Schistosomiasis transmission in Zimbabwe: Modelling based on machine learning

IF 8.8 3区 医学 Q1 Medicine
Hong-Mei Li , Jin-Xin Zheng , Nicholas Midzi , Masceline Jenipher Mutsaka- Makuvaza , Shan Lv , Shang Xia , Ying-jun Qian , Ning Xiao , Robert Berguist , Xiao-Nong Zhou
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引用次数: 0

Abstract

Zimbabwe, located in Southern Africa, faces a significant public health challenge due to schistosomiasis. We investigated this issue with emphasis on risk prediction of schistosomiasis for the entire population. To this end, we reviewed available data on schistosomiasis in Zimbabwe from a literature search covering the 1980-2022 period considering the potential impact of 26 environmental and socioeconomic variables obtained from public sources. We studied the population requiring praziquantel with regard to whether or not mass drug administration (MDA) had been regularly applied. Three machine-learning algorithms were tested for their ability to predict the prevalence of schistosomiasis in Zimbabwe based on the mean absolute error (MAE), the root mean squared error (RMSE) and the coefficient of determination (R2). The findings revealed different roles of the 26 factors with respect to transmission and there were particular variations between Schistosoma haematobium and S. mansoni infections. We found that the top-five correlation factors, such as the past (rather than current) time, unsettled MDA implementation, constrained economy, high rainfall during the warmest season, and high annual precipitation were closely associated with higher S. haematobium prevalence, while lower elevation, high rainfall during the warmest season, steeper slope, past (rather than current) time, and higher minimum temperature in the coldest month were rather related to higher S. mansoni prevalence. The random forest (RF) algorithm was considered as the formal best model construction method, with MAE = 0.108; RMSE = 0.143; and R2 = 0.517 for S. haematobium, and with the corresponding figures for S. mansoni being 0.053; 0.082; and 0.458. Based on this optimal model, the current total schistosomiasis prevalence in Zimbabwe under MDA implementation was 19.8%, with that of S. haematobium at 13.8% and that of S. mansoni at 7.1%, requiring annual MDA based on a population of 3,003,928. Without MDA, the current total schistosomiasis prevalence would be 23.2%, that of S. haematobium 17.1% and that of S. mansoni prevalence at 7.4%, requiring annual MDA based on a population of 3,521,466. The study reveals that MDA alone is insufficient for schistosomiasis elimination, especially that due to S. mansoni. This study predicts a moderate prevalence of schistosomiasis in Zimbabwe, with its elimination requiring comprehensive control measures beyond the currently used strategies, including health education, snail control, population surveillance and environmental management.

津巴布韦的血吸虫病传播:基于机器学习的建模
津巴布韦位于非洲南部,因血吸虫病而面临着重大的公共卫生挑战。我们对这一问题进行了调查,重点是对整个人口的血吸虫病风险进行预测。为此,我们通过文献检索回顾了 1980-2022 年期间津巴布韦血吸虫病的现有数据,考虑了从公共来源获得的 26 个环境和社会经济变量的潜在影响。我们研究了需要使用吡喹酮的人群是否定期使用大规模药物管理 (MDA)。根据平均绝对误差 (MAE)、均方根误差 (RMSE) 和判定系数 (R2),测试了三种机器学习算法预测津巴布韦血吸虫病流行率的能力。研究结果表明,26 个因素在传播方面的作用各不相同,血吸虫和曼氏血吸虫感染之间的差异尤为明显。我们发现,前五大相关因素,如过去(而非当前)时间、MDA 实施情况不稳定、经济受限、最暖季节降雨量大、年降水量大与血吸虫感染率较高密切相关,而海拔较低、最暖季节降雨量大、坡度较陡、过去(而非当前)时间、最冷月最低气温较高与曼森氏血吸虫感染率较高相当相关。随机森林(RF)算法被认为是正式的最佳模型构建方法,对于血吸虫的 MAE = 0.108;RMSE = 0.143;R2 = 0.517,而对于曼氏沙门氏菌的相应数字分别为 0.053、0.082 和 0.458。根据这一最佳模型,在实施 MDA 的情况下,津巴布韦目前的血吸虫病总流行率为 19.8%,其中血吸虫为 13.8%,曼森尼为 7.1%,按 3,003,928 人计算,需要每年进行 MDA。如果没有 MDA,目前血吸虫病的总流行率将为 23.2%,血吸虫的流行率为 17.1%,曼氏血吸虫病的流行率为 7.4%,按 3,521,466 人计算,需要每年进行 MDA。这项研究表明,仅靠药物滥用和杀虫剂不足以消灭血吸虫病,尤其是曼森氏杆菌引起的血吸虫病。这项研究预测血吸虫病在津巴布韦的流行率为中等,要消灭血吸虫病,除了目前使用的策略外,还需要采取全面的控制措施,包括健康教育、钉螺控制、人口监测和环境管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Infectious Disease Modelling
Infectious Disease Modelling Mathematics-Applied Mathematics
CiteScore
17.00
自引率
3.40%
发文量
73
审稿时长
17 weeks
期刊介绍: Infectious Disease Modelling is an open access journal that undergoes peer-review. Its main objective is to facilitate research that combines mathematical modelling, retrieval and analysis of infection disease data, and public health decision support. The journal actively encourages original research that improves this interface, as well as review articles that highlight innovative methodologies relevant to data collection, informatics, and policy making in the field of public health.
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