• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

疟原虫 vivax 建模:复发、治疗、季节性和 G6PD 缺乏症。

Modeling Plasmodium vivax: relapses, treatment, seasonality, and G6PD deficiency.

机构信息

Department of Mathematics, University of Miami, Coral Gables, Miami, FL 33124-4250, USA.

出版信息

J Theor Biol. 2013 Jan 7;316:25-34. doi: 10.1016/j.jtbi.2012.08.024. Epub 2012 Aug 29.

DOI:10.1016/j.jtbi.2012.08.024
PMID:22959914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3728673/
Abstract

Plasmodium vivax (P. vivax) is one of the most important human malaria species that is geographically widely endemic and causes social and economic burden globally. However, its consequences have long been neglected and underestimated as it has been mistakenly considered a benign and inconsequential malaria species as compared to Plasmodium falciparum. One of the important differences between P. falciparum and P. vivax is the formation of P. vivax latent-stage parasites (hypnozoites) that can cause relapses after a course of treatment. In this work, mathematical modeling is employed to investigate how patterns of incubation periods and relapses of P. vivax, variation in treatment, and seasonal abundance of mosquitoes influence the number of humans infected with P. vivax and the mean age at infection of humans in tropical and temperate regions. The model predicts that: (i) the number of humans infected with P. vivax may increase when an incubation period of parasites in humans and a latent period of hypnozoites decrease; (ii) without primaquine, the only licensed drug to prevent relapses, P. vivax may be highly prevalent; (iii) the mean age at infection of humans may increase when a latent period of hypnozoites increases; (iv) the number of infectious humans may peak at a few months before the middle of each dry season and the number of hypnozoite carriers may peak at nearly the middle of each dry season. In addition, glucose-6-phosphate-dehydrogenase (G6PD) deficiency, which is the most common enzyme defect in humans that may provide some protection against P. vivax infection and severity, is taken into account to study its impact on the number of humans infected with P. vivax. Modeling results indicate that the increased number of infected humans may result from a combination of a larger proportion of humans with G6PD deficiency in the population, a lesser protection of G6PD deficiency to P. vivax infection, and a shorter latent period of hypnozoites.

摘要

间日疟原虫(P. vivax)是最重要的人类疟疾物种之一,其分布广泛,在全球范围内造成社会和经济负担。然而,由于其长期以来被误认为是比恶性疟原虫(Plasmodium falciparum)更为良性和无足轻重的疟疾物种,因此其后果一直被忽视和低估。恶性疟原虫和间日疟原虫的一个重要区别是间日疟原虫潜伏期寄生虫(休眠子)的形成,这些寄生虫在治疗后会引起复发。在这项工作中,我们采用数学建模来研究间日疟潜伏期和复发模式、治疗方法的变化以及蚊子季节性丰度如何影响感染间日疟原虫的人数以及热带和温带地区人类感染的平均年龄。模型预测:(i)当人体寄生虫潜伏期和休眠子潜伏期减小时,感染间日疟原虫的人数可能会增加;(ii)如果没有预防复发的唯一许可药物伯氨喹,间日疟原虫的流行率可能会很高;(iii)当休眠子潜伏期增加时,人类感染的平均年龄可能会增加;(iv)在每个旱季中期前的几个月,传染性人类数量可能达到峰值,休眠子携带者数量可能在每个旱季中期达到峰值。此外,葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症,这是人类最常见的酶缺陷,可能对间日疟原虫感染和严重程度提供一定的保护,我们也考虑了它对感染间日疟原虫的人数的影响。建模结果表明,感染人数的增加可能是由于人群中 G6PD 缺乏症的比例增加、G6PD 缺乏症对间日疟原虫感染的保护作用降低以及休眠子潜伏期缩短的综合作用所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/83ddebd1cc93/nihms414845f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/d0bee2894fca/nihms414845f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/f1ec239f876e/nihms414845f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/4db6cc9f40b9/nihms414845f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/bb9bf064b190/nihms414845f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/83ddebd1cc93/nihms414845f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/d0bee2894fca/nihms414845f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/f1ec239f876e/nihms414845f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/4db6cc9f40b9/nihms414845f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/bb9bf064b190/nihms414845f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0d/3728673/83ddebd1cc93/nihms414845f5.jpg

