Background
We investigate if switching from a ritonavir-boosted lopinavir (LPV/r)-based to an efavirenz-based antiretroviral therapy (ART) regimen is associated with beneficial bone development.
Methods
The CHANGES Bone Study follows HIV-infected children who participated in a non-inferiority randomized trial in Johannesburg, South Africa evaluating the safety and efficacy of pre-emptive switching to efavirenz (N=106) compared to remaining on LPV/r (N=113). HIV-uninfected children were also recruited. Whole body (WB) and lumbar spine bone mineral content (BMC) were assessed by dual-energy X-ray absorptiometry (DXA) at a cross-sectional visit. BMC Z-scores adjusted for sex, age, and height were generated. Physical activity (PA) and dietary intake were assessed. CD4 percentage and viral load were measured. We compared bone indices of HIV-infected to HIV-uninfected children and LPV/r to efavirenz by intent-to-treat.
Results
The 219 HIV-infected (52% male) and 219 HIV-uninfected (55% male) children were 6.4 and 7.0 years of age, respectively. Mean ART duration for HIV-infected children was 5.7 years. WB BMC Z-score was 0.17 lower for HIV-infected children compared to HIV-uninfected children after adjustment for PA, dietary vitamin D and calcium (p=0.03). WB BMC Z-score was 0.55 higher for HIV-infected children switched to efavirenz compared to those remaining on LPV/r after adjustment for PA, dietary vitamin D and calcium, CD4 percentage and viral load (p<0.0001).
Conclusion
South African HIV-infected children receiving ART have lower bone mass compared to HIV-uninfected controls. Accrued bone mass is positively associated with switching to efavirenz-based ART compared to remaining on LPV/r, providing additional rationale for limiting LPV/r exposure once viral suppression has been achieved.