The effects of maternal tenofovir disoproxil fumarate-emtricitabine-efavirenz treatment on the growth of breast feeding infants

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University of Pretoria

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Background: In South Africa, nearly a quarter of women of reproductive age live with HIV, resulting in a growing population of infants exposed to HIV and antiretroviral (ARV) medications both in utero and postpartum. This study aimed to explore critical concerns regarding the impact of ARV medication, particularly tenofovir disoproxil fumarate (TDF), on the growth of infants breastfed by women living with HIV (WLWHIV). Methodology: This study used previously obtained breast milk samples and growth data from the UmbiBaby study carried out in the Tshwane District. Breast milk samples were collected from 26 WLWHIV receiving TDF treatment and from a control group of 65 mothers not living with HIV at 14 weeks postpartum. Breast milk samples were analysed using LC-MS/MS to detect the presence of tenofovir (TFV) and its metabolites. Quantification was not performed due to sensitivity limitations. Macronutrient contents were assessed using a Miris Human Milk Analyser (HMA). Infant growth parameters were extracted from the REDCap database and assessed using a retrospective cohort design, focussing on mean anthropometry z-scores based on WHO standards and comparing HIV-exposed and uninfected (HEU) and HIV-unexposed and uninfected (HUU) infants from 6 weeks to 24 months of age through longitudinal analysis. Results: The optimised LC-MS/MS method detected TFV within a calibration range of 50–200 ng/mL (R² = 0.9945). Methodological challenges included matrix effects and limited instrument sensitivity, which restricted the lower limit of detection to 50 ng/mL for TFV. However, TFV-DP quantification was hindered by chemical instability and in-source fragmentation. The results confirmed that TFV concentrations in breast milk were well below paediatric therapeutic doses, supporting the safety of breastfeeding for WLWHIV on TDF therapy. Macronutrient analysis revealed breastfeeding rates were significantly lower among HEU infants from 6 months onward (p-values ranging from 0.0250 to 0.0065). Significantly higher protein content was detected in the breast milk of WLWHIV compared to controls at 6 weeks (p = 0.0074) and 18 months (p < 0.0001). Fat and energy content were significantly higher in the WLWHIV group at 12 months (fat: p = 0.0088; energy: p = 0.0015) and 18 months (fat: p = 0.0163; energy: p = 0.0099). Carbohydrate content remained stable between groups, with significant differences at 12 months (p = 0.0021) and 18 months (p = 0.0471). Infant growth analysis showed that HEU infants had lower weight-for-age z-scores at 6 weeks (p = 0.0223) and 14 weeks (p = 0.0294) compared to HUU infants. Length-for-age z-scores were significantly lower in HEU infants at 6 weeks (p = 0.0009), 14 weeks (p = 0.0006), 9 months (p = 0.0027), and 24 months (p = 0.0492). Weight-for-length (WFL) and body mass index-for-age (BMIZ) z-scores showed no significant differences between HEU and HIV-unexposed uninfected (HUU) infants throughout the study period. Conclusion: Although TFV and its metabolites were not quantified, the consistent macronutrient content of breast milk and mixed infant growth outcomes suggest that ARV exposure via breastfeeding may be limited. This warrants further investigation with more sensitive methods. The observed disparities in growth outcomes for HEU infants emphasize the need for early nutritional support and interventions. This study highlights the complex interplay between HIV exposure, TDF and breast feeding, macronutrient content, and infant growth. The findings will contribute to optimising ARV strategies for pregnant and lactating WLWHIV, ultimately fostering infant health. Keywords: Tenofovir Disoproxil Fumarate, Infant Growth, Breast feeding, HIV-Exposed Uninfected (HEU) Infants, Macronutrient Content, Antiretroviral Therapy, LC-MS/MS, Infant Growth Trajectories, ARV Drug Exposure, Nutritional Support

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Dissertation (MSc)--University of Pretoria, 2025.

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UCTD, Sustainable Development Goals (SDGs), Tenofovir disoproxil fumarate (TDF), Infant growth, Breast feeding, HIV-exposed uninfected (HEU) infants, Macronutrient content, Liquid chromatography-tandem mass spectrometry (LC MS/MS), Infant growth trajectories, Antiretroviral (ARV) drug exposure, Nutritional support

Sustainable Development Goals

SDG-03: Good health and well-being

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