Mizumoto Kenji, Ejima Keisuke, Yamamoto Taro, Nishiura Hiroshi
Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
J Vector Borne Dis. 2014 Sep;51(3):153-64.
BACKGROUND & OBJECTIVES: The present study aimed to systematically quantify the well known risk of severe dengue during secondary infection in literature and to understand how epidemiological mechanisms of enhancement during the secondary infection influence the empirically estimated risk of severe dengue by means of mathematical modeling.
Two conditional risks of severe dengue, i.e. symptomatic illness and dengue hemorrhagic fever (DHF) or dengue shock syndrome (DSS), given secondary infection were explored based on systematically searched prospective studies. A two-strain epidemiological model was employed to simulate the transmission dynamics of dengue and to identify the relevant data gaps in empirical observations.
Using the variance-based weighting, the pooled relative risk (RR) of symptomatic illness during secondary infection was estimated at 9.4 [95% confidence interval (CI): 6.1-14.4], and similarly, RR of DHF/DSS was estimated to be 23.7 (95% CI: 15.3-36.9). A variation in the RR of DHF/DSS was observed among prospective studies. Using the mathematical modeling technique, we identified the duration of cross-protective immunity as an important modulator of the time-dependent behaviour of the RR of severe dengue. Different epidemiological mechanisms of enhancement during secondary infection yielded different RR of severe dengue.
INTERPRETATION & CONCLUSION: Optimal design of prospective cohort study for dengue should be considered, accounting for the time-dependence in the RR during the course of dengue epidemic. It is critical to statistically infer the duration of cross-protective immunity and clarify how the enhancement influences the epidemiological dynamics during secondary infection.
本研究旨在系统地量化文献中已知的二次感染期间严重登革热的风险,并通过数学建模了解二次感染期间增强的流行病学机制如何影响严重登革热的经验估计风险。
基于系统检索的前瞻性研究,探讨了二次感染时严重登革热的两种条件风险,即症状性疾病以及登革出血热(DHF)或登革休克综合征(DSS)。采用两株流行病学模型模拟登革热的传播动态,并确定经验观察中的相关数据缺口。
使用基于方差的加权方法,二次感染期间症状性疾病的合并相对风险(RR)估计为9.4[95%置信区间(CI):6.1 - 14.4],同样,DHF/DSS的RR估计为23.7(95%CI:15.3 - 36.9)。前瞻性研究中观察到DHF/DSS的RR存在差异。使用数学建模技术,我们确定交叉保护性免疫的持续时间是严重登革热RR时间依赖性行为的重要调节因素。二次感染期间不同的增强流行病学机制产生了不同的严重登革热RR。
应考虑登革热前瞻性队列研究的优化设计,同时考虑登革热流行过程中RR的时间依赖性。从统计学上推断交叉保护性免疫的持续时间,并阐明增强如何影响二次感染期间的流行病学动态至关重要。