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Global perspectives on CYP2D6 associations with primaquine metabolism and Plasmodium vivax radical cure

Clinical trial and individual patient treatment outcomes have produced accumulating evidence that effective primaquine (PQ) treatment of Plasmodium vivax and P. ovale liver stage hypnozoites is associated with genetic variation in the human cytochrome P450 gene, CYP2D6. Successful PQ treatment of in...

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Autores principales: Olvany, Jasmine M., Williams, Scott M., Zimmerman, Peter A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705595/
https://www.ncbi.nlm.nih.gov/pubmed/36457706
http://dx.doi.org/10.3389/fphar.2022.752314
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author Olvany, Jasmine M.
Williams, Scott M.
Zimmerman, Peter A.
author_facet Olvany, Jasmine M.
Williams, Scott M.
Zimmerman, Peter A.
author_sort Olvany, Jasmine M.
collection PubMed
description Clinical trial and individual patient treatment outcomes have produced accumulating evidence that effective primaquine (PQ) treatment of Plasmodium vivax and P. ovale liver stage hypnozoites is associated with genetic variation in the human cytochrome P450 gene, CYP2D6. Successful PQ treatment of individual and population-wide infections by the Plasmodium species that generate these dormant liver stage forms is likely to be necessary to reach elimination of malaria caused by these parasites globally. Optimizing safe and effective PQ treatment will require coordination of efforts between the malaria and pharmacogenomics research communities.
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spelling pubmed-97055952022-11-30 Global perspectives on CYP2D6 associations with primaquine metabolism and Plasmodium vivax radical cure Olvany, Jasmine M. Williams, Scott M. Zimmerman, Peter A. Front Pharmacol Pharmacology Clinical trial and individual patient treatment outcomes have produced accumulating evidence that effective primaquine (PQ) treatment of Plasmodium vivax and P. ovale liver stage hypnozoites is associated with genetic variation in the human cytochrome P450 gene, CYP2D6. Successful PQ treatment of individual and population-wide infections by the Plasmodium species that generate these dormant liver stage forms is likely to be necessary to reach elimination of malaria caused by these parasites globally. Optimizing safe and effective PQ treatment will require coordination of efforts between the malaria and pharmacogenomics research communities. Frontiers Media S.A. 2022-11-15 /pmc/articles/PMC9705595/ /pubmed/36457706 http://dx.doi.org/10.3389/fphar.2022.752314 Text en Copyright © 2022 Olvany, Williams and Zimmerman. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Olvany, Jasmine M.
Williams, Scott M.
Zimmerman, Peter A.
Global perspectives on CYP2D6 associations with primaquine metabolism and Plasmodium vivax radical cure
title Global perspectives on CYP2D6 associations with primaquine metabolism and Plasmodium vivax radical cure
title_full Global perspectives on CYP2D6 associations with primaquine metabolism and Plasmodium vivax radical cure
title_fullStr Global perspectives on CYP2D6 associations with primaquine metabolism and Plasmodium vivax radical cure
title_full_unstemmed Global perspectives on CYP2D6 associations with primaquine metabolism and Plasmodium vivax radical cure
title_short Global perspectives on CYP2D6 associations with primaquine metabolism and Plasmodium vivax radical cure
title_sort global perspectives on cyp2d6 associations with primaquine metabolism and plasmodium vivax radical cure
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705595/
https://www.ncbi.nlm.nih.gov/pubmed/36457706
http://dx.doi.org/10.3389/fphar.2022.752314
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