{"id":2681,"date":"2020-06-22T14:43:43","date_gmt":"2020-06-22T18:43:43","guid":{"rendered":"https:\/\/www.med.unc.edu\/wolberglab\/?p=2681"},"modified":"2020-07-27T17:13:26","modified_gmt":"2020-07-27T21:13:26","slug":"the-factor-xiii%e2%80%90a-val34leu-polymorphism-decreases-whole-blood-clot-mass-at-high-fibrinogen-concentrations","status":"publish","type":"post","link":"https:\/\/www.med.unc.edu\/wolberglab\/the-factor-xiii%e2%80%90a-val34leu-polymorphism-decreases-whole-blood-clot-mass-at-high-fibrinogen-concentrations\/","title":{"rendered":"New publication in the Journal of Thrombosis and Haemostasis"},"content":{"rendered":"<h4 class=\"citation__title\"><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/jth.14744\">The factor XIII\u2010A Val34Leu polymorphism decreases whole blood clot mass at high fibrinogen concentrations<\/a><\/h4>\n<div class=\"article-section__content en main\">\n<section id=\"jth14744-sec-0001\" class=\"article-section__content\">\n<h5 id=\"jth14744-sec-0001-title\" class=\"article-section__sub-title section1\"><strong>Background<\/strong>:\u00a0Factor XIII (FXIII) promotes fibrin crosslinking and red blood cell (RBC) retention in clots. The FXIII\u2010A polymorphism, Val34Leu, is associated with protection against venous thrombosis. This effect is hypothesized to result from fibrinogen concentration\u2010dependent changes in fibrin structure. Effects of the FXIII\u2010A Val34Leu polymorphism in whole blood clots have not been investigated. <strong>Aim<\/strong>: Characterize effects of FXIII\u2010A Val34Leu polymorphism and fibrinogen on whole blood clots. <strong>Methods<\/strong>: We isolated platelet\u2010poor plasmas from human donors (FXIII<sup>Val\/Val<\/sup>, FXIII<sup>Val\/Leu<\/sup>, FXIII<sup>Leu\/Leu<\/sup>), reconstituted plasmas with platelets and RBCs, and triggered clotting. We assessed contributions of gender, age, clotting times, thrombin generation, FXIII activity, FXIII\u2010A Val34Leu polymorphism, and fibrinogen to clot mass. We also reconstituted FXIII\u2010depleted plasma with platelets, RBCs, and purified FXIII<sup>Val\/Val<\/sup> or FXIII<sup>Leu\/Leu<\/sup>, varied fibrinogen, and characterized effects on clot mass. <strong>Results<\/strong>: Clot mass was associated with age, fibrinogen, prothrombin time, and thrombin generation. Clots reconstituted with plasmas from individuals with FXIII\u2010A<sup>Val\/Val<\/sup> and FXIII\u2010A<sup>Val\/Leu<\/sup> did not differ in mass from clots with FXIII\u2010A<sup>Leu\/Leu<\/sup>. However, clots containing a 34Val allele demonstrated a fibrinogen concentration\u2010dependent increase in mass, whereas clots with homozygous 34Leu did not. In plasmas with high fibrinogen, mass was higher for clots with 34Val alleles compared with clots with homozygous 34Leu. In clots reconstituted with purified FXIII, increasing fibrinogen enhanced clot mass in the presence of 34Val, but decreased mass in the presence of 34Leu. <strong>Conclusions<\/strong>: FXIII 34Leu mitigates the effect of elevated fibrinogen on whole blood clot mass. The Val34Leu polymorphism may protect against venous thrombosis by reducing clot mass.<\/h5>\n<\/section>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>The factor XIII\u2010A Val34Leu polymorphism decreases whole blood clot mass at high fibrinogen concentrations Background:\u00a0Factor XIII (FXIII) promotes fibrin crosslinking and red blood cell (RBC) retention in clots. The FXIII\u2010A polymorphism, Val34Leu, is associated with protection against venous thrombosis. This effect is hypothesized to result from fibrinogen concentration\u2010dependent changes in fibrin structure. Effects of the &hellip; <a href=\"https:\/\/www.med.unc.edu\/wolberglab\/the-factor-xiii%e2%80%90a-val34leu-polymorphism-decreases-whole-blood-clot-mass-at-high-fibrinogen-concentrations\/\" aria-label=\"Read more about New publication in the Journal of Thrombosis and Haemostasis\">Read more<\/a><\/p>\n","protected":false},"author":15383,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":"","_links_to":"","_links_to_target":""},"categories":[2],"tags":[],"class_list":["post-2681","post","type-post","status-publish","format-standard","hentry","category-news","odd"],"acf":[],"featured_image":false,"featured_image_medium":false,"featured_image_medium_large":false,"featured_image_large":false,"featured_image_thumbnail":false,"featured_image_alt":false,"category_details":[{"name":"News","link":"https:\/\/www.med.unc.edu\/wolberglab\/category\/news\/"}],"tag_details":[],"_links_to":[],"_links_to_target":[],"_links":{"self":[{"href":"https:\/\/www.med.unc.edu\/wolberglab\/wp-json\/wp\/v2\/posts\/2681","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.med.unc.edu\/wolberglab\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.med.unc.edu\/wolberglab\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.med.unc.edu\/wolberglab\/wp-json\/wp\/v2\/users\/15383"}],"replies":[{"embeddable":true,"href":"https:\/\/www.med.unc.edu\/wolberglab\/wp-json\/wp\/v2\/comments?post=2681"}],"version-history":[{"count":0,"href":"https:\/\/www.med.unc.edu\/wolberglab\/wp-json\/wp\/v2\/posts\/2681\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.med.unc.edu\/wolberglab\/wp-json\/wp\/v2\/media?parent=2681"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.med.unc.edu\/wolberglab\/wp-json\/wp\/v2\/categories?post=2681"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.med.unc.edu\/wolberglab\/wp-json\/wp\/v2\/tags?post=2681"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}