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Circulation
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Published Online
on May 18, 2009

Circulation. 2009
Published online before print May 18, 2009, doi: 10.1161/CIRCULATIONAHA.108.818609
A more recent version of this article appeared on June 2, 2009
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*Substance via MeSH
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*Coronary Artery Disease
*Kawasaki Disease
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Submitted on August 31, 2008
Accepted on March 27, 2009

In Vivo Plaque Composition and Morphology in Coronary Artery Lesions in Adolescents and Young Adults Long After Kawasaki Disease. A Virtual Histology–Intravascular Ultrasound Study

Yoshihide Mitani MD, PhD*, Hiroyuki Ohashi MD, Hirofumi Sawada MD, PhD, Yukiko Ikeyama MD, Hidetoshi Hayakawa MD, PhD, Shin Takabayashi MD, PhD, Kazuo Maruyama MD, PhD, Hideto Shimpo MD, PhD, and Yoshihiro Komada MD, PhD

From the Departments of Pediatrics (Y.M., H.O., H. Sawada, Y.I., H.H., Y.K.), Thoracic Cardiovascular Surgery (S.T., H. Shimpo), and Anesthesiology (K.M.), Mie University Graduate School of Medicine, Tsu, Japan.

* To whom correspondence should be addressed. E-mail: ymitani{at}clin.medic.mie-u.ac.jp.

Background—Coronary artery lesions (CALs) late after Kawasaki disease were characterized by endothelial dysfunction and low-grade inflammation, surrogate markers for atherosclerosis. We tested the hypothesis that CALs in patients long after Kawasaki disease are accompanied by atheroma-like features, as assessed by virtual histology–intravascular ultrasound, a new method to assess coronary plaque composition and morphology in vivo.

Methods and Results—Virtual histology–intravascular ultrasound was performed in 13 Japanese Kawasaki disease patients (median age, 18.3 years; interquartile range, 16.9 to 23.3 years) an interval after Kawasaki disease (median, 15.9 years; interquartile range, 14.3 to 21.9 years). We investigated 6 sites with localized stenosis, 15 sites with an aneurysm, 29 sites with a regressed aneurysm, and 50 sites with a normal coronary segment. Plaque components were categorized into 4 parts: fibrous, fibrofatty, necrotic core, and dense calcium areas. Qualitatively, the normal segment had no or trivial intravascular ultrasound–visible plaque area, whereas the CAL exhibited a heterogeneous plaque area with the 4 components in different amounts and proportions. Quantitatively, a combined group of CALs had a higher absolute value of fibrous, dense calcium, and necrotic core areas than the normal segment. In further analyses of 3 subtypes of CALs, localized stenosis, an advanced lesion, exhibited higher absolute and relative values of dense calcium and necrotic core areas and a lower relative value of the fibrous area than regressed and persistent aneurysms.

Conclusion—The present limited but initial virtual histology–intravascular ultrasound findings give new insight into the potential role of atherogenesis in the evolution of CALs in adolescents and young adults long after Kawasaki disease and therefore warrant further investigation.


Key words: atherosclerosis • coronary disease • imaging • pediatrics • plaque


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