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Submitted on March 22, 2002
From the Academic Unit of Molecular Vascular Medicine,
University of Leeds, United
Kingdom. * To whom correspondence should be addressed. E-mail: r.a.s.ariens{at}leeds.ac.uk.
BackgroundA family history of premature coronary artery disease (CAD) is an independent cardiovascular risk factor. Fibrin clots composed of dense fiber networks are found in young CAD patients and may occur in the relatives of such individuals. Methods and ResultsThe ex vivo fibrin structure of 100 healthy male relatives of patients with premature CAD and 100 age-matched control subjects was assessed by measurement of permeability (Ks), fiber mass-length ratio (µ), and turbidity (lag phase and maximum absorbency [max ConclusionsThe male relatives of patients with premature CAD form fibrin clots that begin polymerization more quickly, have thicker fibers, and are less permeable than those of control subjects.
Revised on July 26, 2002
Accepted on July 26, 2002
Altered Fibrin Clot Structure in the Healthy
Relatives of Patients With Premature Coronary Artery
Disease
Joseph D. Mills MRCP,
Abs]). Scanning electron microscopy was performed on selected samples. Relatives and controls shared similar levels of conventional cardiovascular risk factors. Ks was lower in relatives than in controls, 12.2 (11.1 to 13.3) versus 15.2 (14.0 to 16.5) x10-9 cm2 ( P<0.001), associated with a smaller decrease in µ, 8.5 (7.7 to 9.2) versus 9.7 (8.9 to 10.5) x1013 Da/cm (P<0.05), respectively. Lag phase was shorter in relatives than in controls, 39 (37 to 41) versus 47 (44 to 50) seconds (P<0.001), and max
Abs was higher in relatives, 0.78 (0.74 to 0.82) versus 0.71 (0.67 to 0.74) in controls (P=0.02), which indicates the presence of thicker fibers in relatives. After adjustment for fibrinogen levels, lag phase and Ks remained significantly different between relatives and control subjects. Scanning electron microscopy images confirmed increased fiber diameter in relatives, possibly of reduced density. Factor XIII Val34Leu and fibrinogen A
Thr312Ala and Bß -455 G/A showed no association with clot structure.
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