Zhao Xiahong, Siegel Karen, Chen Mark I-Cheng, Cook Alex R
Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore.
Communicable Disease Centre, Tan Tock Seng Hospital, Singapore.
Influenza Other Respir Viruses. 2017 May;11(3):202-210. doi: 10.1111/irv.12452. Epub 2017 Apr 26.
For pathogens such as influenza that cause many subclinical cases, serologic data can be used to estimate attack rates and the severity of an epidemic in near real time. Current methods for analysing serologic data tend to rely on use of a simple threshold or comparison of titres between pre- and post-epidemic, which may not accurately reflect actual infection rates.
We propose a method for quantifying infection rates using paired sera and bivariate probit models to evaluate the accuracy of thresholds currently used for influenza epidemics with low and high existing herd immunity levels, and a subsequent non-influenza period. Pre- and post-epidemic sera were taken from a cohort of adults in Singapore (n=838). Bivariate probit models with latent titre levels were fit to the joint distribution of haemagglutination-inhibition assay-determined antibody titres using Markov chain Monte Carlo simulation.
Estimated attack rates were 15% (95% credible interval: 12%-19%) for the first H1N1 pandemic wave. For a large outbreak due to a new strain, a threshold of 1:20 and a twofold rise (if pared sera is available) would result in a more accurate estimate of incidence.
The approach presented here offers the basis for a reconsideration of methods used to assess diagnostic tests by both reconsidering the thresholds used and by analysing serological data with a novel statistical model.
对于诸如流感这类会导致许多亚临床病例的病原体,血清学数据可用于近乎实时地估计感染率和疫情的严重程度。当前分析血清学数据的方法往往依赖于使用简单阈值或比较疫情前后的滴度,而这可能无法准确反映实际感染率。
我们提出一种使用配对血清和双变量概率模型来量化感染率的方法,以评估当前用于不同现有群体免疫水平的流感疫情以及随后非流感时期的阈值的准确性。疫情前后的血清取自新加坡一组成年人(n = 838)。使用马尔可夫链蒙特卡罗模拟,将具有潜在滴度水平的双变量概率模型拟合到血凝抑制试验确定的抗体滴度的联合分布。
在甲型H1N1流感大流行的第一波中,估计感染率为15%(95%可信区间:12% - 19%)。对于由新毒株引起的大规模疫情,1:20的阈值和两倍的上升幅度(如果有配对血清)将导致对发病率的更准确估计。
本文提出的方法为重新考虑评估诊断测试的方法提供了基础,既可以通过重新考虑所使用的阈值,也可以通过使用新的统计模型分析血清学数据来实现。