4.7 Article

Fibrin-Targeted Magnetic Resonance Imaging Allows In Vivo Quantification of Thrombus Fibrin Content and Identifies Thrombi Amenable for Thrombolysis

Journal

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Volume 34, Issue 6, Pages 1193-1198

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/ATVBAHA.113.302931

Keywords

fibrin; magnetic resonance imaging; molecular imaging; thrombolytic therapy; venous thrombosis

Funding

  1. British Heart Foundation Centre of Excellence at King's College London
  2. Wellcome Trust
  3. Engineering and Physical Sciences Research Council Medical Engineering Centre at King's College London [WT 088641/Z/09/Z]
  4. National Institute for Health Research Biomedical Research Centre of Guy's and St Thomas' Trust
  5. King's College London
  6. Chilean Agency for Research in Science and Technology [FONDECYT 1130379]
  7. Wellcome Trust Clinical Research Training Fellowship [WT 090252/Z/09/Z]
  8. British Heart Foundation [FS/11/37/28819, RG/12/1/29262] Funding Source: researchfish
  9. National Institute for Health Research [CL-2011-17-006] Funding Source: researchfish
  10. Wellcome Trust [090252/Z/09/Z] Funding Source: Wellcome Trust

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Objective Deep venous thrombosis is a major health problem. Thrombolytic therapies are effective in recanalizing the veins and preventing post-thrombotic complications, but there is no consensus on selection criteria. The aim of this study was to investigate a fibrin-specific MRI contrast agent (EP-2104R) for the accurate quantification of thrombus' fibrin content in vivo and for the identification of thrombus suitable for thrombolysis. Approach and Results Venous thrombosis was induced in the inferior vena cava of 8- to 10-week-old male BALB/C mice and MRI performed 2, 4, 7, 10, 14, and 21 days later. Eighteen mice were scanned at each time point pre and 2 hours post injection of EP-2104R (8.0 mol/kg) with 12 mice at each time point used to correlate fibrin contrast uptake with thrombus' histological stage and fibrin content. Six mice at each time point were immediately subjected to intravascular thrombolytic therapy (10 mg/kg of tissue-type plasminogen activator). Mice were imaged to assess response to lytic therapy 24 hours after thrombolytic treatment. Two mice at each time point were scanned post injection of 0.2 mmol/kg of Gd-DTPA (gadolinium with diethylenetriaminepentacetate, Magnevist, Schering AG, Berlin, Germany) for control purpose. Contrast uptake was correlated positively with the fibrin content of the thrombus measured by Western blotting (R-2=0.889; P<0.001). Thrombus relaxation rate (R-1) post contrast and the change in visualized thrombus size on late gadolinium enhancement inversion recovery MRI pre-EP-2104R and post-EP-2104R injection were the best predictors for successful thrombolysis (area under the curve, 0.989 [95% confidence interval, 0.97-1.00] and 0.994 [95% confidence interval, 0.98-1.00] respectively). Conclusions MRI with a fibrin-specific contrast agent accurately estimates thrombus fibrin content in vivo and identifies thrombi that are amenable for thrombolysis.

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