Abstract

The long-term impact on bone health of lifelong HIV infection and prolonged ART in growing and developing children is not yet known. Measures of bone health in youth must be interpreted in the context of expected developmental and physiologic changes in bone mass, size, density and strength that occur from fetal through adult life. Low bone mineral density (BMD) appears to be common in perinatally HIV-infected youth, especially outside of high-income settings, but data are limited and interpretation complicated by the need for better pediatric norms. The potential negative effects of tenofovir on BMD and bone mass accrual are of particular concern as this drug may be used more widely in younger children. Emphasizing good nutrition, calcium and vitamin D sufficiency, weight-bearing exercise and avoidance of alcohol and smoking are effective and available approaches to maintain and improve bone health in all settings. More data are needed to inform therapies and monitoring for HIV-infected youth with proven bone fragility. While very limited data suggest lack of marked increase in fracture risk for youth with perinatal HIV infection, the looming concern for these children is that they may fail to attain their expected peak bone mass in early adulthood which could increase their risk for fractures and osteoporosis later in adulthood.

Highlights

  • More than 2 million children are infected with HIV. In most of the cases, HIV infection was acquired during pregnancy or intrapartum or through breastfeeding

  • Worldwide, more than 2 million children are infected with HIV

  • This article will focus on available data and remaining questions related to bone outcomes in perinatal HIV infection in the context of normal bone development, non-HIV factors that impact bone, and composition of antiretroviral therapy (ART) as well as an approach to detection, prevention and management of bone problems in this group

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Summary

Introduction

More than 2 million children are infected with HIV. In most of the cases, HIV infection was acquired during pregnancy or intrapartum or through breastfeeding. Factors that negatively impact bone development in the foetus, child and adolescent may contribute to a compromised PBM in the young adult, but the important clinical consequences may not manifest until decades later as increased risk of fractures and osteoporosis.

Results
Conclusion

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