Published online before print April 21, 2003, doi: 10.1161/01.CIR.0000066690.89407.CE
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(Circulation. 2003;107:2326.)
© 2003 American Heart Association, Inc.
Clinical Investigation and Reports |
Functional Analysis of the Fibrinogen A
Thr312Ala Polymorphism
Effects on Fibrin Structure and Function
From the Academic Unit of Molecular Vascular Medicine (K.F.S., P.J.G., A.M.C., R.A.S.A.), Research School of Medicine, University of Leeds, Leeds General Infirmary, Leeds, UK, and Department of Cell and Developmental Biology (T.S., J.W.W.), University of Pennsylvania School of Medicine, Philadelphia, Pa.
Correspondence to Peter J. Grant, MD, FRCP, Academic Unit of Molecular Vascular Medicine, Research School of Medicine, G Floor, Martin Wing, Leeds General Infirmary, Leeds LS1 3EX, UK. E-mail P.J.Grant{at}leeds.ac.uk
Background— The fibrinogen A
Thr312Ala polymorphism occurs within the C domain of fibrinogen, which is important for lateral aggregation and factor XIII-induced cross-linking of fibrin fibers. We have previously shown an association of Ala312 fibrinogen with poststroke mortality in subjects with atrial fibrillation and with pulmonary embolism in subjects with venous thrombosis.
Methods and Results— We studied the properties of clots formed from purified Ala312 and Thr312 fibrinogen and found that Ala312 fibrinogen produces stiffer clots, associated with increased chain cross-linking, as demonstrated by SDS-Page. On electron microscopy analysis, we found larger fiber diameters in the Ala312 clots and observed a lower number of fibers per square micrometer. The number of branch points per square micrometer was similar between genotypes.
Conclusions— Our study shows that Ala312 influences clot structure and properties by increased factor XIII cross-linking and formation of thicker fibrin fibers. These findings may provide a mechanism by which Ala312 fibrinogen could predispose to clot embolization.
Key Words: fibrinogen • fibrin • thrombosis
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