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Subclinical arterial stiffness in young children after Kawasaki disease

Published online by Cambridge University Press:  07 February 2013

Masato Oguri
Affiliation:
Department of Pediatrics, Kanazawa Medical University, Ishikawa, Japan
Tsuneyuki Nakamura*
Affiliation:
Department of Pediatrics, Kanazawa Medical University, Ishikawa, Japan Department of Pediatrics, Division of Cardiology, Children's Hospital Los Angeles, Los Angeles, United States of America
Keita Tamanuki
Affiliation:
Department of Pediatrics, Kanazawa Medical University, Ishikawa, Japan
Chisato Akita
Affiliation:
Department of Pediatrics, Kanazawa Medical University, Ishikawa, Japan
Chika Kitaoka
Affiliation:
Department of Pediatrics, Kanazawa Medical University, Ishikawa, Japan
Yutaka Saikawa
Affiliation:
Department of Pediatrics, Kanazawa Medical University, Ishikawa, Japan
Masato Takahashi
Affiliation:
Department of Pediatrics, Division of Cardiology, Children's Hospital Los Angeles, Los Angeles, United States of America
*
Correspondence to: Dr T. Nakamura, MD, PhD, Department of Pediatrics, Kanazawa Medical University, 1-1 Daigaku, Uchinada, Kahoku, Ishikawa 920-0293, Japan. Tel: +81-76-286-3511; Fax: +81-76-286-8918; E-mail: p-tune@kanazawa-med.ac.jp
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Abstract

Background

Recent studies have revealed that atherosclerosis progresses faster than expected in young adults with a history of Kawasaki disease. However, it is unclear as to when these arterial changes become measurable. In this study, we evaluated subclinical arterial stiffness in young children with a history of Kawasaki disease using two-dimensional ultrasound speckle tracking.

Methods

A total of 75 children with a history of Kawasaki disease (mean age, 8.2 ± 2.8 years) and 50 healthy controls (mean age 8.3 ± 3.5 years) were included. The two regions of interest for speckle tracking were manually positioned at the anterior and posterior carotid arterial wall using a Philips iE33 (Philips Medical Systems, Bothell, WA, USA). The peak systolic strain, time to peak systolic strain, early systolic strain rate, and late systolic strain rate were continuously monitored between the two regions of interest. Furthermore, the intimal-medial thickness, stiffness β, and pressure-elastic modulus, as conventional measures of arterial stiffness, were concurrently obtained.

Results

The peak systolic strain and late systolic strain rate differed significantly between the patients with Kawasaki disease and controls (6.69% versus 8.60%, p < 0.01, and −0.28/second versus −0.51/second, p < 0.0001, respectively). There was no difference in the time to peak systolic strain, early systolic strain rate, and conventional measures.

Conclusions

The arteries of patients with Kawasaki disease appear to develop mild sclerotic changes shortly after the onset of the disease.

Information

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2013 
Figure 0

Figure 1 Two-point strain method. (a) two regions of interest are located on the opposite walls of the carotid artery, (b) strain curves, and (c) strain rate curves. 1, the peak systolic strain is the maximum rate of change over circumferential length at QRS onset; 2, the peak systolic strain time is the interval from the beginning of QRS to the point of maximum rate-of-change; 3, the early systolic strain rate is the maximum positive speed of deformation in the early LV ejection time; and 4, the late systolic strain rate is the maximum negative speed of deformation in the late LV ejection time. CCA = common carotid artery; LV = left ventricle.

Figure 1

Table 1 Characteristics of the enrolled subjects.

Figure 2

Table 2 Characteristics of Kawasaki disease patients.

Figure 3

Table 3 Parameters of arteriosclerosis.

Figure 4

Figure 2 Association between the new method and intimal-medial thickness. (a) Simple linear regression between peak systolic strain and IMT and (b) simple linear regression between the late negative strain rate and IMT; filled circles represent patients with Kawasaki disease and open circles represent control patients. The solid line represents simple linear regression throughout the data. IMT = intimal-medial thickness.

Figure 5

Figure 3 Association between the new method and stiffness β. (a) Simple linear regression between peak systolic strain and stiffness β and (b) simple linear regression between the late negative strain rate and stiffness β; filled circles represent patients with Kawasaki disease and open circles represent control patients. The solid line represents simple linear regression throughout the data.

Figure 6

Figure 4 Association between the new method and pressure-elastic modulus. (a) Simple linear regression between peak systolic strain and pressure-elastic modulus and (b) simple linear regression between the late negative strain rate and pressure-elastic modulus, Ep; filled circles represent patients with Kawasaki disease and open circles represent control patients. The solid line represents simple linear regression throughout the data. Ep = pressure-elastic modulus.

Figure 7

Table 4a The forced-entry multiple regression response variable: peak systolic strain (n = 75).

Figure 8

Table 4b The forced-entry multiple regression response variable: late systolic strain rate (n = 75).

Figure 9

Figure 5 Association of age and the new methods. (a) Simple linear regression between peak systolic strain and age and (b) simple linear regression between the late negative strain rate and age; filled circles represent patients with Kawasaki disease and open circles represent control patients. The solid line represents linear regression through the Kawasaki disease data and the dotted line represents linear regression through the control. On comparing the regression slopes between the two groups, there were no significant differences in the slopes of the peak systolic strain or late systolic strain rates between those with Kawasaki disease and normal controls.