Pharmacogenomics in Infectious Diseases

A special issue of Genes (ISSN 2073-4425). This special issue belongs to the section "Human Genomics and Genetic Diseases".

Deadline for manuscript submissions: closed (20 July 2024) | Viewed by 1540

Special Issue Editor


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Guest Editor
Departamento de Patologia, Genética e Evolução, Instituto de Ciências Biológicas e Naturais, Universidade Federal do Triângulo Mineiro, Uberaba 35025-250, MG, Brazil
Interests: pharmacogenomics; population genetics

Special Issue Information

Dear Colleagues,

Pharmaceutical treatments for infectious diseases are often complicated to manage. In some cases, patients may suffer from adverse drug reactions (ADRs) and quit treatment, whereas in others patient’s may present therapeutic failure. These issues may be due to infectious agent resistance or host peculiarities. Pharmacogenomics is important to consider when host genetic variants may explain ADRs or therapeutic failure in drug treatments. In this Special Issue, we welcome manuscripts considering host genetic variants and infectious disease drug treatments.

Dr. Fernanda Rodrigues-Soares
Guest Editor

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Keywords

  • pharmacogenomics
  • pharmacogenetics
  • infectious diseases
  • malaria
  • tuberculosis
  • HIV infection

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Published Papers (1 paper)

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Review

16 pages, 700 KiB  
Review
Pharmacogenetics of the Treatment of Neglected Diseases
by Tiffany Borges Cabral, Amanda Carvalho de Oliveira, Gisely Cardoso de Melo and Fernanda Rodrigues-Soares
Genes 2025, 16(1), 54; https://doi.org/10.3390/genes16010054 - 5 Jan 2025
Viewed by 1196
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, [...] Read more.
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 CYP2D6 for primaquine treatment and NAT2 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. Full article
(This article belongs to the Special Issue Pharmacogenomics in Infectious Diseases)
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