Enhanced lysis and accelerated establishment of viscoelastic properties of fibrin clots are associated with pulmonary embolism
The factors that contribute to pulmonary embolism (PE), a potentially fatal complication of deep vein thrombosis (DVT), remain poorly understood. Whereas fibrin clot structure and functional properties have been implicated in the pathology of venous thromboembolism and the risk for cardiovascular co...
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Published in | American journal of physiology. Lung cellular and molecular physiology Vol. 306; no. 5; pp. L397 - L404 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Physiological Society
01.03.2014
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Series | Translational Research in Acute Lung Injury and Pulmonary Fibrosis |
Subjects | |
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Abstract | The factors that contribute to pulmonary embolism (PE), a potentially fatal complication of deep vein thrombosis (DVT), remain poorly understood. Whereas fibrin clot structure and functional properties have been implicated in the pathology of venous thromboembolism and the risk for cardiovascular complications, their significance in PE remains uncertain. Therefore, we systematically compared and quantified clot formation and lysis time, plasminogen levels, viscoelastic properties, activated factor XIII cross-linking, and fibrin clot structure in isolated DVT and PE subjects. Clots made from plasma of PE subjects showed faster clot lysis times with no differences in lag time, rate of clot formation, or maximum absorbance of turbidity compared with DVT. Differences in lysis times were not due to alterations in plasminogen levels. Compared with DVT, clots derived from PE subjects showed accelerated establishment of viscoelastic properties, documented by a decrease in lag time and an increase in the rate of viscoelastic property formation. The rate and extent of fibrin cross-linking by activated factor XIII were similar between clots from DVT and PE subjects. Electron microscopy revealed that plasma fibrin clots from PE subjects exhibited lower fiber density compared with those from DVT subjects. These data suggest that clot structure and functional properties differ between DVT and PE subjects and provide insights into mechanisms that may regulate embolization. |
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AbstractList | The factors that contribute to pulmonary embolism (PE), a potentially fatal complication of deep vein thrombosis (DVT), remain poorly understood. Whereas fibrin clot structure and functional properties have been implicated in the pathology of venous thromboembolism and the risk for cardiovascular complications, their significance in PE remains uncertain. Therefore, we systematically compared and quantified clot formation and lysis time, plasminogen levels, viscoelastic properties, activated factor XIII cross-linking, and fibrin clot structure in isolated DVT and PE subjects. Clots made from plasma of PE subjects showed faster clot lysis times with no differences in lag time, rate of clot formation, or maximum absorbance of turbidity compared with DVT. Differences in lysis times were not due to alterations in plasminogen levels. Compared with DVT, clots derived from PE subjects showed accelerated establishment of viscoelastic properties, documented by a decrease in lag time and an increase in the rate of viscoelastic property formation. The rate and extent of fibrin cross-linking by activated factor XIII were similar between clots from DVT and PE subjects. Electron microscopy revealed that plasma fibrin clots from PE subjects exhibited lower fiber density compared with those from DVT subjects. These data suggest that clot structure and functional properties differ between DVT and PE subjects and provide insights into mechanisms that may regulate embolization.The factors that contribute to pulmonary embolism (PE), a potentially fatal complication of deep vein thrombosis (DVT), remain poorly understood. Whereas fibrin clot structure and functional properties have been implicated in the pathology of venous thromboembolism and the risk for cardiovascular complications, their significance in PE remains uncertain. Therefore, we systematically compared and quantified clot formation and lysis time, plasminogen levels, viscoelastic properties, activated factor XIII cross-linking, and fibrin clot structure in isolated DVT and PE subjects. Clots made from plasma of PE subjects showed faster clot lysis times with no differences in lag time, rate of clot formation, or maximum absorbance of turbidity compared with DVT. Differences in lysis times were not due to alterations in plasminogen levels. Compared with DVT, clots derived from PE subjects showed accelerated establishment of viscoelastic properties, documented by a decrease in lag time and an increase in the rate of viscoelastic property formation. The rate and extent of fibrin cross-linking by activated factor XIII were similar between clots from DVT and PE subjects. Electron microscopy revealed that plasma fibrin clots from PE subjects exhibited lower fiber density compared with those from DVT subjects. These data suggest that clot structure and functional properties differ between DVT and PE subjects and provide insights into mechanisms that may regulate embolization. The factors that contribute to pulmonary embolism (PE), a potentially fatal complication of deep vein thrombosis (DVT), remain poorly understood. Whereas fibrin clot structure and functional properties have been implicated in the pathology of venous thromboembolism and the risk for cardiovascular complications, their significance in PE remains uncertain. Therefore, we systematically compared