Simplification from tenofovir disoproxil fumarate plus lamivudine or emtricitabine plus ritonavir-boosted protease inhibitor to ritonavir-boosted atazanavir plus lamivudine in virologically suppressed HIV-infected adults with osteopenia: a pilot study.
J Antimicrob Chemother
; 77(7): 1974-1979, 2022 06 29.
Article
en En
| MEDLINE
| ID: mdl-35512339
ABSTRACT
BACKGROUND:
Tenofovir disoproxil fumarate, particularly when given with a ritonavir-boosted PI, reduces bone mineral density (BMD) and increases bone turnover markers (BTMs). Ritonavir-boosted atazanavir plus lamivudine is a feasible simplified option. We evaluated whether switching from a triple ritonavir-boosted PI plus tenofovir disoproxil fumarate to a two-drug regimen of lamivudine plus ritonavir-boosted atazanavir would improve BMD.METHODS:
Single-arm pilot study. Virologically suppressed patients on tenofovir disoproxil fumarate plus lamivudine or emtricitabine plus ritonavir-boosted PI with low BMD, without previous resistance mutations and/or virological failure to study drugs were switched to 100/300â mg of ritonavir-boosted atazanavir plus 300â mg of lamivudine once daily. The primary endpoint was BMD change by DXA at Week 48.RESULTS:
There were 31 patients, 4 (13%) female, and median age was 40â years. Seven participants (22.5%) had osteoporosis. At 48â weeks, mean (SD) changes in spine and hip BMD were +0.01 (0.03) (Pâ=â0.0239) and +0.013 (0.03)â g/cm2 (Pâ=â0.0046), respectively. Mean (SD) T-score changes were +0.1 (0.23) (Pâ=â0.0089) and +0.25 (0.76) (Pâ=â0.0197), respectively. N-telopeptide and urine tenofovir disoproxil fumarate toxicity markers showed significant improvements. One participant withdrew from the study and two were lost to follow-up. There were no virological failures, or serious or grade 3-4 adverse events.CONCLUSIONS:
Switching from a tenofovir disoproxil fumarate plus ritonavir-boosted PI triple therapy to a lamivudine plus ritonavir-boosted atazanavir two-drug regimen in virologically suppressed HIV-infected adults with low BMD was safe, increased low BMD and reduced plasma markers of bone turnover and urine markers of tenofovir disoproxil fumarate toxicity over 48â weeks.
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Banco de datos:
MEDLINE
Asunto principal:
Enfermedades Óseas Metabólicas
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Infecciones por VIH
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Inhibidores de la Proteasa del VIH
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Fármacos Anti-VIH
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Sustitución de Medicamentos
Límite:
Adult
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Female
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Humans
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Male
Idioma:
En
Año:
2022
Tipo del documento:
Article