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Antiretroviral Choice for HIV Impacts Antimalarial Exposure and Treatment Outcomes in Ugandan Children

Background. The optimal treatment of malaria in human immunodeficiency virus (HIV)–infected children requires consideration of critical drug–drug interactions in coinfected children, as these may significantly impact drug exposure and clinical outcomes. Methods. We conducted an intensive and sparse...

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Autores principales: Parikh, Sunil, Kajubi, Richard, Huang, Liusheng, Ssebuliba, Joshua, Kiconco, Sylvia, Gao, Qin, Li, Fangyong, Were, Moses, Kakuru, Abel, Achan, Jane, Mwebaza, Norah, Aweeka, Francesca T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946019/
https://www.ncbi.nlm.nih.gov/pubmed/27143666
http://dx.doi.org/10.1093/cid/ciw291
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author Parikh, Sunil
Kajubi, Richard
Huang, Liusheng
Ssebuliba, Joshua
Kiconco, Sylvia
Gao, Qin
Li, Fangyong
Were, Moses
Kakuru, Abel
Achan, Jane
Mwebaza, Norah
Aweeka, Francesca T.
author_facet Parikh, Sunil
Kajubi, Richard
Huang, Liusheng
Ssebuliba, Joshua
Kiconco, Sylvia
Gao, Qin
Li, Fangyong
Were, Moses
Kakuru, Abel
Achan, Jane
Mwebaza, Norah
Aweeka, Francesca T.
author_sort Parikh, Sunil
collection PubMed
description Background. The optimal treatment of malaria in human immunodeficiency virus (HIV)–infected children requires consideration of critical drug–drug interactions in coinfected children, as these may significantly impact drug exposure and clinical outcomes. Methods. We conducted an intensive and sparse pharmacokinetic/pharmacodynamic study in Uganda of the most widely adopted artemisinin-based combination therapy, artemether-lumefantrine. HIV-infected children on 3 different first-line antiretroviral therapy (ART) regimens were compared to HIV-uninfected children not on ART, all of whom required treatment for Plasmodium falciparum malaria. Pharmacokinetic sampling for artemether, dihydroartemisinin, and lumefantrine exposure was conducted through day 21, and associations between drug exposure and outcomes through day 42 were investigated. Results. One hundred forty-five and 225 children were included in the intensive and sparse pharmacokinetic analyses, respectively. Compared with no ART, efavirenz (EFV) reduced exposure to all antimalarial components by 2.1- to 3.4-fold; lopinavir/ritonavir (LPV/r) increased lumefantrine exposure by 2.1-fold; and nevirapine reduced artemether exposure only. Day 7 concentrations of lumefantrine were 10-fold lower in children on EFV vs LPV/r-based ART, changes that were associated with an approximate 4-fold higher odds of recurrent malaria by day 28 in those on EFV vs LPV/r-based ART. Conclusions. The choice of ART in children living in a malaria-endemic region has highly significant impacts on the pharmacokinetics and pharmacodynamics of artemether-lumefantrine treatment. EFV-based ART reduces all antimalarial components and is associated with the highest risk of recurrent malaria following treatment. For those on EFV, close clinical follow-up for recurrent malaria following artemether-lumefantrine treatment, along with the study of modified dosing regimens that provide higher exposure, is warranted.
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spelling pubmed-49460192016-07-19 Antiretroviral Choice for HIV Impacts Antimalarial Exposure and Treatment Outcomes in Ugandan Children Parikh, Sunil Kajubi, Richard Huang, Liusheng Ssebuliba, Joshua Kiconco, Sylvia Gao, Qin Li, Fangyong Were, Moses Kakuru, Abel Achan, Jane Mwebaza, Norah Aweeka, Francesca T. Clin Infect Dis HIV/AIDS Background. The optimal treatment of malaria in human immunodeficiency virus (HIV)–infected children requires consideration of critical drug–drug interactions in coinfected children, as these may significantly impact drug exposure and clinical outcomes. Methods. We conducted an intensive and sparse pharmacokinetic/pharmacodynamic study in Uganda of the most widely adopted artemisinin-based combination therapy, artemether-lumefantrine. HIV-infected children on 3 different first-line antiretroviral therapy (ART) regimens were compared to HIV-uninfected children not on ART, all of whom required treatment for Plasmodium falciparum malaria. Pharmacokinetic sampling for artemether, dihydroartemisinin, and lumefantrine exposure was conducted through day 21, and associations between drug exposure and outcomes through day 42 were investigated. Results. One hundred forty-five and 225 children were included in the intensive and sparse pharmacokinetic analyses, respectively. Compared with no ART, efavirenz (EFV) reduced exposure to all antimalarial components by 2.1- to 3.4-fold; lopinavir/ritonavir (LPV/r) increased lumefantrine exposure by 2.1-fold; and nevirapine reduced artemether exposure only. Day 7 concentrations of lumefantrine were 10-fold lower in children on EFV vs LPV/r-based ART, changes that were associated with an approximate 4-fold higher odds of recurrent malaria by day 28 in those on EFV vs LPV/r-based ART. Conclusions. The choice of ART in children living in a malaria-endemic region has highly significant impacts on the pharmacokinetics and pharmacodynamics of artemether-lumefantrine treatment. EFV-based ART reduces all antimalarial components and is associated with the highest risk of recurrent malaria following treatment. For those on EFV, close clinical follow-up for recurrent malaria following artemether-lumefantrine treatment, along with the study of modified dosing regimens that provide higher exposure, is warranted. Oxford University Press 2016-08-01 2016-05-03 /pmc/articles/PMC4946019/ /pubmed/27143666 http://dx.doi.org/10.1093/cid/ciw291 Text en © The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, contact journals.permissions@oup.com.
spellingShingle HIV/AIDS
Parikh, Sunil
Kajubi, Richard
Huang, Liusheng
Ssebuliba, Joshua
Kiconco, Sylvia
Gao, Qin
Li, Fangyong
Were, Moses
Kakuru, Abel
Achan, Jane
Mwebaza, Norah
Aweeka, Francesca T.
Antiretroviral Choice for HIV Impacts Antimalarial Exposure and Treatment Outcomes in Ugandan Children
title Antiretroviral Choice for HIV Impacts Antimalarial Exposure and Treatment Outcomes in Ugandan Children
title_full Antiretroviral Choice for HIV Impacts Antimalarial Exposure and Treatment Outcomes in Ugandan Children
title_fullStr Antiretroviral Choice for HIV Impacts Antimalarial Exposure and Treatment Outcomes in Ugandan Children
title_full_unstemmed Antiretroviral Choice for HIV Impacts Antimalarial Exposure and Treatment Outcomes in Ugandan Children
title_short Antiretroviral Choice for HIV Impacts Antimalarial Exposure and Treatment Outcomes in Ugandan Children
title_sort antiretroviral choice for hiv impacts antimalarial exposure and treatment outcomes in ugandan children
topic HIV/AIDS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946019/
https://www.ncbi.nlm.nih.gov/pubmed/27143666
http://dx.doi.org/10.1093/cid/ciw291
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