The effects of untreated and treated HIV infection on bone disease

Aoife G Cotter1, Patrick W G Mallon

  • 1aHIV Molecular Research Group, School of Medicine & Medical Science, University College Dublin bDepartment of Infectious Diseases, Mater Misericordiae University Hospital, Dublin, Ireland.

Insights

Low bone mineral density (BMD) is common in people with HIV. Earlier antiretroviral therapy (ART) initiation may help preserve BMD by mitigating immune and viral effects on bone metabolism.

Area of Science:

  • Bone metabolism and HIV research
  • Immunology and virology
  • Antiretroviral therapy (ART) effects

Background:

  • Low bone mineral density (BMD) is prevalent in individuals with HIV, linked to increased bone turnover and fracture risk.
  • This review examines the mechanisms behind low BMD in HIV, considering its relationship with HIV infection, immune status, and ART.
  • Understanding these factors is crucial for managing bone health in the HIV population.

Purpose of the Study:

  • To review the underlying mechanisms of low bone mineral density (BMD) in HIV.
  • To explore the relationship between low BMD, HIV infection, immune dysfunction, and antiretroviral therapy (ART).
  • To propose strategies for mitigating BMD loss in HIV patients.

Main Methods:

  • Literature review of studies on BMD in HIV patients.
  • Analysis of the impact of HIV viremia and immune status on BMD.
  • Examination of the role of antiretroviral therapy (ART) in bone metabolism.

Main Results:

  • Significant BMD reductions observed with decreasing HIV viral load during ART initiation.
  • Evidence suggests immune- or viral-mediated mechanisms contribute to low BMD pathogenesis.
  • ART initiation is associated with changes in BMD, highlighting the interplay between treatment and bone health.

Conclusions:

  • Bone metabolism is influenced by T cells and B cells, suggesting immune system involvement in BMD regulation.
  • Earlier ART initiation at higher CD4 T-cell counts may prevent BMD loss by reducing immune and viral disturbances.
  • Further research is needed to elucidate the complex interactions between HIV, the immune system, ART, and bone metabolism.
Abstract

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