S. Mohlenkamp et al., Minimally invasive evaluation of coronary microvascular function by electron beam computed tomography, CIRCULATION, 102(19), 2000, pp. 2411-2416
Citations number
28
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Background-We previously demonstrated that in vivo electron-beam computed t
omography (EBCT)-based indicator-dilution methods provide an estimate of in
tramyocardial blood volume (BV) and perfusion (F), which relate as BV=aF+b
rootF, where a characterizes the recruitable (exchange) and b the nonrecrui
table (conduit) component of the myocardial microcirculation, In the presen
t study, we compared BV and F with intracoronary Doppler ultrasound-based c
oronary blood flow (CBF) as a method for detecting and quantifying differen
tial responses of these microvascular components to vasoactive drugs in nor
mal (control) and hypercholesterolemic (HC) pigs.
Methods and Results-BV and F values were obtained from contrast-enhanced EB
CT studies in 14 HC and 14 control pigs, BV, F, and CBF values were obtaine
d at baseline (intracoronary infusion of saline) and after 5 minutes each o
f intracoronary infusion of adenosine (100 mug . k(-1) . min(-1)) and nitro
glycerin (40 mu Lg/min). BV and CBF reserves in response to adenosine were
attenuated in HC pigs compared with controls (90+/-36% versus 127+/-42%, P<
0.03, and 485+/-18'% versus 688+/- 160%, P<0.01, respectiveIy). The relatio
nship between BV and F showed consistently lower recruitable BV in HC versu
s control pigs. Nonrecruitable BV reserve in response to adenosine was atte
nuated in HC compared with controls (77+/-20% versus 135+/-28%, P<0.001). O
ur findings are consistent with HC-induced impairment of intramyocardial re
sistance vessel function.
Conclusions--EBCT technology allows minimally invasive evaluation of intram
yocardial microcirculatory function and permits assessment of microvascular
BV distribution in different functional components. This method may be of
value in evaluating the coronary microcirculation in pathophysiological sta
tes such as hypercholesterolemia.