Key result
Children and adolescents with a history of Kawasaki disease had significantly higher carotid intima-media thickness standard deviation scores compared to healthy controls when using an Asian-specific reference (0.60 vs 0.01, p=0.042).
Why the study?
Does a history of Kawasaki disease increase carotid intima-media thickness standard deviation scores compared to healthy controls in children and adolescents?
Systematic Review (n=947)
Does a history of Kawasaki disease increase carotid intima-media thickness standard deviation scores compared to healthy controls in children and adolescents?
Age- and race-specific reference values for CIMT are essential for accurately assessing vascular status and long-term cardiovascular risk in children and adolescents after Kawasaki disease.
Answers are grounded in this paper and cite their sources.
Use of Asian-specific CIMT references may identify vascular changes after Kawasaki disease; leaves open long-term cardiovascular risk implications.
Previous studies that used carotid ultrasound have been largely conflicting in regards to whether or not patients after Kawasaki disease (KD) have a greater carotid intima-media thickness (CIMT) than controls. To test the hypothesis that there are significant differences between the values of CIMT expressed as absolute values and standard deviation scores (SDS) in children and adolescents after KD and controls, we reviewed 12 published articles regarding CIMT on KD patients and controls. The mean ± SD of absolute CIMT (mm) in the KD patients and controls obtained from each article was transformed to SDS (CIMT-SDS) using age-specific reference values established by Jourdan et al. (J: n = 247) and our own data (N: n = 175), and the results among these 12 articles were compared between the two groups and the references for comparison of racial disparities. There were no significant differences in mean absolute CIMT and mean CIMT-SDS for J between KD patients and controls (0.46 ± 0.06 mm vs. 0.44 ± 0.04 mm, p = 0.133, and 1.80 ± 0.84 vs. 1.25 ± 0.12, p = 0.159, respectively). However, there were significant differences in mean CIMT-SDS for N between KD patients and controls (0.60 ± 0.71 vs. 0.01 ± 0.65, p = 0.042). When we assessed the nine articles on Asian subjects, the difference of CIMT-SDS between the two groups was invariably significant only for N (p = 0.015). Compared with the reference values, CIMT-SDS of controls was within the normal range at a rate of 41.6 % for J and 91.6 % for N. These results indicate that age- and race-specific reference values for CIMT are mandatory for performing accurate assessment of the vascular status in healthy children and adolescents, particularly in those after KD considered at increased long-term cardiovascular risk.
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Noto et al. (2015) conducted a systematic review in Kawasaki disease (n=947). History of Kawasaki disease vs. Healthy controls was evaluated on Mean carotid intima-media thickness standard deviation score (CIMT-SDS) using Asian reference values (p=0.042). Children and adolescents with a history of Kawasaki disease had significantly higher carotid intima-media thickness standard deviation scores compared to healthy controls when using an Asian-specific reference (0.60 vs 0.01, p=0.042).
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