TY - JOUR
T1 - Physiological predictors of acute coronary syndromes
T2 - emerging insights from the plaque to the vulnerable patient
AU - Ford, Thomas J.
AU - Berry, Colin
AU - De Bruyne, Bernard
AU - Yong, Andy S. C.
AU - Barlis, Peter
AU - Fearon, William F.
AU - Ng, Martin K. C.
PY - 2017/12/26
Y1 - 2017/12/26
N2 - In this review, the authors explore the evolving evidence linking physiological assessment of coronary artery disease with plaque progression and vulnerability. Reducing adverse clinical events remains the ultimate goal for diagnostic tests, and this review highlights evidence supporting the prognostic value of physiological metrics in predicting outcomes. Historical and contemporary studies support synergy among lesion severity, ischemia, plaque vulnerability, and patient prognosis. Ischemia contributes to clinical events through association with plaque burden, but this review addresses the emerging concept that it associates with atherothrombosis via disturbed lesion hemodynamics. Biomechanical pathophysiological forces including endothelial shear stress—the frictional force generated by blood flow on the vessel wall—are increasingly linked with atherogenesis, vulnerable plaque morphology, and platelet and leukocyte activation. The authors conclude by transitioning from the model of the vulnerable plaque to the concept of the “vulnerable patient,” looking more broadly at physiological contributors to Virchow's triad underpinning acute coronary syndrome.
AB - In this review, the authors explore the evolving evidence linking physiological assessment of coronary artery disease with plaque progression and vulnerability. Reducing adverse clinical events remains the ultimate goal for diagnostic tests, and this review highlights evidence supporting the prognostic value of physiological metrics in predicting outcomes. Historical and contemporary studies support synergy among lesion severity, ischemia, plaque vulnerability, and patient prognosis. Ischemia contributes to clinical events through association with plaque burden, but this review addresses the emerging concept that it associates with atherothrombosis via disturbed lesion hemodynamics. Biomechanical pathophysiological forces including endothelial shear stress—the frictional force generated by blood flow on the vessel wall—are increasingly linked with atherogenesis, vulnerable plaque morphology, and platelet and leukocyte activation. The authors conclude by transitioning from the model of the vulnerable plaque to the concept of the “vulnerable patient,” looking more broadly at physiological contributors to Virchow's triad underpinning acute coronary syndrome.
KW - acute coronary syndromes(s)
KW - coronary physiology
KW - endothelial shear stress
KW - mechanisms of atherosclerosis
KW - plaque vulnerability
UR - http://www.scopus.com/inward/record.url?scp=85039962287&partnerID=8YFLogxK
U2 - 10.1016/j.jcin.2017.08.059
DO - 10.1016/j.jcin.2017.08.059
M3 - Review article
C2 - 29268883
AN - SCOPUS:85039962287
SN - 1936-8798
VL - 10
SP - 2539
EP - 2547
JO - JACC: Cardiovascular Interventions
JF - JACC: Cardiovascular Interventions
IS - 24
ER -