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Published on: September 26, 2011
Growth patterns among HIV-exposed infants receiving nevirapine prophylaxis in Pune, India
Malathi Ram1, Nikhil Gupte, Uma Nayak
1Johns Hopkins Bloomberg School of Public Health, Dept, of International Health/GDEC, Suite W5506, 615 N, Wolfe Street, Baltimore, MD 21205, USA. mram@jhsph.edu
Insights
Infant malnutrition is high in India. HIV-infected infants show significantly higher stunting and underweight by 12 months, highlighting the need for early growth monitoring.
Area of Science:
- Global Health
- Pediatrics
- Infectious Diseases
Background:
- India faces significant challenges with infant malnutrition.
- Limited research exists on growth patterns of HIV-exposed infants in India.
- The impact of HIV infection timing on infant growth in India requires further investigation.
Purpose of the Study:
- To compare growth patterns of HIV-infected and HIV-exposed but uninfected infants in India.
- To identify risk factors for stunting, underweight, and wasting in this population.
- To assess the impact of the Six Week Extended Nevirapine (SWEN) trial on infant growth.
Main Methods:
- Utilized data from the Six Week Extended Nevirapine (SWEN) trial.
- Compared growth patterns and timing of HIV infection at multiple time points (weeks and months).
- Employed random effects multivariable logistic regression to identify risk factors for malnutrition.
Main Results:
- Baseline stunting and underweight were similar, but diverged by 12 months, with higher rates in HIV-infected infants.
- Infants infected in utero experienced the poorest growth outcomes.
- Maternal CD4 count, infant HIV status, breastfeeding, birth weight, delivery mode, and gestational age were significant risk factors for stunting and underweight.
Conclusions:
- Early divergence in growth indices was observed between HIV-infected and uninfected infants.
- The timing of HIV infection and SWEN prophylaxis influenced growth outcomes.
- Implementing early growth monitoring for all HIV-exposed infants is a crucial, cost-effective strategy for improving health and survival.
Background:
India has among the highest rates of infant malnutrition. Few studies investigating the growth patterns of HIV-exposed infants in India or the impact of timing of HIV infection on growth in settings such as India exist.
Methods:
We used data from the Six Week Extended Nevirapine (SWEN) trial to compare the growth patterns of HIV-infected and HIV-exposed but uninfected infants accounting for timing of HIV infection, and to identify risk factors for stunting, underweight and wasting. Growth and timing of HIV infection were assessed at weeks 1, 2, 4, 6, 10, 14 weeks and 6, 9, 12 months of life. Random effects multivariable logistic regression method was used to assess factors associated with stunting, underweight and wasting.
Results:
Among 737 HIV-exposed infants, 93 (13%) were HIV-infected by 12 months of age. Among HIV-infected and uninfected infants, baseline prevalence of stunting (48% vs. 46%), underweight (27% vs. 26%) and wasting (7% vs. 11%) was similar (p>0.29), but by 12 months stunting and underweight, but not wasting, were significantly higher in HIV-infected infants (80% vs. 56%, 52% vs. 29%, p< 0.0001; 5% vs. 6%, p=0.65, respectively). These differences rapidly manifested within 4-6 weeks of birth. Infants infected in utero had the worst growth outcomes during the follow-up period. SWEN was associated with non-significant reductions in stunting and underweight among HIV-infected infants and significantly less wasting in HIV-uninfected infants. In multivariate analysis, maternal CD4 < 250, infant HIV status, less breastfeeding, low birth weight, non-vaginal delivery, and infant gestational age were significant risk factors for underweight and stunting.
Conclusion:
Baseline stunting and underweight was high in both HIV-infected and uninfected infants; growth indices diverged early and were impacted by timing of infection and SWEN prophylaxis. Early growth monitoring of all HIV-exposed infants is an important low-cost strategy for improving health and survival outcomes of these infants.
Trial Registration:
NCT00061321.
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