Why the study?
Does the eNOS 894T allele affect coronary blood flow at rest and during adenosine-induced hyperemia in individuals without coronary artery disease?
Does the eNOS 894T allele affect coronary blood flow at rest and during adenosine-induced hyperemia in individuals without coronary artery disease?
Homozygous carriers of the eNOS 894T allele exhibit vasomotor dysfunction related to increased microvascular resting tone, though hyperemic response to adenosine remains intact.
Associated with resting microvascular dysfunction in 894T homozygotes; hypothesis-generating for eNOS effects on coronary tone, needs prospective confirmation.
The 894T allele of a G894T polymorphism in the endothelial nitric oxide synthase (eNOS) gene is associated with decreased eNOS activity, cleavage of the protein, and endothelial dysfunction. The present study evaluated the association with coronary blood flow (CBF) at rest and during adenosine (ADO)-induced hyperemia. CBF was determined by Doppler flow wire and angiography in 97 left anterior descending arteries of individuals without coronary artery disease. At rest, average peak velocity (APV) was lower and coronary vascular resistance (CVR) was higher in homozygous carriers of the 894T allele than in heterozygotes and individuals without the 894T allele. CBF tended to be lower in eNOS 894T allele carriers. During ADO-induced hyperemia (18 microg ic), APV, CVR, and CBF were not statistically different between the genotypes. The reduced APV at rest in conjunction with an increased CVR indicates a vasomotor dysfunction related to an increased microvascular resting tone in eNOS 894T allele carriers.
No takes yet. Share an insight, caveat, or question.
Naber et al. (2001) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: