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被忽视疾病治疗的药物遗传学

Pharmacogenetics of the Treatment of Neglected Diseases.

作者信息

Cabral Tiffany Borges, de Oliveira Amanda Carvalho, Melo Gisely Cardoso de, Rodrigues-Soares Fernanda

机构信息

Department of Pathology, Genetics and Evolution, Federal University of Triângulo Mineiro, Uberaba 38025-180, Brazil.

Postgraduate Program in Tropical Medicine, Amazonas State University (PPGMT/UEA), Manaus 69040-000, Brazil.

出版信息

Genes (Basel). 2025 Jan 5;16(1):54. doi: 10.3390/genes16010054.

Abstract

BACKGROUND/OBJECTIVES: Pharmacogenetics (PGx) aims to identify individuals more likely to suffer from adverse reactions or therapeutic failure in drug treatments. However, despite most of the evidence in this area being from European populations, some diseases have also been neglected, such as HIV infection, malaria, and tuberculosis. With this review, we aim to emphasize which pharmacogenetic tests are ready to be implemented in treating neglected diseases that have some evidence and call attention to what is missing for these three diseases.

METHODS

A critical literature review on the PGx of HIV infection, malaria, and tuberculosis was performed.

RESULTS

There are three PGx guidelines for antiretroviral drugs used in HIV infection, one for malaria, and none for tuberculosis. Some evidence is already available, and some genes have already been identified, such as for primaquine treatment and for isoniazid. However, some barriers to the implementation are the lack of evidence due to the few studies on the diseases themselves and the admixture of the most affected populations, which must be considered, given the genetic differentiation of these populations.

CONCLUSIONS

PGx tests such as abacavir are already implemented in some places, and efavirenz/atazanavir is ready to implement if this medication is used. Other gene-drug associations were found but still do not present a clear recommendation. We call attention to the need to generate more evidence for testing treatments for other neglected diseases, such as malaria and tuberculosis, given their epidemiological importance and for the public health of less favored populations.

摘要

背景/目的:药物遗传学(PGx)旨在识别在药物治疗中更易出现不良反应或治疗失败的个体。然而,尽管该领域的大多数证据来自欧洲人群,但一些疾病也被忽视了,如艾滋病毒感染、疟疾和结核病。通过本综述,我们旨在强调哪些药物遗传学检测已准备好在治疗有一定证据的被忽视疾病中实施,并提请关注这三种疾病所缺失的内容。

方法

对艾滋病毒感染、疟疾和结核病的药物遗传学进行了批判性文献综述。

结果

有三项关于艾滋病毒感染中使用的抗逆转录病毒药物的药物遗传学指南,一项关于疟疾的指南,而关于结核病的指南则没有。已经有一些证据,并且已经鉴定出一些基因,如用于伯氨喹治疗的基因和用于异烟肼的基因。然而,实施方面的一些障碍是由于对这些疾病本身的研究较少以及受影响最严重人群的混合导致缺乏证据,鉴于这些人群的基因差异,这一点必须予以考虑。

结论

诸如阿巴卡韦等药物遗传学检测已在一些地方实施,如果使用依非韦伦/阿扎那韦这种药物,它也准备好实施。还发现了其他基因 - 药物关联,但仍未给出明确建议。鉴于疟疾和结核病等其他被忽视疾病在流行病学上的重要性以及对弱势群体公共卫生的影响,我们提请注意需要为这些疾病的治疗检测提供更多证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52c2/11764765/3fa75c81cc4e/genes-16-00054-g001.jpg

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