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本文引用的文献

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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.
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Pharmacokinetics of artemether-lumefantrine and artesunate-amodiaquine in children in Kampala, Uganda.乌干达坎帕拉儿童中蒿甲醚-本芴醇和青蒿琥酯-阿莫地喹的药代动力学。
Antimicrob Agents Chemother. 2010 Jan;54(1):52-9. doi: 10.1128/AAC.00679-09. Epub 2009 Oct 19.
3
Key gaps in the knowledge of Plasmodium vivax, a neglected human malaria parasite.间日疟原虫,一种被忽视的人类疟原虫,在知识方面存在关键空白。
Lancet Infect Dis. 2009 Sep;9(9):555-66. doi: 10.1016/S1473-3099(09)70177-X.
4
High prevalence and fixation of Plasmodium vivax dhfr/dhps mutations related to sulfadoxine/pyrimethamine resistance in French Guiana.法属圭亚那间日疟原虫二氢叶酸还原酶/二氢蝶酸合酶突变与磺胺多辛/乙胺嘧啶耐药性相关的高流行率及固定情况
Am J Trop Med Hyg. 2009 Jul;81(1):19-22.
5
Evaluation of Plasmodium vivax genotyping markers for molecular monitoring in clinical trials.间日疟原虫基因分型标记物在临床试验中用于分子监测的评估。
J Infect Dis. 2009 Apr 1;199(7):1074-80. doi: 10.1086/597303.
6
A trial of combination antimalarial therapies in children from Papua New Guinea.在巴布亚新几内亚儿童中进行的联合抗疟疗法试验。
N Engl J Med. 2008 Dec 11;359(24):2545-57. doi: 10.1056/NEJMoa0804915. Epub 2008 Dec 8.
7
Plasmodium vivax resistance to chloroquine in Madagascar: clinical efficacy and polymorphisms in pvmdr1 and pvcrt-o genes.马达加斯加间日疟原虫对氯喹的耐药性:pvmdr1和pvcrt - o基因的临床疗效及多态性
Antimicrob Agents Chemother. 2008 Dec;52(12):4233-40. doi: 10.1128/AAC.00578-08. Epub 2008 Sep 22.
8
Molecular markers of in vivo Plasmodium vivax resistance to amodiaquine plus sulfadoxine-pyrimethamine: mutations in pvdhfr and pvmdr1.间日疟原虫体内对阿莫地喹加磺胺多辛-乙胺嘧啶耐药性的分子标志物:pvdhfr和pvmdr1中的突变
J Infect Dis. 2008 Aug 1;198(3):409-17. doi: 10.1086/589882.
9
Multidrug-resistant Plasmodium vivax associated with severe and fatal malaria: a prospective study in Papua, Indonesia.与严重和致命疟疾相关的多重耐药间日疟原虫:印度尼西亚巴布亚的一项前瞻性研究。
PLoS Med. 2008 Jun 17;5(6):e128. doi: 10.1371/journal.pmed.0050128.
10
Plasmodium vivax and mixed infections are associated with severe malaria in children: a prospective cohort study from Papua New Guinea.间日疟原虫及混合感染与儿童重症疟疾相关:来自巴布亚新几内亚的一项前瞻性队列研究
PLoS Med. 2008 Jun 17;5(6):e127. doi: 10.1371/journal.pmed.0050127.

基于中性和耐药相关标记物基因分型对治疗失败的疗效试验中抗间日疟原虫药物的特征描述。

Characterization of treatment failure in efficacy trials of drugs against Plasmodium vivax by genotyping neutral and drug resistance-associated markers.

机构信息

Vector Borne Diseases Unit, PNG Institute of Medical Research, Goroka, Papua New Guinea.

出版信息

Antimicrob Agents Chemother. 2011 Sep;55(9):4479-81. doi: 10.1128/AAC.01552-10. Epub 2011 Jun 27.

DOI:10.1128/AAC.01552-10
PMID:21709097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3165340/
Abstract

Plasmodium vivax intervention trials customarily report uncorrected treatment failure rates. Application of recrudescence-reinfection genotyping and drug resistance single-nucleotide polymorphism typing to a 4-arm comparative efficacy trial illustrated that molecular approaches can assist in understanding the relative contributions of true drug resistance (recurrent with same genotype) and new infections to treatment failure. The PCR-corrected adequate clinical and parasitologic response may constitute an informative secondary endpoint in future P. vivax drug trials.

摘要

间日疟原虫干预试验通常报告未经校正的治疗失败率。应用复发再感染基因分型和药物耐药性单核苷酸多态性分型对四臂比较疗效试验的研究表明,分子方法有助于了解真正的药物耐药性(与相同基因型复发)和新感染对治疗失败的相对贡献。PCR 校正后的充分临床和寄生虫学反应可能成为未来间日疟原虫药物试验的一个有用的次要终点。