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Infant Exposure to Dolutegravir Through Placental and Breast Milk Transfer: A Population Pharmacokinetic Analysis of DolPHIN-1
BACKGROUND: Rapid reduction in human immunodeficiency virus (HIV) load is paramount to prevent peripartum transmission in women diagnosed late in pregnancy. We investigated dolutegravir population pharmacokinetics in maternal plasma, umbilical cord, breast milk, and infant plasma samples from DolPHI...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8423479/ https://www.ncbi.nlm.nih.gov/pubmed/33346335 http://dx.doi.org/10.1093/cid/ciaa1861 |
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author | Dickinson, Laura Walimbwa, Stephen Singh, Yashna Kaboggoza, Julian Kintu, Kenneth Sihlangu, Mary Coombs, Julie-Anne Malaba, Thokozile R Byamugisha, Josaphat Pertinez, Henry Amara, Alieu Gini, Joshua Else, Laura Heiberg, Christie Hodel, Eva Maria Reynolds, Helen Myer, Landon Waitt, Catriona Khoo, Saye Lamorde, Mohammed Orrell, Catherine |
author_facet | Dickinson, Laura Walimbwa, Stephen Singh, Yashna Kaboggoza, Julian Kintu, Kenneth Sihlangu, Mary Coombs, Julie-Anne Malaba, Thokozile R Byamugisha, Josaphat Pertinez, Henry Amara, Alieu Gini, Joshua Else, Laura Heiberg, Christie Hodel, Eva Maria Reynolds, Helen Myer, Landon Waitt, Catriona Khoo, Saye Lamorde, Mohammed Orrell, Catherine |
author_sort | Dickinson, Laura |
collection | PubMed |
description | BACKGROUND: Rapid reduction in human immunodeficiency virus (HIV) load is paramount to prevent peripartum transmission in women diagnosed late in pregnancy. We investigated dolutegravir population pharmacokinetics in maternal plasma, umbilical cord, breast milk, and infant plasma samples from DolPHIN-1 participants (NCT02245022) presenting with untreated HIV late in pregnancy (28–36 weeks gestation). METHODS: Pregnant women from Uganda and South Africa were randomized (1:1) to daily dolutegravir (50 mg/d) or efavirenz-based therapy. Dolutegravir pharmacokinetic sampling (0–24 hours) was undertaken 14 days after treatment initiation and within 1–3 weeks after delivery, with matched maternal and cord samples at delivery. Mothers were switched to efavirenz, and maternal and infant plasma and breast milk samples were obtained 24, 48, or 72 hours after the switch. Nonlinear mixed-effects modeling was used to describe dolutegravir in all matrices and to evaluate covariates. RESULTS: A total of 28 women and 22 infants were included. Maternal dolutegravir was described by a 2-compartment model linked to a fetal and breast milk compartment. Cord and breast milk to maternal plasma ratios were 1.279 (1.209–1.281) and 0.033 (0.021–0.050), respectively. Infant dolutegravir was described by breast milk–to–infant and infant elimination rate constants. No covariate effects were observed. The median predicted infant dolutegravir half-life and median time to protein-adjusted 90% inhibitory concentration (0.064 mg/L) for those above this threshold were 37.9 (range, 22.1–63.5) hours and 108.9 (18.6–129.6) hours (4.5 [0.8–5.4] days) (n = 13), respectively. CONCLUSIONS: Breastfeeding contributed relatively little to infant plasma exposure, but a median of 4.5 days of additional prophylaxis to some of the breastfed infants was observed after cessation of maternal dolutegravir (3–15 days postpartum), which waned with time postpartum as transplacental dolutegravir cleared. |
format | Online Article Text |
