Bone turnover change after randomised switch from tenofovir disoproxil to tenofovir alafenamide fumarate in men with HIV
Amelia E.B. Moore, James E. Burns, Deirdre Sally, Ana Milinkovic, Georgios Krokos, Joemon John, Christopher Rookyard, Alessandro Borca, Erica R.M. Pool, Anna Tostevin, Alyss Harman, Dwight S. Dulnoan, Musib Siddique, Richard Gilson, Alejandro Arenas-Pinto, Gary J.R. Cook, John Saunders, David Dunn, Glen M. Blake, Sarah L. Pett- Infectious Diseases
- Immunology
- Immunology and Allergy
Objective:
Bone loss in people with HIV (PWH) is poorly understood. Switching tenofovir disoproxil fumarate (TDF) to tenofovir alafenamide (TAF) has yielded bone mineral density (BMD) increases. PETRAM (NCT#:03405012) investigated whether BMD and bone turnover changes correlate.
Design:
Open-label, randomized controlled trial.
Setting:
Single-site, outpatient, secondary care.
Participants:
Nonosteoporotic, virologically suppressed, cis-male PWH taking TDF/emtricitabine (FTC)/rilpivirine (RPV) for more than 24 weeks.
Intervention:
Continuing TDF/FTC/RPV versus switching to TAF/FTC/RPV (1 : 1 randomization).
Main outcome measures:
:[18F]NaF-PET/CT for bone turnover (standardized uptake values, SUVmean) and dual-energy x-ray absorptiometry for lumbar spine and total hip BMD.
Results:
Thirty-two men, median age 51 years, 76% white, median duration TDF/FTC/RPV 49 months, were randomized between 31 August 2018 and 09 March 2020. Sixteen TAF:11 TDF were analyzed. Baseline-final scan range was 23–103 (median 55) weeks. LS-SUVmean decreased for both groups (TAF -7.9% [95% confidence interval -14.4, -1.5], TDF -5.3% [-12.1,1.5],
Conclusion:
Contrary to our hypothesis, lumbar spine and total hip regional bone formation (SUVmean) and BMD did not differ postswitch to TAF. However, improved LS-BMD and CTX echo other TAF-switch studies. The lack of difference in SUVmean may be due to inadequate power.