Frequency and clinical implications of fluid dynamically significant diffuse coronary artery disease manifest as graded, longitudinal, base-to-apex myocardial perfusion abnormalities by noninvasive positron emission tomography
Kl. Gould et al., Frequency and clinical implications of fluid dynamically significant diffuse coronary artery disease manifest as graded, longitudinal, base-to-apex myocardial perfusion abnormalities by noninvasive positron emission tomography, CIRCULATION, 101(16), 2000, pp. 1931-1939
Citations number
25
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Background-Diffuse coronary atherosclerosis is the substrate for plaque rup
ture and coronary events. Therefore, in patients with mild arteriographic c
oronary artery disease without significant segmental dipyridamole-induced m
yocardial perfusion defects, we tested the hypothesis that fluid dynamicall
y significant diffuse coronary artery narrowing is frequently manifest as a
graded, longitudinal, base-to-apex myocardial perfusion abnormality by non
invasive PET.
Methods and Results-In this study, 1001 patients with documented coronary a
rtery disease by coronary arteriography showing any visible coronary artery
narrowing underwent rest-dipyridamole PET perfusion imaging. Quantitative
severity of dipyridamole-induced, circumscribed, segmental PET perfusion de
fects was objectively measured by automated software as the minimum quadran
t average relative activity indicating localized flow limiting stenoses. Qu
antitative severity of the graded, longitudinal, base-to-apex myocardial pe
rfusion gradient indicating fluid dynamic effects of diffuse coronary arter
y narrowing was objectively measured by automated software as the spatial s
lope of relative activity along the cardiac longitudinal axis.
Conclusions-In patients with mild arteriographic disease without statistica
lly significant dipyridamole-induced segmental myocardial perfusion defects
caused by flow-limiting stenoses compared with normal control subjects, th
ere was a graded, longitudinal, base-to-apex myocardial perfusion gradient
significantly different from normal control subjects (P=0.001) that was als
o observed for moderate to severe dipyridamole-induced segmental perfusion
defects (P=0.0001), indicating diffuse disease underlying segmental perfusi
on defects; 43% of patients with or without segmental perfusion defects dem
onstrated graded, longitudinal, base-to-apex perfusion abnormalities beyond
+/-2 SD of normal control subjects, indicating diffuse coronary arterial n
arrowing by noninvasive PET perfusion imaging.