id | pubmed-8423479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84234792021-09-09 Infant Exposure to Dolutegravir Through Placental and Breast Milk Transfer: A Population Pharmacokinetic Analysis of DolPHIN-1 Dickinson, Laura Walimbwa, Stephen Singh, Yashna Kaboggoza, Julian Kintu, Kenneth Sihlangu, Mary Coombs, Julie-Anne Malaba, Thokozile R Byamugisha, Josaphat Pertinez, Henry Amara, Alieu Gini, Joshua Else, Laura Heiberg, Christie Hodel, Eva Maria Reynolds, Helen Myer, Landon Waitt, Catriona Khoo, Saye Lamorde, Mohammed Orrell, Catherine Clin Infect Dis Online Only Articles BACKGROUND: Rapid reduction in human immunodeficiency virus (HIV) load is paramount to prevent peripartum transmission in women diagnosed late in pregnancy. We investigated dolutegravir population pharmacokinetics in maternal plasma, umbilical cord, breast milk, and infant plasma samples from DolPHIN-1 participants (NCT02245022) presenting with untreated HIV late in pregnancy (28–36 weeks gestation). METHODS: Pregnant women from Uganda and South Africa were randomized (1:1) to daily dolutegravir (50 mg/d) or efavirenz-based therapy. Dolutegravir pharmacokinetic sampling (0–24 hours) was undertaken 14 days after treatment initiation and within 1–3 weeks after delivery, with matched maternal and cord samples at delivery. Mothers were switched to efavirenz, and maternal and infant plasma and breast milk samples were obtained 24, 48, or 72 hours after the switch. Nonlinear mixed-effects modeling was used to describe dolutegravir in all matrices and to evaluate covariates. RESULTS: A total of 28 women and 22 infants were included. Maternal dolutegravir was described by a 2-compartment model linked to a fetal and breast milk compartment. Cord and breast milk to maternal plasma ratios were 1.279 (1.209–1.281) and 0.033 (0.021–0.050), respectively. Infant dolutegravir was described by breast milk–to–infant and infant elimination rate constants. No covariate effects were observed. The median predicted infant dolutegravir half-life and median time to protein-adjusted 90% inhibitory concentration (0.064 mg/L) for those above this threshold were 37.9 (range, 22.1–63.5) hours and 108.9 (18.6–129.6) hours (4.5 [0.8–5.4] days) (n = 13), respectively. CONCLUSIONS: Breastfeeding contributed relatively little to infant plasma exposure, but a median of 4.5 days of additional prophylaxis to some of the breastfed infants was observed after cessation of maternal dolutegravir (3–15 days postpartum), which waned with time postpartum as transplacental dolutegravir cleared. Oxford University Press 2020-12-21 /pmc/articles/PMC8423479/ /pubmed/33346335 http://dx.doi.org/10.1093/cid/ciaa1861 Text en © The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Online Only Articles Dickinson, Laura Walimbwa, Stephen Singh, Yashna Kaboggoza, Julian Kintu, Kenneth Sihlangu, Mary Coombs, Julie-Anne Malaba, Thokozile R Byamugisha, Josaphat Pertinez, Henry Amara, Alieu Gini, Joshua Else, Laura Heiberg, Christie Hodel, Eva Maria Reynolds, Helen Myer, Landon Waitt, Catriona Khoo, Saye Lamorde, Mohammed Orrell, Catherine Infant Exposure to Dolutegravir Through Placental and Breast Milk Transfer: A Population Pharmacokinetic Analysis of DolPHIN-1 |
title | Infant Exposure to Dolutegravir Through Placental and Breast Milk Transfer: A Population Pharmacokinetic Analysis of DolPHIN-1 |
title_full | Infant Exposure to Dolutegravir Through Placental and Breast Milk Transfer: A Population Pharmacokinetic Analysis of DolPHIN-1 |
title_fullStr | Infant Exposure to Dolutegravir Through Placental and Breast Milk Transfer: A Population Pharmacokinetic Analysis of DolPHIN-1 |
title_full_unstemmed | Infant Exposure to Dolutegravir Through Placental and Breast Milk Transfer: A Population Pharmacokinetic Analysis of DolPHIN-1 |
title_short | Infant Exposure to Dolutegravir Through Placental and Breast Milk Transfer: A Population Pharmacokinetic Analysis of DolPHIN-1 |
title_sort | infant exposure to dolutegravir through placental and breast milk transfer: a population pharmacokinetic analysis of dolphin-1 |
topic | Online Only Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8423479/ https://www.ncbi.nlm.nih.gov/pubmed/33346335 http://dx.doi.org/10.1093/cid/ciaa1861 |
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