相似文献

1
Modeling Plasmodium vivax: relapses, treatment, seasonality, and G6PD deficiency.疟原虫 vivax 建模:复发、治疗、季节性和 G6PD 缺乏症。
J Theor Biol. 2013 Jan 7;316:25-34. doi: 10.1016/j.jtbi.2012.08.024. Epub 2012 Aug 29.
2
Kinetics of glucose-6-phosphate dehydrogenase (G6PD) activity during Plasmodium vivax infection: implications for early radical malaria treatment.葡萄糖-6-磷酸脱氢酶(G6PD)活性在间日疟原虫感染期间的动力学:对早期根治性疟疾治疗的影响。
Malar J. 2024 May 9;23(1):140. doi: 10.1186/s12936-024-04973-4.
3
Population-level estimates of the proportion of Plasmodium vivax blood-stage infections attributable to relapses among febrile patients attending Adama Malaria Diagnostic Centre, East Shoa Zone, Oromia, Ethiopia.在埃塞俄比亚奥罗米亚州东绍阿地区阿达马疟疾诊断中心就诊的发热患者中,间日疟原虫血期感染归因于复发的比例的人群水平估计。
Malar J. 2017 Jul 27;16(1):301. doi: 10.1186/s12936-017-1944-3.
4
Modelling the contribution of the hypnozoite reservoir to Plasmodium vivax transmission.模拟潜隐体库对间日疟原虫传播的贡献。
Elife. 2014 Nov 18;3:e04692. doi: 10.7554/eLife.04692.
5
[Role of primaquine in malaria control and elimination in French-speaking Africa].[伯氨喹在非洲法语区疟疾控制与消除中的作用]
Bull Soc Pathol Exot. 2017 Aug;110(3):198-206. doi: 10.1007/s13149-017-0556-z. Epub 2017 Apr 17.
6
Primaquine ineligibility in anti-relapse therapy of Plasmodium vivax malaria: the problem of G6PD deficiency and cytochrome P-450 2D6 polymorphisms.在间日疟原虫抗复发治疗中禁用伯氨喹:G6PD 缺乏症和细胞色素 P-450 2D6 多态性的问题。
Malar J. 2018 Jan 22;17(1):42. doi: 10.1186/s12936-018-2190-z.
7
Epidemiology and Control of Plasmodium vivax in Afghanistan.阿富汗间日疟原虫的流行病学与防控
Am J Trop Med Hyg. 2016 Dec 28;95(6 Suppl):72-77. doi: 10.4269/ajtmh.16-0172. Epub 2016 Oct 5.
8
Investigation of glucose-6-phosphate dehydrogenase (G6PD) deficiency prevalence in a Plasmodium vivax-endemic area in the Republic of Korea (ROK).韩国(ROK)间日疟流行区葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症的流行情况调查。
Malar J. 2020 Sep 1;19(1):317. doi: 10.1186/s12936-020-03393-4.
9
The impact of phenotypic and genotypic G6PD deficiency on risk of plasmodium vivax infection: a case-control study amongst Afghan refugees in Pakistan.表型和基因型 G6PD 缺乏症对间日疟原虫感染风险的影响:巴基斯坦阿富汗难民中的病例对照研究。
PLoS Med. 2010 May 25;7(5):e1000283. doi: 10.1371/journal.pmed.1000283.
10
Variation in relapse frequency and the transmission potential of Plasmodium vivax malaria.间日疟原虫疟疾复发频率及传播潜力的变化
Proc Biol Sci. 2016 Mar 30;283(1827):20160048. doi: 10.1098/rspb.2016.0048.

引用本文的文献

1
Co-design of a routine clinical review to improve the safety of high dose radical cure treatment for Plasmodium vivax malaria: findings from Cambodia and Ethiopia.共同设计常规临床评估以提高间日疟原虫疟疾高剂量根治治疗的安全性:来自柬埔寨和埃塞俄比亚的研究结果
Malar J. 2025 May 28;24(1):171. doi: 10.1186/s12936-025-05425-3.
2
Implementation of Glucose-6-Phosphate Dehydrogenase (G6PD) testing for Plasmodium vivax case management, a mixed method study from Cambodia.用于间日疟原虫病例管理的葡萄糖-6-磷酸脱氢酶(G6PD)检测的实施:一项来自柬埔寨的混合方法研究
PLOS Glob Public Health. 2024 Jul 19;4(7):e0003476. doi: 10.1371/journal.pgph.0003476. eCollection 2024.
3

