4.4 Article

Impact of HIV and antiretroviral drug exposure on lung growth and function over 2 years in an African Birth Cohort

期刊

AIDS
卷 34, 期 4, 页码 549-558

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0000000000002444

关键词

antiretroviral therapy; HIV; HIV exposure; infant; lung function

资金

  1. Wellcome Trust [204755/Z/16/Z, 098479/Z/12/Z, 203525/Z/16/Z]
  2. Bill and Melinda Gates Foundation [OPP1017641]
  3. Worldwide University Network Research Mobility Award
  4. Thrasher Foundation [9207]
  5. University of Cape Town
  6. Wellcome Trust [204755/Z/16/Z, 098479/Z/12/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

Objective: To assess the impact of HIV and antiretroviral exposure without infection on lung growth and function over the first 2 years of life. Design: Prospective observational study of an African birth cohort, Drakenstein Child Health Study. Method: Infants enrolled antenatally had lung function measured at 6 weeks, 1 and 2 years. HIV-infected women received antiretroviral therapy (ART) as per local guidelines. The association between HIV and antiretroviral exposure with lung function was assessed using mixed effects modelling. Results: Of 1143 infants born, two HIV-infected infants were excluded from analysis; 909 (80%) infants had lung function collected at 6 weeks [190 (21%) were HIV-exposed uninfected (HEU)]; 782 (69%) at 1 year and 741 (65%) at 2 years. At 6 weeks HEU infants had larger tidal volume compared with HIV-unexposed infants (1.13 ml, confidence interval: 0.02-2.23, P = 0.045). High maternal viral load was associated with a 17% lower expiratory flow over 2 years (0.17, confidence interval 0.00-0.34, P = 0.046). First-line ART initiated during pregnancy was associated with lower infant tidal volume at 6 weeks compared with those who initiated ART before pregnancy (-2.7 ml, -5.31 to -0.10, P = 0.042), and low maternal CD4(+) cell counts associated with lower infant tidal over 2 years (-11.1 ml, -18.58-3.58, P = 0.004). Conclusion: HIV exposure is associated with altered lung function in early life, with a vulnerable HEU subgroup based on maternal disease severity, immunological compromise and ART exposure. These data highlight the importance of ongoing surveillance of respiratory health in HEU children.

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