Public Health Computational and Operations Research (PHICOR), Johns Hopkins Bloomberg School of Public Health, United States; Global Obesity Prevention Center, Johns Hopkins University, United States.
Department of Ecology and Evolutionary Biology, Princeton University, United States.
Epidemics. 2017 Mar;18:81-91. doi: 10.1016/j.epidem.2017.02.004.
Mathematical models can help aid public health responses to Chagas disease. Models are typically developed to fulfill a particular need, and comparing outputs from different models addressing the same question can help identify the strengths and weaknesses of the models in answering particular questions, such as those for achieving the 2020 goals for Chagas disease.
Using two separately developed models (PHICOR/CIDMA model and Princeton model), we simulated dynamics for domestic transmission of Trypanosoma cruzi (T. cruzi). We compared how well the models targeted the last 9 years and last 19 years of the 1968-1998 historical seroprevalence data from Venezuela.
Both models were able to generate the T. cruzi seroprevalence for the next time period within reason to the historical data. The PHICOR/CIDMA model estimates of the total population seroprevalence more closely followed the trends seen in the historic data, while the Princeton model estimates of the age-specific seroprevalence more closely followed historic trends when simulating over 9 years. Additionally, results from both models overestimated T. cruzi seroprevalence among younger age groups, while underestimating the seroprevalence of T. cruzi in older age groups.
The PHICOR/CIDMA and Princeton models differ in level of detail and included features, yet both were able to generate the historical changes in T. cruzi seroprevalence in Venezuela over 9 and 19-year time periods. Our model comparison has demonstrated that different model structures can be useful in evaluating disease transmission dynamics and intervention strategies.
数学模型可以帮助辅助恰加斯病的公共卫生应对。模型通常是为满足特定需求而开发的,比较针对同一问题的不同模型的输出结果,可以帮助确定模型在回答特定问题方面的优势和劣势,例如实现 2020 年恰加斯病目标的问题。
我们使用两个分别开发的模型(PHICOR/CIDMA 模型和普林斯顿模型)模拟了委内瑞拉近距离传播 Trypanosoma cruzi(T. cruzi)的动力学。我们比较了这两个模型在针对委内瑞拉 1968-1998 年历史血清阳性率数据的最后 9 年和最后 19 年的表现。
两个模型都能够在合理的范围内根据历史数据生成下一个时期的 T. cruzi 血清阳性率。PHICOR/CIDMA 模型对总人口血清阳性率的估计更接近历史数据的趋势,而在模拟 9 年以上时,普林斯顿模型对特定年龄组血清阳性率的估计更接近历史趋势。此外,两个模型的结果都高估了年轻年龄组的 T. cruzi 血清阳性率,而低估了老年组的 T. cruzi 血清阳性率。
PHICOR/CIDMA 和普林斯顿模型在详细程度和包含的特征上有所不同,但都能够在 9 年和 19 年的时间内生成委内瑞拉 T. cruzi 血清阳性率的历史变化。我们的模型比较表明,不同的模型结构可以用于评估疾病传播动态和干预策略。