From the Division of Cardiology, Department of Medicine and the Division
of Cardiothoracic Surgery, Department of Surgery (S.P.), University of
Pittsburgh (Pa) School of Medicine.
Correspondence to Steven E. Reis, MD, University of Pittsburgh Medical Center, 200 Lothrop St, Pittsburgh, PA 15213.
BackgroundTransplant-associated
coronary arteriopathy is manifested in its early stages by
paradoxical coronary artery constriction in response to
endothelium-dependent vasodilator stimuli such as the
cold pressor test (CPT) and is a major cause of death or
retransplantation. Estrogen has vasoactive properties that abolish
coronary artery endothelial dysfunction in
native hearts. We hypothesized that estrogen attenuates inappropriate
coronary artery constriction in cardiac allografts.
Methods and ResultsCoronary artery diameter and systemic
hemodynamic responses to a 90-second CPT were measured
before and 15 minutes after double-blind, randomized administration of
intravenous conjugated estrogens (1.25 mg) or placebo in
men with male cardiac allografts. Before estrogen, 9 men exhibited an
abnormal 15.1±3.0% CPT-induced decrease in coronary artery
diameter. However, repeat CPT did not induce significant
coronary artery constriction when performed 15 minutes after
estrogen. CPT responses before and after estrogen were significantly
different (P=.02). Placebo did not influence
coronary artery responses to CPT in 6 men. Systemic
hemodynamic responses to CPT were not influenced by
estrogen or placebo. Estrogen was the only significant determinant of
changes in coronary artery responses to CPT.
ConclusionsConjugated estrogens acutely abolish abnormal
CPT-induced coronary artery constriction in male cardiac
allografts. This favorable vasomotor effect suggests that estrogen may
prevent inappropriate coronary artery constriction in men with
cardiac transplants.
© 1998 American Heart Association, Inc.
Brief Rapid Communications
Conjugated Estrogens Acutely Abolish Abnormal Cold-Induced Coronary Vasoconstriction in Male Cardiac Allografts
Key Words: transplantation hormones endothelium coronary disease atherosclerosis
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