Clinical Characteristics of Patients With Kawasaki Disease Whose Siblings Had the Same Disease

被引:5
作者
Hayashida, Kanako [1 ,2 ]
Ae, Ryusuke [1 ]
Masuda, Hiroya [1 ,2 ]
Kosami, Koki [1 ]
Matsumura, Masami [2 ]
Makino, Nobuko [1 ]
Matsubara, Yuri [1 ]
Sasahara, Teppei [1 ]
Nakamura, Yosikazu [1 ]
机构
[1] Jichi Med Univ, Div Publ Hlth, Ctr Community Med, Yakushiji 3311-1, Shimotsuke, Tochigi 3290498, Japan
[2] Jichi Med Univ, Div Gen Med, Ctr Community Med, Shimotsuke, Tochigi, Japan
关键词
Kawasaki disease; sibling; coronary artery abnormality; recurrence; parental history; GENOME-WIDE ASSOCIATION; CORONARY-ARTERY ABNORMALITIES; NATIONWIDE SURVEYS; RISK-FACTORS; SUSCEPTIBILITY; PARENTS; EPIDEMIOLOGY; JAPAN; LOCI;
D O I
10.1097/INF.0000000000003074
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Some patients with Kawasaki disease (KD) have siblings who developed the same disease. Using a large-scale epidemiologic dataset, the present study aimed to determine the clinical characteristics of this population. Methods: We analyzed 89,725 patients diagnosed with KD during 2011-2018 who were registered in the nationwide Japanese KD survey database. Multivariable logistic regression analyses were performed to determine factors associated with sibling history of KD. Results: Of the 89,725 patients, 1777 (2%) had sibling history of KD. Annual prevalence ranged from 1.5% to 2.3% during the study period and showed a tendency toward an increasing trend. Patients with recurrent KD and parental history of KD were significantly associated with sibling history of KD (adjusted odds ratio [95% confidence interval] = 2.15 [1.82-2.54] and 2.64 [2.02-3.47], respectively). Although patients with a sibling history of KD were significantly associated with initial intravenous immunoglobulin treatment resistance (1.14 [1.02-1.28]), no significant association was found between sibling history and coronary artery abnormality development. Among patients with a sibling history of KD, male patients were less likely to have recurrent KD than female patients (0.68 [0.49-0.96]). Conclusions: The significant association between sibling history and parental history may indicate genetic susceptibility to KD onset. Among those with a sibling history, recurrent KD was more likely to occur in female patients. Further studies focusing on this population may contribute toward identification of the cause of KD onset.
引用
收藏
页码:531 / 536
页数:6
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