Abstract
An error in a previous publication in the calculation of the average age at first infection for the model is corrected here. The average age at first infection for the effective contact rates used to generate the data ranges from 1.2 to 3.3 years of age instead of 3–5 years of age as advertised in the previous version of the paper. This change has an effect on the force of infection generated by this model. In this corrigendum, we demonstrate the correct method to calculate the average age at first infection for the model. We compare the forces of infection that correspond to these ages in our model with the forces of infection in other endemic populations. We show that the modified age range corresponds to forces of infection which are higher than those that are known to exist in historical studies of polio-endemic regions. Thus, the results in the paper have limited applicability to real-world endemic situations.
Keywords: Poliovirus, Silent circulation, Acute flaccid paralysis surveillance, Microsimulation model, Gillespie algorithm
1. Introduction
The average age at first infection is an important quantity in epidemiological modeling since it is incorporated in many instances of reported data. It is particularly noteworthy if the disease has asymptomatic presentation after the first infection as is the case with polio. Even if the model has no age structure, the average age at first infection can be determined. In 1974, Dietz Dietz (1974) constructed the formula for the average age at first infection in a S-I-R compartmental model with permanent immunity. In Vallejo, Keesling, Koopman, and Singer (2017), the formula by Dietz Dietz (1974) was mistakenly used to calculate the average age at first infection in a model that had temporary immunity. In this corrigendum, we demonstrate the correct method by which to calculate the average age at first infection for the model given in Vallejo et al. (2017). We can use the average age at first infection to calculate the force of infection for the population.
2. Calculating the average age at first infection in a model with temporary immunity
The differential equations model that is related to the stochastic model presented in Vallejo et al. (2017) is given in equation (1). Movement from the S compartment to the compartment represents the first infection. Thus, the inverse of the force of infection term at equilibrium is the average time spent in the susceptible compartment before the first infection occurs, where and are the equilibrium values of the and equations, respectively. In a model without age-structure, this is the definition of the average age at first infection.
(1) |
Using the parameter values given in Vallejo et al. (2017), the average age at first infection can be calculated for each population size, β value, and waning immunity scenario. These results are presented in Table 1. Note that, in general, the average age at first infection is largest at the smallest β value under the slow-deep waning immunity scenario. The relationship between the average age at first infection and the population size is not strictly increasing or decreasing due to round-off error when calculating the equilibrium values of the and compartments.
Table 1.
β Value | Type of Waning Immunity | Population Size |
|||
---|---|---|---|---|---|
N = 3500 | N = 5000 | N = 7000 | N = 10,000 | ||
135 | fast-shallow | 3.11 | 3.08 | 3.11 | 3.14 |
intermediate | 3.16 | 3.23 | 3.16 | 3.23 | |
slow-deep | 3.10 | 3.3 | 3.26 | 3.18 | |
200 | fast-shallow | 1.82 | 1.7 | 1.82 | 1.76 |
intermediate | 1.98 | 2.07 | 2.06 | 1.98 | |
slow-deep | 2.09 | 2.07 | 2.09 | 2.06 | |
260 | fast-shallow | 1.29 | 1.21 | 1.23 | 1.26 |
intermediate | 1.52 | 1.47 | 1.52 | 1.4 | |
slow-deep | 1.61 | 1.6 | 1.6 | 1.53 |
3. Force of infection comparison
Fine et al. Fine and Carneiro (1999) reconstructed the values for several populations ranging from those in developing nations to those in industrialized nations using age-specific seroprevalence data and age-structured demographic data. Since this data was primarily collected in the 1950s, these historical studies reflect populations in which polio was endemic. Using the formula that relates the force of infection to the value in a model with permanent immunity as constructed by Dietz Dietz (1974), we have derived the force of infection for each study population represented in Fine and Carneiro (1999) using the value (see Fig. 1 in Fine and Carneiro (1999)). The force of infection in a model of an endemic population should fall in the range generated by the study populations in Fine and Carneiro (1999). We compare the force of infection generated in our model with those from Fine and Carneiro (1999). (Fig. 1). The force of infection in our model is calculated by taking the inverse of the average age at first infection at equilibrium. Since there are a range of values for the force of infection for each value, to make the comparison between our model and the forces of infection calculated using the values in Fine and Carneiro (1999), we take the average of the forces of infection generated for each value. The results are given in Fig. 1. It is clear that the forces of infection generated using the parameters in our model are outside of the range given in Fine and Carneiro (1999). This implies that the model results have limited applicability to regions of endemic polio.
4. Discussion and conclusion
Accounting for the temporary immunity in Vallejo et al. (2017) had the effect of decreasing the average age of first infection. In a model of this form, a decrease in the average age at first infection corresponded to an increase in the force of infection. With the parameter values chosen, the forces of infection in Vallejo et al. (2017) are considerably out of the range of forces of infection observed in historical studies of polio-endemic regions. Thus, the conclusions that can be drawn from the paper must be interpreted with caution as they may not have application to regions in which polio is currently endemic.
Handling Editor: Jianhong Wu
Footnotes
Peer review under responsibility of KeAi Communications Co., Ltd.
Contributor Information
Celeste Vallejo, Email: cvallejo@ufl.edu.
James Keesling, Email: kees@ufl.edu.
James Koopman, Email: jkoopman@umich.edu.
Burton Singer, Email: bhsinger@epi.ufl.edu.
References
- Dietz K. Proceedings of the society for industrial and applied Mathematics, Epidemiology: Philadelphia. 1974. Transmission and control of arbovirus diseases. [Google Scholar]
- Fine P.E., Carneiro I.A.M. Transmissibility and persistence of oral polio vaccine Viruses: Implications for the global poliomyelitis eradication initiative. American Journal of Epidemiology. 1999;150(10):1001–1021. doi: 10.1093/oxfordjournals.aje.a009924. [DOI] [PubMed] [Google Scholar]
- Nations U. 2004. World population prospects: The 2002 revision. ST/ESA/SER.A/233. [Google Scholar]
- Vallejo C., Keesling J., Koopman J., Singer B. Silent circulation of poliovirus in small populations. Infectious Disease Modelling. 2017;(2017) doi: 10.1016/j.idm.2017.11.001. [DOI] [PMC free article] [PubMed] [Google Scholar]