and quantified clot formation and lysis time, plasminogen levels, viscoelastic properties, activated factor XIII cross-linking, and fibrin clot structure in isolated DVT and PE subjects. Clots made from plasma of PE subjects showed faster clot lysis times with no differences in lag time, rate of clot formation, or maximum absorbance of turbidity compared with DVT. Differences in lysis times were not due to alterations in plasminogen levels. Compared with DVT, clots derived from PE subjects showed accelerated establishment of viscoelastic properties, documented by a decrease in lag time and an increase in the rate of viscoelastic property formation. The rate and extent of fibrin cross-linking by activated factor XIII were similar between clots from DVT and PE subjects. Electron microscopy revealed that plasma fibrin clots from PE subjects exhibited lower fiber density compared with those from DVT subjects. These data suggest that clot structure and functional properties differ between DVT and PE subjects and provide insights into mechanisms that may regulate embolization. The factors that contribute to pulmonary embolism (PE), a potentially fatal complication of deep vein thrombosis (DVT), remain poorly understood. Whereas fibrin clot structure and functional properties have been implicated in the pathology of venous thromboembolism and the risk for cardiovascular complications, their significance in PE remains uncertain. Therefore, we systematically compared and quantified clot formation and lysis time, plasminogen levels, viscoelastic properties, activated factor XIII cross-linking, and fibrin clot structure in isolated DVT and PE subjects. Clots made from plasma of PE subjects showed faster clot lysis times with no differences in lag time, rate of clot formation, or maximum absorbance of turbidity compared with DVT. Differences in lysis times were not due to alterations in plasminogen levels. Compared with DVT, clots derived from PE subjects showed accelerated establishment of viscoelastic properties, documented by a decrease in lag time and an increase in the rate of viscoelastic property formation. The rate and extent of fibrin cross-linking by activated factor XIII were similar between clots from DVT and PE subjects. Electron microscopy revealed that plasma fibrin clots from PE subjects exhibited lower fiber density compared with those from DVT subjects. These data suggest that clot structure and functional properties differ between DVT and PE subjects and provide insights into mechanisms that may regulate embolization. [PUBLICATION ABSTRACT] |
Author | Lightfoot, Richard T. Chernysh, Irina N. Cuker, Adam Nagaswami, Chandrasekaran Martinez, Marissa R. Weisel, John W. Crichlow, Amanda Ischiropoulos, Harry Mills, Angela M. |
Author_xml | – sequence: 1 givenname: Marissa R. surname: Martinez fullname: Martinez, Marissa R. organization: Departments of Pediatrics and Pharmacology, Children's Hospital of Philadelphia and the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania – sequence: 2 givenname: Adam surname: Cuker fullname: Cuker, Adam organization: Department of Medicine, the Raymond and Ruth Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania – sequence: 3 givenname: Angela M. surname: Mills fullname: Mills, Angela M. organization: Department of Emergency Medicine, the Raymond and Ruth Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; and – sequence: 4 givenname: Amanda surname: Crichlow fullname: Crichlow, Amanda organization: Department of Emergency Medicine, the Raymond and Ruth Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; and – sequence: 5 givenname: Richard T. surname: Lightfoot fullname: Lightfoot, Richard T. organization: Departments of Pediatrics and Pharmacology, Children's Hospital of Philadelphia and the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania – sequence: 6 givenname: Irina N. surname: Chernysh fullname: Chernysh, Irina N. organization: Department of Cell and Developmental Biology, the Raymond and Ruth Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania – sequence: 7 givenname: Chandrasekaran surname: Nagaswami fullname: Nagaswami, Chandrasekaran organization: Department of Cell and Developmental Biology, the Raymond and Ruth Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania – sequence: 8 givenname: John W. surname: Weisel fullname: Weisel, John W. organization: Department of Cell and Developmental Biology, the Raymond and Ruth Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania – sequence: 9 givenname: Harry surname: Ischiropoulos fullname: Ischiropoulos, Harry organization: Departments of Pediatrics and Pharmacology, Children's Hospital of Philadelphia and the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania |
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Snippet | The factors that contribute to pulmonary embolism (PE), a potentially fatal complication of deep vein thrombosis (DVT), remain poorly understood. Whereas... |
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SubjectTerms | Adult Aged Blood clots Blood Coagulation - physiology Call for Papers Cross-Linking Reagents - metabolism Elasticity Embolisms Factor XIIIa - metabolism Female Fibrin - chemistry Fibrin - metabolism Fibrin - ultrastructure Fibrinogen - metabolism Fibrinolysis - physiology Health risks Humans Male Microscopy, Electron, Scanning Middle Aged Plasminogen - metabolism Prospective Studies Pulmonary arteries Pulmonary Embolism - etiology Pulmonary Embolism - metabolism Thromboembolism Turbidity Venous Thrombosis - complications Viscoelasticity |
Title | Enhanced lysis and accelerated establishment of viscoelastic properties of fibrin clots are associated with pulmonary embolism |
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