Computational Genomics, IBM T. J. Watson Research Center, New York, USA.
TH Chan Harvard School of Public Health, Harvard University, Cambridge, USA.
Sci Rep. 2021 Jan 11;11(1):408. doi: 10.1038/s41598-020-79745-6.
We sought to investigate whether epidemiological parameters that define epidemic models could be determined from the epidemic trajectory of infections, recovery, and hospitalizations prior to peak, and also to evaluate the comparability of data between jurisdictions reporting their statistics. We found that, analytically, the pre-peak growth of an epidemic underdetermines the model variates, and that the rate limiting variables are dominated by the exponentially expanding eigenmode of their equations. The variates quickly converge to the ratio of eigenvector components of the positive growth mode, which determines the doubling time. Without a sound epidemiological study framework, measurements of infection rates and other parameters are highly corrupted by uneven testing rates, uneven counting, and under reporting of relevant values. We argue that structured experiments must be performed to estimate these parameters in order to perform genetic association studies, or to construct viable models accurately predicting critical quantities such as hospitalization loads.
我们试图研究是否可以从疫情爆发前的感染、康复和住院的流行轨迹中确定定义流行模型的流行病学参数,同时评估报告统计数据的司法管辖区之间的数据可比性。我们发现,从分析的角度来看,疫情爆发前的增长情况并不能确定模型变量,而限制变量的是其方程的指数扩展特征模式。变量会迅速收敛到正增长模式特征向量分量的比值,这决定了倍增时间。如果没有健全的流行病学研究框架,那么对感染率和其他参数的测量会受到不均匀检测率、不均匀计数和相关值漏报的严重影响。我们认为,必须进行结构化实验来估计这些参数,以便进行遗传关联研究,或者构建能够准确预测住院负荷等关键数量的可行模型。