Pj. Bugelski et al., Nonlinear dynamics in the progression of atherosclerotic fatty streaks: Morphometric analysis, MICROS MICR, 6(6), 2000, pp. 532-541
Atherosclerotic lesions are heterogeneous in terms of their cellular and li
pid composition. While heterogeneity can be the result of stochastic noise,
an alternate hypothesis is that the differences observed among individual
lesions arise from deterministic chaos. Five New Zealand white rabbits were
fed a diet containing 0.15% cholesterol for 6 months. Segments of the aort
a were fixed in formalin, stained en bloc with Nile red (NR) and filipin (F
), and en face fluorescence microscopy was used to map the distribution of
lipids in fatty streaks (FS). The smallest lesions detected stained only wi
th filipin. Larger lesions stained with both Nile red and filipin and two d
istinct regions of Nile red staining, NR-orange (rich in polar lipids) and
NR-yellow (rich in neutral lipids) were observed. Digital overlays revealed
a "nested" arrangement of F, NR-orange, and NR-yellow. The lesions also sh
owed marked heterogeneity in their lipid composition. Thus, although initia
lly similar, as FS increased in size, their composition became divergent, s
uggesting that the ultimate composition of a FS was highly sensitive to its
initial composition. Sensitivity to initial condition is one of the hallma
rks of deterministic systems. To determine if FS were self-similar, another
hallmark of deterministic chaos, the borders of the different regions defi
ned by NR and F staining were subjected to fractal analysis. For each lesio
n, the borders of the F, NR-orange, and NR-yellow regions were found to be
fractal. Return maps were constructed for the differently stained regions.
Analysis of the entire 104-lesion data set showed that although the data co
uld be described by a four-parameter logistic model, the population was not
chaotic. However, return maps drawn for the maxima of the NR-orange staine
d regions demonstrated chaos. Taken together, the data suggest that determi
nistic chaos plays a role in the evolution of atheromatous disease but, in
common with most biologic systems, as the lesions progress, chaotic behavio
r is dampened.