本文引用的文献

1
Modeling the effects of relapse in the transmission dynamics of malaria parasites.疟原虫传播动力学中复发影响的建模。
J Parasitol Res. 2012;2012:921715. doi: 10.1155/2012/921715. Epub 2011 Sep 28.
2
Duffy negative antigen is no longer a barrier to Plasmodium vivax--molecular evidences from the African West Coast (Angola and Equatorial Guinea).达菲阴性抗原不再是阻碍间日疟原虫传播的障碍——来自非洲西海岸(安哥拉和赤道几内亚)的分子证据。
PLoS Negl Trop Dis. 2011 Jun;5(6):e1192. doi: 10.1371/journal.pntd.0001192. Epub 2011 Jun 21.
3
Establishment of an in vitro assay for assessing the effects of drugs on the liver stages of Plasmodium vivax malaria.
Mathematical models of Plasmodium vivax transmission: A scoping review.
《疟原虫 vivax 传播的数学模型:范围综述》。
PLoS Comput Biol. 2024 Mar 14;20(3):e1011931. doi: 10.1371/journal.pcbi.1011931. eCollection 2024 Mar.
4
Quantifying the impact of interventions against Plasmodium vivax: A model for country-specific use.量化针对间日疟原虫的干预措施的影响:一种供各国具体使用的模型。
Epidemics. 2024 Mar;46:100747. doi: 10.1016/j.epidem.2024.100747. Epub 2024 Feb 5.
5
Superinfection and the hypnozoite reservoir for Plasmodium vivax: a general framework.疟原虫 vivax 的继发感染和休眠子库:一个通用框架。
J Math Biol. 2023 Dec 1;88(1):7. doi: 10.1007/s00285-023-02014-3.
6
Optimal Interruption of P. vivax Malaria Transmission Using Mass Drug Administration.采用大规模药物治疗中断间日疟传播的最适策略。
Bull Math Biol. 2023 Apr 19;85(6):43. doi: 10.1007/s11538-023-01153-4.
7
Evolutionary genetics of malaria.疟疾的进化遗传学
Front Genet. 2022 Nov 3;13:1030463. doi: 10.3389/fgene.2022.1030463. eCollection 2022.
8
Assessing the Impact of Relapse, Reinfection and Recrudescence on Malaria Eradication Policy: A Bifurcation and Optimal Control Analysis.评估复发、再感染和复燃对疟疾根除政策的影响:分岔与最优控制分析
Trop Med Infect Dis. 2022 Sep 24;7(10):263. doi: 10.3390/tropicalmed7100263.
9
A Multiscale Mathematical Model of Plasmodium Vivax Transmission.《恶性疟原虫传播的多尺度数学模型》
Bull Math Biol. 2022 Jul 1;84(8):81. doi: 10.1007/s11538-022-01036-0.
10
Duffy blood system and G6PD genetic variants in vivax malaria patients from Manaus, Amazonas, Brazil.巴西亚马逊州玛瑙斯的间日疟患者中的 Duffy 血型系统和 G6PD 遗传变异。
Malar J. 2022 May 8;21(1):144. doi: 10.1186/s12936-022-04165-y.
建立一种体外检测方法,用于评估药物对间日疟原虫肝期的影响。
PLoS One. 2010 Dec 9;5(12):e14275. doi: 10.1371/journal.pone.0014275.
4
Efficacy and safety of chloroquine for treatment in patients with uncomplicated Plasmodium vivax infections in endemic countries.在疟疾流行国家,氯喹治疗无并发症间日疟原虫感染的疗效和安全性。
Trans R Soc Trop Med Hyg. 2010 Nov;104(11):695-705. doi: 10.1016/j.trstmh.2010.08.009. Epub 2010 Sep 20.
5
The international limits and population at risk of Plasmodium vivax transmission in 2009.2009 年按蚊传播间日疟原虫的国际界限和危险人群。
PLoS Negl Trop Dis. 2010 Aug 3;4(8):e774. doi: 10.1371/journal.pntd.0000774.
6
Population screening for glucose-6-phosphate dehydrogenase deficiencies in Isabel Province, Solomon Islands, using a modified enzyme assay on filter paper dried bloodspots.采用滤纸干血斑改良酶分析法在所罗门群岛伊莎贝尔省进行葡萄糖-6-磷酸脱氢酶缺乏症的人群筛查。
Malar J. 2010 Aug 5;9:223. doi: 10.1186/1475-2875-9-223.
7
The dilution effect of the domestic animal population on the transmission of P. vivax malaria.家养动物种群对间日疟原虫传播的稀释效应。
J Theor Biol. 2010 Sep 21;266(2):299-306. doi: 10.1016/j.jtbi.2010.06.032. Epub 2010 Jul 7.
8
The impact of phenotypic and genotypic G6PD deficiency on risk of plasmodium vivax infection: a case-control study amongst Afghan refugees in Pakistan.表型和基因型 G6PD 缺乏症对间日疟原虫感染风险的影响:巴基斯坦阿富汗难民中的病例对照研究。
PLoS Med. 2010 May 25;7(5):e1000283. doi: 10.1371/journal.pmed.1000283.
9
Analysis of a vector-bias model on malaria transmission.疟疾传播的向量偏倚模型分析。
Bull Math Biol. 2011 Mar;73(3):639-57. doi: 10.1007/s11538-010-9545-0. Epub 2010 May 22.
10
Positively selected G6PD-Mahidol mutation reduces Plasmodium vivax density in Southeast Asians.正向选择的 G6PD-Mahidol 突变降低东南亚人群中的间日疟原虫密度。
Science. 2009 Dec 11;326(5959):1546-9. doi: 10.1126/science.1178849.