Coronary endothelial dysfunction after heart transplantation predicts allograft vasculopathy and cardiac death

SM Hollenberg, LW Klein, JE Parrillo, M Scherer… - Circulation, 2001 - Am Heart Assoc
SM Hollenberg, LW Klein, JE Parrillo, M Scherer, D Burns, P Tamburro, M Oberoi…
Circulation, 2001Am Heart Assoc
Background—Coronary endothelial dysfunction may be an early marker for cardiac allograft
vasculopathy (CAV) in orthotopic heart transplant recipients. Using serial studies with
intravascular ultrasound and Doppler flow-wire measurements, we have previously
demonstrated that annual decrements in coronary endothelial function are associated with
progressive intimal thickening. The present study tested whether endothelial dysfunction
predicts subsequent clinical events, including cardiac death and CAV development …
Background Coronary endothelial dysfunction may be an early marker for cardiac allograft vasculopathy (CAV) in orthotopic heart transplant recipients. Using serial studies with intravascular ultrasound and Doppler flow-wire measurements, we have previously demonstrated that annual decrements in coronary endothelial function are associated with progressive intimal thickening. The present study tested whether endothelial dysfunction predicts subsequent clinical events, including cardiac death and CAV development.
Methods and Results Seventy-three patients were studied yearly beginning at transplantation until a prespecified end point was reached. End points were angiographic evidence of CAV (>50% stenosis) or cardiac death (graft failure or sudden death). At each study, coronary endothelial function was measured with intracoronary infusions of adenosine (32-μg bolus), acetylcholine (54 μg over 2 minutes), and nitroglycerin (200 μg) into the left anterior descending coronary artery; intravascular ultrasound images and Doppler velocities were recorded simultaneously. Of the 73 patients studied, 14 reached an end point during the study (6 CAV and 8 deaths, including 4 with known CAV, 1 graft failure, and 3 sudden). On the last study performed, the group with an end point had decreased epicardial (constriction of 11.1±2.9% versus dilation of 1.7±2.2%, P=0.01) and microvascular (flow increase of 75±20% versus 149±16%, P=0.03) endothelium-dependent responses to acetylcholine compared with the patients who did not reach an end point. Responses to adenosine and nitroglycerin did not differ significantly.
Conclusions Endothelial dysfunction, as detected by abnormal responses to acetylcholine, preceded the development of clinical end points. These data implicate endothelial dysfunction in the development of clinically significant vasculopathy and suggest that serial studies of endothelial function have clinical utility.
Am Heart Assoc