Related Experiment Video
Updated: Jan 11, 2026

Determination of Reproductive Competence by Confirming Pubertal Onset and Performing a Fertility Assay in Mice and Rats
Published on: October 13, 2018
Brief Report: Is Gestational Exposure to HIV and Protease Inhibitors Associated With Timing of Pubertal Onset?
Lena Serghides1,2, Jessica Lee3, Denise L Jacobson3
1University Health Network, Toronto, Canada.
Insights
Gestational HIV exposure may advance pubertal onset in boys. Higher maternal viral load was linked to earlier puberty in HIV-exposed but uninfected boys by age 9.
Area of Science:
- Pediatric Endocrinology
- HIV/AIDS Research
- Public Health
Background:
- Limited research exists on how gestational HIV and antiretroviral exposure affects puberty in HIV-exposed but uninfected children (CHEU).
- Understanding pubertal development in CHEU is crucial for monitoring long-term health outcomes.
Purpose of the Study:
- To investigate the association between gestational HIV exposure and pubertal onset in CHEU.
- To explore the impact of maternal HIV viral load on pubertal timing in CHEU.
Main Methods:
- Compared pubertal onset at age 9 in CHEU and HIV-unexposed uninfected children (CHUU) using Tanner staging.
- Employed log-binomial regression to estimate relative risks (RRs) of pubertal onset.
- Assessed the influence of maternal protease inhibitor exposure, CD4 count, and viral load on pubertal onset in CHEU.
Main Results:
- Male CHEU showed a higher likelihood of pubertal onset by age 9 compared to male CHUU.
- No significant difference in pubertal onset was observed between female CHEU and CHUU.
- Higher maternal HIV viral load (>400 copies/mL) in CHEU was associated with a significantly greater likelihood of pubertal onset in males.
Conclusions:
- Gestational HIV exposure, particularly with higher maternal viral load, is linked to earlier pubertal onset in male CHEU.
- Further research is needed to confirm these findings and understand the underlying mechanisms.
Background:
Few studies have evaluated the influence of gestational HIV/antiretroviral exposure on pubertal onset in children who are HIV-exposed but uninfected (CHEU).
Methods:
CHEU in the Surveillance Monitoring for ART Toxicities study and children HIV-unexposed uninfected (CHUU) in the Bone Mineral Density in Childhood Study with Tanner staging at age 9 years were included. Pubertal onset was defined as Tanner stage ≥2 for each sex-specific puberty indicator. Log-binomial regression models were fit to estimate relative risks (RRs) of pubertal onset in CHEU vs. CHUU, adjusted for exact age and other covariates. Among CHEU, models were fit to assess the association of pubertal onset with maternal protease inhibitor exposure, CD4 count, and earliest HIV viral load (VL) during pregnancy.
Results:
In total, 227 CHEU (114 female, 113 male) and 344 CHUU (182 female, 162 male) were included. Among male CHEU, the adjusted likelihood of pubertal onset by age 9 years was 2.07 times higher [95% CI: 0.89 to 4.79] for genitalia and 3.55 times higher [95% CI: 0.92 to 13.81] for pubic hair than male CHUU. Pubertal onset was similar in female CHEU and CHUU. Among male CHEU, a maternal VL ≥400 copies/mL was associated with a greater likelihood of pubertal onset (adjusted RR: 12.6 [95% CI: 1.56 to 102] for genitalia and 9.85 [95% CI: 1.17 to 83] for pubic hair).
Conclusions:
Gestational HIV exposure and exposure to higher maternal HIV viral load were associated with greater likelihood of pubertal onset by age 9 years in male CHEU. Further confirmatory and mechanistic studies are warranted.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Excretion
Signs of Puberty
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Teratogenicity
Sexually Transmitted Infections
Pharmacokinetics in Pediatric Patients: Drug Distribution

