» Articles » PMID: 10869266

Active Remodeling of the Coronary Arterial Lesions in the Late Phase of Kawasaki Disease: Immunohistochemical Study

Overview
Journal Circulation
Date 2000 Jun 28
PMID 10869266
Citations 65
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Remodeling of the coronary artery lesions in Kawasaki disease has been observed in longitudinal angiographic studies. However, mechanisms of such remodeling have not yet been elucidated.

Methods And Results: We examined formalin-fixed specimens of the coronary arteries immunohistochemically by using antibodies against vascular growth factors (GFs) and their receptors in 7 children with Kawasaki disease, 9 children with no coronary disease, and 3 adults with atherosclerosis. In the thickened intima at stenotic sites and at recanalized vessels with Kawasaki disease, extensive expression of vascular GFs, such as transforming GF-beta(1), platelet-derived GF-A, and basic fibroblast GF, was observed both within and surrounding smooth muscle cells. Vascular endothelial GF was observed within smooth muscle cells. Furthermore, all of these GFs were strongly expressed in the newly formed microvessels within the intima. In the thinned media, these GFs were focally and weakly expressed. In contrast, these GFs were expressed only in the media in the control children. In cases of adult atherosclerosis, GFs were expressed diffusely in the media but focally and weakly if at all in the intima.

Conclusions: Active remodeling of the coronary artery lesions in Kawasaki disease continues in the form of luxuriant intimal proliferation and neoangiogenesis for several years after the onset of the disease. This process is distinct from adult-onset atherosclerosis.

Citing Articles

Statin suppresses the development of excessive intimal proliferation in a Kawasaki disease mouse model.

Motoji Y, Fukazawa R, Matsui R, Watanabe M, Hashimoto Y, Nagi-Miura N Physiol Rep. 2024; 12(20):e70096.

PMID: 39424429 PMC: 11489001. DOI: 10.14814/phy2.70096.


Whole-exome sequencing reveals Kawasaki disease susceptibility genes and their association with coronary artery lesion.

Wang Y, Chen X, Zhang D, Chen R, Alifu A Front Pediatr. 2024; 12:1400123.

PMID: 39318622 PMC: 11420030. DOI: 10.3389/fped.2024.1400123.


The Central Role of Interleukin-1 Signalling in the Pathogenesis of Kawasaki Disease Vasculitis: Path to Translation.

Atici A, Noval Rivas M, Arditi M Can J Cardiol. 2024; 40(12):2305-2320.

PMID: 39084253 PMC: 11646188. DOI: 10.1016/j.cjca.2024.07.023.


Anterior STEMI in a 25-year-old with Cogan syndrome.

Takla A, Eid F, Eid M, Joshi A, Abtahian F, Cheng A J Cardiol Cases. 2024; 30(1):9-11.

PMID: 39007044 PMC: 11245749. DOI: 10.1016/j.jccase.2024.02.014.


The landscape of hot topics and research frontiers in Kawasaki disease: Scientometric analysis.

Li M, Zheng Z, Yi Q Heliyon. 2024; 10(8):e29680.

PMID: 38660261 PMC: 11040120. DOI: 10.1016/j.heliyon.2024.e29680.