G. Pasterkamp et al., THE IMPACT OF ATHEROSCLEROTIC ARTERIAL REMODELING ON PERCENTAGE OF LUMINAL STENOSIS VARIES WIDELY WITHIN THE ARTERIAL SYSTEM - A POSTMORTEMSTUDY, Arteriosclerosis, thrombosis, and vascular biology, 17(11), 1997, pp. 3057-3063
Luminal stenosis can be based on large atherosclerotic plaques in comp
ensatory enlarged segments or on relatively little plaques in shrunken
segments. In the present study, the contribution of plaque formation
and remodeling to luminal narrowing was compared among six types of ar
teries prone to symptomatic atherosclerosis. Cross-sections (n=5195) w
ere obtained at regular intervals from 329 arteries. For each artery,
the cross-section that contained the least amount of plaque was consid
ered to be the reference. For each cross-section, the percentage of lu
men area decrease was expressed as a percentage of the lumen area at t
he reference site (luminal stenosis). Similarly the area encompassed b
y the internal elastic lamina (IEL area) was expressed as a percentage
of the IEL area at the reference site (relative IEL area). All cross-
sections were categorized in three groups: relative IEL area >105% (en
largement), 95% to 105% (no remodeling), and <95% (shrinkage). The pre
valence of enlargement (50% to 75%) was significantly higher compared
with shrinkage (8% to 25%). Shrinkage was observed most frequently in
the femoral arteries (25%) and infrequently in the renal arteries (8%)
. For all types of arteries, the relative IEL area correlated negative
ly with luminal stenosis (P<.001). Regression analysis of relative IEL
area on luminal stenosis, however, showed significant differences in
the first-order regression coefficients among artery types. On average
, plaque increase was more compensated for by enlargement in the coron
ary, common carotid, and renal arteries compared with the arteries obt
ained from the lower extremities. Anatomic regional differences were o
bserved in the impact of arterial wall remodeling on percent luminal s
tenosis in de novo atherosclerotic lesions.