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Published on: May 9, 2025
Improvement of BMD after Switching from Lopinavir/R Plus Two Nucleos(T)ide Reverse Transcriptase Inhibitors to
M Crespo1,2, J Navarro1,2, M Martinez-Rebollar3
1a Hospital Universitari Vall d'Hebrón , Autonomous University of Barcelona , Barcelona , Spain.
Switching HIV patients from triple to dual therapy with lopinavir/ritonavir and lamivudine improved bone mineral density (BMD) over 48 weeks. Body fat distribution remained unchanged in both treatment groups.
Area of Science:
- HIV/AIDS research
- Pharmacology
- Bone metabolism
Background:
- Antiretroviral therapy (ART) can impact bone mineral density (BMD) and body fat distribution.
- Lopinavir/ritonavir combined with nucleoside reverse transcriptase inhibitors (NRTIs) is a common ART regimen.
- Optimizing ART regimens to mitigate long-term side effects is crucial for HIV management.
Purpose of the Study:
- To compare 48-week changes in BMD and body fat distribution.
- To evaluate outcomes in HIV patients continuing lopinavir/ritonavir plus two NRTIs versus switching to lopinavir/ritonavir plus lamivudine.
Main Methods:
- A randomized, open-label, multicenter substudy of an OLE study.
- Adult HIV-infected patients with viral suppression (<50 copies/mL for ≥6 months) were randomized.
- Dual-energy X-ray absorptiometry (DXA) assessed BMD and body fat at baseline and 48 weeks.
Main Results:
- Total BMD increased by 1.04% in the dual-therapy group (switching to lopinavir/ritonavir and lamivudine), with no significant change in the triple-therapy group.
- Discontinuing tenofovir-DF was associated with significant increases in total BMD and total hip BMD.
- No significant changes in body fat distribution were observed in either treatment group.
Conclusions:
- Switching to lopinavir/ritonavir plus lamivudine improved BMD in HIV patients on suppressive triple therapy.
- The findings suggest potential benefits of simplifying ART regimens for bone health.
- Further research may explore long-term effects and optimal ART strategies for bone health in HIV.
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