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婴儿通过胎盘和母乳转移暴露于度鲁特韦:DOLPHIN-1 的群体药代动力学分析。

Infant Exposure to Dolutegravir Through Placental and Breast Milk Transfer: A Population Pharmacokinetic Analysis of DolPHIN-1.

机构信息

Department of Molecular & Clinical Pharmacology, University of Liverpool, Liverpool, United Kingdom.

Infectious Diseases Institute, Makerere University College of Health Sciences, Kampala, Uganda.

出版信息

Clin Infect Dis. 2021 Sep 7;73(5):e1200-e1207. doi: 10.1093/cid/ciaa1861.

Abstract

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.

摘要

背景

迅速降低人类免疫缺陷病毒(HIV)载量对于预防妊娠晚期诊断出的HIV 感染女性的围产期传播至关重要。我们研究了在 DolPHIN-1 参与者(NCT02245022)中,母体血浆、脐带、母乳和婴儿血浆样本中的多替拉韦群体药代动力学,这些参与者在妊娠晚期(28-36 周妊娠)时出现未经治疗的 HIV。

方法

来自乌干达和南非的孕妇按照 1:1 的比例随机分配接受每日多替拉韦(50mg/d)或依非韦伦为基础的治疗。在治疗开始后 14 天和分娩后 1-3 周内进行多替拉韦药代动力学采样(0-24 小时),并在分娩时采集配对的母体和脐带样本。母亲转为服用依非韦伦,在转换后 24、48 或 72 小时时,采集母亲和婴儿的血浆和母乳样本。使用非线性混合效应模型描述所有基质中的多替拉韦,并评估协变量。

结果

共纳入 28 名妇女和 22 名婴儿。母体多替拉韦由一个与胎儿和母乳室相连的 2 室模型描述。脐带和母乳与母体血浆的比值分别为 1.279(1.209-1.281)和 0.033(0.021-0.050)。婴儿多替拉韦由母乳至婴儿和婴儿消除速率常数来描述。未观察到协变量的影响。中位预测婴儿多替拉韦半衰期和高于此阈值的蛋白校正 90%抑制浓度(0.064mg/L)的中位时间分别为 37.9(范围,22.1-63.5)小时和 108.9(18.6-129.6)小时(4.5[0.8-5.4]天)(n=13)。

结论

母乳喂养对婴儿血浆暴露的贡献相对较小,但在母体多替拉韦停药后(产后 3-15 天),观察到一些母乳喂养婴儿需要额外的 4.5 天预防治疗,随着胎盘多替拉韦的清除,这种情况随着产后时间的推移而减弱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b14/8423479/ce02484c6c3b/ciaa1861f0001.jpg

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