AI Article Synopsis

  • The study examines perinatal outcomes in women with HIV and hepatitis B virus (HBV) co-infection, highlighting limited existing data on this topic.
  • It found that women with high HBV viral loads had significantly lower CD4 counts and their infants were more likely to be born with low birth weight compared to those with lower HBV viral loads or HIV alone.
  • The results suggest that managing HBV levels during pregnancy could reduce risks for infants and potentially decrease HIV transmission rates.

Article Abstract

Background: There is limited information on perinatal outcomes in HIV-hepatitis B virus (HBV) coinfection.

Methods: HIV Prevention Trials Network (HPTN) 046 was a randomized double-blind placebo-controlled trial of perinatal transmission that evaluated 6 months of infant nevirapine versus placebo among breast-fed infants. Women living with HIV and their infants enrolled in sub-Saharan Africa from 2007 to 2010; 78% received antiretroviral therapy (ART). Maternal samples were tested for hepatitis B surface antigen (HBsAg). High and low HBV viral load (VL) was defined as ≥106 IU/mL and <106 IU/mL. The association between HIV-HBV coinfection and maternal and infant outcomes was assessed using multivariate (MV) logistic and Cox regression.

Results: Among 2025 women, 88 (4.3%) had HBV. HIV-HBV women with high HBV VL had lower median CD4, versus HIV alone or HIV-HBV women with low HBV VL [320, 490 and 434 cells/mm3, respectively (P < 0.007)]. In MV analysis, adjusted for maternal CD4, age and maternal ART, infants born to women with high HBV VL were more likely to be low birth weight (LBW), versus HIV+/HBV- and low HBV VL women: [30% (3/10) vs. 10% (194/1953) vs. 6% (5/78), respectively, P = 0.03). High HBV VL was associated with HIV perinatal transmission [(hazard ratio 6.75 (95% confidence interval (CI): 1.86 - 24.50)]. There was no impact on infant mortality or maternal outcomes at 18 months.

Conclusions: In HIV-HBV women, high HBV viral loads increase the risk of LBW and potentially HIV perinatal transmission. Reduction of antepartum HBV viremia may have beneficial effects beyond the prevention of HBV perinatal transmission.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7855346PMC
http://dx.doi.org/10.1097/INF.0000000000002980DOI Listing

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