Swanepoel, A.C. (Albe Carina)Visagie, AmcoisDe Lange, ZeldaEmmerson, OdetteNielsen, Vance G.Pretorius, Etheresia2016-12-052016-10Swanepoel, AC, Visagie, A, De Lange, Z, Emmerson, O, Nielsen, VG & Pretorius, E 2016, 'The clinical relevance of altered fibrinogen packaging in the presence of 17β-estradiol and progesterone', Thrombosis Research, vol. 146, pp. 23-34.0049-384810.1016/j.thromres.2016.08.022http://hdl.handle.net/2263/58348BACKGROUND : The effect of endogenous hormone concentrations, specifically 17β-estradiol and progesterone, on fibrin network formation has not been established. OBJECTIVES : It is essential to understand natural hormone mechanisms since these hormones are still present in circulation while hormonal contraceptives, which are associated with increased risk of venous thromboembolism, are used. METHODS : Due to the fact that these hormones are known to increase hypercoagulability and the prothrombotic state scanning electron microscopy (SEM), atomic force microscopy (AFM), thromboelastography (TEG) and turbidimetry were employed to investigate the morphology, surface roughness, viscoelastic properties and formation and lysis of fibrin. RESULTS : 17β-estradiol and progesterone showed hypercoagulable viscoelastic properties and decreased the diameter and surface roughness of fibrin while increasing dense matted deposit occurrence. Our results suggest that the additional burden of hormonal load, together with the presence of endogenous estrogen and progesterone, may result in a prothrombotic and hypercoagulable state in females with an inflammatory predisposition. CONCLUSION : Our results are of clinical importance when considering hormones as either pathological agent or therapeutic intervention as will be assessed in future investigation.en© 2016 Elsevier Ltd. All rights reserved. Notice : this is the author’s version of a work that was accepted for publication in Thrombosis Research . Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. A definitive version was subsequently published in Thrombosis Research, vol. 146, pp. 23-34, 2016. doi : 10.1016/j.thromres.2016.08.022.17β-estradiolFibrinogenFibrinProgesteroneThrombophiliaCirculationHormonal contraceptivesVenous thromboembolismNatural hormoneState scanning electron microscopy (SEM)Atomic force microscopy (AFM)Thromboelastography (TEG)TurbidimetryPostprint Article