Coronary thrombosis is an important determinant of prognosis in patients wi
th acute coronary syndromes (ACS). However, the identification of patients
at high-risk for progression of coronary thrombosis is difficult in part be
cause we currently lack clinically meaningful laboratory methods for its de
tection. The most pron-dsing approaches involve the measurement in plasma o
f markers of fibrin formation and degradation. Thrombin activity, as reflec
ted by plasma or urine concentrations of fibrinopeptide A, is increased in
patients with ACS and is associated with adverse outcome. However, the use
of fibrinopeptide A as a marker of fibrin formation is limited by the very
short half-life of the compound, by artifact due to sample aquisition, and
by extremely long turnaround times. To overcome these limitations, measurem
ent of soluble fibrin has been proposed. We have recently explored the prog
nostic value of a new fibrin-specific ELISA assay for soluble fibrin in pat
ients with ACS and found that patients with highest levels had a twofold in
creased risk of early and late cardiac events. Increases in plasma concentr
ations of cross-linked fibrin degradation products (XL-FDPs), which reflect
increased fibrin turn-over, are a marker of risk for complications of myoc
ardial infarction. However, until recently, assays for XL-FDPs lacked speci
ficity, because they did not distinguish between fibrin and fibrinogen degr
adation products. Recently, fibrin-specific ELISAs have been described and
a rapid whole blood assay for D-dimer has been developed. We recently valid
ated the prognostic value of this whole blood agglutination assay in patien
ts with ACS.
The results suggest that: (1) the detection of significant activation of th
e coagulation and/or fibrinolytic system may be important for rapid risk st
ratification of patients with ACS; (2) patients with biochemical evidence o
f ongoing coronary thrombosis may particularly benefit from aggressive anti
thrombotic strategies; (3) sequential measurements of these markers may be
useful to guide antithrombotic treatment during the unstable phase of coron
ary artery disease. (C) 2001 Elsevier Science BN. All rights reserved.