic>Cardiovascular Diseases - etiology</topic><topic>Cardiovascular Diseases - metabolism</topic><topic>CVD risk factors</topic><topic>Female</topic><topic>Fibrin - analysis</topic><topic>Fibrin - metabolism</topic><topic>Fibrin Clot Lysis Time</topic><topic>Fibrin clot structure</topic><topic>Fibrinogen</topic><topic>Fibrinogens, Abnormal - analysis</topic><topic>Fibrinolysis</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Plasma</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kotzé, Retha C.M</creatorcontrib><creatorcontrib>Ariëns, Robert A.S</creatorcontrib><creatorcontrib>de Lange, Zelda</creatorcontrib><creatorcontrib>Pieters, Marlien</creatorcontrib><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>Kotzé, Retha C.M</au><au>Ariëns, Robert A.S</au><au>de Lange, Zelda</au><au>Pieters, Marlien</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CVD risk factors are related to plasma fibrin clot properties independent of total and or γ’ fibrinogen concentration</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>2014-11-01</date><risdate>2014</risdate><volume>134</volume><issue>5</issue><spage>963</spage><epage>969</epage><pages>963-969</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><abstract>Abstract Introduction Cardiovascular disease (CVD) risk factors are associated with total fibrinogen concentration and/or altered clot structure. It is however, unclear whether such associations with clot structure are ascribed to fibrinogen concentration or other independent mechanisms. We aimed to determine whether CVD risk factors associated with increased total and/or γ’ fibrinogen concentration, were also associated with altered fibrin clot properties and secondly whether such associations were due to the fibrinogen concentration or through independent associations. Materials and methods In a plasma setting CVD risk factors (including total and γ’ fibrinogen concentration) were cross-sectionally analysed in 2010 apparently healthy black South African participants. Kinetics of clot formation (lag time, slope and maximum absorbance) as well as clot lysis times were calculated from turbidity curves. Results Of the measured CVD risk factors age, metabolic syndrome, C-reactive protein (CRP), high density lipoprotein (HDL)-cholesterol and homocysteine were significantly associated with altered fibrin clot properties after adjustment for total and or γ’ fibrinogen concentration. Aging was associated with thicker fibres (p = 0.004) while both metabolic syndrome and low HDL-cholesterol levels were associated with lower rates of lateral aggregation (slope), (p = 0.0004 and p = 0.0009), and the formation of thinner fibres (p = 0.007 and p = 0.0004). Elevated CRP was associated with increased rates of lateral aggregation (p = 0.002) and consequently thicker fibres (p &lt; 0.0001). Hyperhomocysteinemia was associated with increased rates of lateral aggregation (p = 0.0007) without affecting fibre thickness. Conclusion Final clot structure may contribute to increased CVD risk in vivo through associations with other CVD risk factors independent from total or γ’ fibrinogen concentration.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>25213709</pmid><doi>10.1016/j.thromres.2014.08.018</doi><tpages>7</tpages></addata></record>
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subjects Adult
Blood Coagulation
Cardiovascular Diseases - blood
Cardiovascular Diseases - etiology
Cardiovascular Diseases - metabolism
CVD risk factors
Female
Fibrin - analysis
Fibrin - metabolism
Fibrin Clot Lysis Time
Fibrin clot structure
Fibrinogen
Fibrinogens, Abnormal - analysis
Fibrinolysis
Hematology, Oncology and Palliative Medicine
Humans
Male
Middle Aged
Plasma
Risk Factors
title CVD risk factors are related to plasma fibrin clot properties independent of total and or γ’ fibrinogen concentration
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