应用于恰加斯病动物模型临床前研究的治疗方案:系统回顾和荟萃分析

Q2 Pharmacology, Toxicology and Pharmaceutics
F1000Research Pub Date : 2025-05-16 eCollection Date: 2024-01-01 DOI:10.12688/f1000research.150723.1
Laura Yesenia Machaca-Luque, Mayron Antonio Candia-Puma, Brychs Milagros Roque-Pumahuanca, Haruna Luz Barazorda-Ccahuana, Luis Daniel Goyzueta-Mamani, Alexsandro Sobreira Galdino, Ricardo Andrez Machado-de-Ávila, Rodolfo Cordeiro Cordeiro Giunchetti, Eduardo Antonio Ferraz Coelho, Miguel Angel Chavez-Fumagalli
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引用次数: 0

摘要

背景:恰加斯病是拉丁美洲一种被忽视的热带地方病,由于受感染个体的移徙而成为全球卫生问题。由于其流行病学的复杂性,由于难以获得适当的诊断和治疗不良,仍然需要寻找新的治疗方案。方法:在此背景下,我们对采用动物模型的临床前研究进行了系统回顾和荟萃分析,以验证乳糜泻治疗的进展。我们在PubMed数据库中检索了1990年至2023年间发表的CD治疗研究,并遵循PRISMA指南。结果:12篇论文符合纳入标准。研究结果表明,主要在2010年至2014年期间检测的15种治疗方案在实验性CD模型中显示出有效性,证明了寄生虫病的显著减少。双三唑DO870和VNI分别在急性期和慢性期有效。然而,在这些新兴疗法中,只有泊沙康唑和非昔硝唑进入了临床试验,作为乳糜泻的单一疗法,结果并不令人满意。结论:这项荟萃分析强调了存在有希望的新候选药物用于乳糜泻治疗,但大多数仍处于临床前阶段。那些进入临床试验的药物并没有显示出最佳结果,这强调了乳糜泻治疗面临的持续挑战。迫切需要学术界、制药行业、资助机构和政府机构之间的合作努力,以加速开发更有效的抗cd药物。inplasy注册:INPLASY202430101(25/03/2024)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment options applied to the preclinical studies using animal models for Chagas Disease: a systematic review and meta-analysis.

Background: Chagas disease (CD) is a neglected tropical disease endemic to Latin America, has emerged as a global health concern due to the migration of infected individuals. With its epidemiological complexity, by difficulty to obtain appropriate diagnoses and poor treatment, the search for novel therapeutic options remains.

Methods: In this context, we conducted a systematic review and meta-analysis of preclinical studies employing animal models to verify the progress in CD treatment. We searched the PubMed database for CD treatment studies published between 1990 and 2023, adhering to the PRISMA guidelines.

Results: Twelve papers met the inclusion criteria. The findings indicate that the fifteen treatment alternatives examined, mainly between 2010 and 2014, demonstrated efficacy in experimental CD models, evidenced by significant parasitemia reduction. Bis-triazole DO870 and VNI were effective in the acute and chronic phases, respectively. However, of these emerging therapies, only posaconazole and fexinidazole have progressed to clinical trials, yielding unsatisfactory outcomes as CD monotherapies.

Conclusions: This meta-analysis highlights the existence of promising new drug candidates for CD treatment, but most remain in the preclinical stages. Those that reached clinical trials did not demonstrate optimal results, underscoring the ongoing challenges in CD therapy. Collaborative efforts among the academic community, pharmaceutical industries, funding agencies, and government agencies are urgently needed to accelerate the development of more effective medications against CD.

Inplasy registration: INPLASY202430101 (25/03/2024).

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来源期刊
F1000Research
F1000Research Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.00
自引率
0.00%
发文量
1646
审稿时长
1 weeks
期刊介绍: F1000Research publishes articles and other research outputs reporting basic scientific, scholarly, translational and clinical research across the physical and life sciences, engineering, medicine, social sciences and humanities. F1000Research is a scholarly publication platform set up for the scientific, scholarly and medical research community; each article has at least one author who is a qualified researcher, scholar or clinician actively working in their speciality and who has made a key contribution to the article. Articles must be original (not duplications). All research is suitable irrespective of the perceived level of interest or novelty; we welcome confirmatory and negative results, as well as null studies. F1000Research publishes different type of research, including clinical trials, systematic reviews, software tools, method articles, and many others. Reviews and Opinion articles providing a balanced and comprehensive overview of the latest discoveries in a particular field, or presenting a personal perspective on recent developments, are also welcome. See the full list of article types we accept for more information.
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