Manlhiot Cedric, Mueller Brigitte, O'Shea Sunita, Majeed Haris, Bernknopf Bailey, Labelle Michael, Westcott Katherine V, Bai Heming, Chahal Nita, Birken Catherine S, Yeung Rae S M, McCrindle Brian W
Labatt Family Heart Centre, Department of Pediatrics, The University of Toronto, Hospital for Sick Children, Toronto, Ontario, Canada.
Division of General Pediatrics, Department of Pediatrics, The University of Toronto, Hospital for Sick Children, Toronto, Ontario, Canada.
PLoS One. 2018 Feb 7;13(2):e0191087. doi: 10.1371/journal.pone.0191087. eCollection 2018.
The pathogenesis of Kawasaki disease (KD) is commonly ascribed to an exaggerated immunologic response to an unidentified environmental or infectious trigger in susceptible children. A comprehensive framework linking epidemiological data and global distribution of KD has not yet been proposed.
Patients with KD (n = 81) were enrolled within 6 weeks of diagnosis along with control subjects (n = 87). All completed an extensive epidemiological questionnaire. Geographic localization software characterized the subjects' neighborhood. KD incidence was compared to atmospheric biological particles counts and winds patterns. These data were used to create a comprehensive risk framework for KD, which we tested against published data on the global distribution. Compared to controls, patients with KD were more likely to be of Asian ancestry and were more likely to live in an environment with low exposure to environmental allergens. Higher atmospheric counts of biological particles other than fungus/spores were associated with a temporal reduction in incidence of KD. Finally, westerly winds were associated with increased fungal particles in the atmosphere and increased incidence of KD over the Greater Toronto Area. Our proposed framework was able to explain approximately 80% of the variation in the global distribution of KD. The main limitations of the study are that the majority of data used in this study are limited to the Canadian context and our proposed disease framework is theoretical and circumstantial rather than the result of a single simulation.
Our proposed etiologic framework incorporates the 1) proportion of population that are genetically susceptible; 2) modulation of risk, determined by habitual exposure to environmental allergens, seasonal variations of atmospheric biological particles and contact with infectious diseases; and 3) exposure to the putative trigger. Future modelling of individual risk and global distribution will be strengthened by taking into consideration all of these non-traditional elements.
川崎病(KD)的发病机制通常归因于易感儿童对未明环境或感染触发因素的过度免疫反应。尚未提出一个将流行病学数据与KD全球分布联系起来的综合框架。
在诊断后6周内纳入了81例KD患者以及87例对照受试者。所有受试者均完成了一份详尽的流行病学调查问卷。地理定位软件对受试者所在社区进行了特征描述。将KD发病率与大气生物颗粒计数及风向模式进行了比较。这些数据被用于创建一个KD综合风险框架,我们根据已发表的全球分布数据对其进行了检验。与对照组相比,KD患者更可能具有亚洲血统,且更可能生活在环境过敏原暴露较低的环境中。除真菌/孢子外的其他生物颗粒在大气中的计数较高与KD发病率的暂时降低相关。最后,西风与大多伦多地区大气中真菌颗粒增加及KD发病率上升相关。我们提出的框架能够解释KD全球分布中约80%的变异。本研究的主要局限性在于,本研究中使用的大多数数据仅限于加拿大的情况,且我们提出的疾病框架是理论性和间接性的,而非单一模拟的结果。
我们提出的病因框架纳入了以下因素:1)遗传易感人群的比例;2)风险调节,由对环境过敏原的习惯性暴露、大气生物颗粒的季节性变化以及与传染病的接触所决定;3)接触假定的触发因素。通过考虑所有这些非传统因素,未来对个体风险和全球分布的建模将得到加强。