Cargando…
Hip Structural Parameters over 96 Weeks in HIV-Infected Adults Switching Treatment to Tenofovir-Emtricitabine or Abacavir-Lamivudine
BACKGROUND: Therapy with tenofovir is associated with lower bone mineral density (BMD), higher markers of bone turnover and increased fracture risk in HIV-infected adults. Bone structural parameters generated by hip structural analysis may represent a separate measure of bone strength, but have not...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983265/ https://www.ncbi.nlm.nih.gov/pubmed/24722774 http://dx.doi.org/10.1371/journal.pone.0094858 |
_version_ | 1782311294032936960 |
---|---|
author | Haskelberg, Hila Pocock, Nicholas Amin, Janaki Ebeling, Peter Robert Emery, Sean Carr, Andrew |
author_facet | Haskelberg, Hila Pocock, Nicholas Amin, Janaki Ebeling, Peter Robert Emery, Sean Carr, Andrew |
author_sort | Haskelberg, Hila |
collection | PubMed |
description | BACKGROUND: Therapy with tenofovir is associated with lower bone mineral density (BMD), higher markers of bone turnover and increased fracture risk in HIV-infected adults. Bone structural parameters generated by hip structural analysis may represent a separate measure of bone strength, but have not been assessed in HIV. METHODS: Dual-energy X-ray absorptiometry (DXA) scans from 254 HIV-infected adults randomised to simplify their existing dual nucleoside analogue reverse transcriptase inhibitor therapy to coformulated tenofovir-emtricitabine or abacavir-lamivudine were analysed using DXA-derived hip structural analysis software. Hip structural parameters included femoral strength index, section modulus, cross-sectional area, and cross-sectional moment of inertia. We used one-way ANOVA to test the relationship between nucleoside analogue type at baseline and structural parameters, multivariable analysis to assess baseline covariates associated with femoral strength index, and t-tests to compare mean change in structural parameters over 96 weeks between randomised groups. RESULTS: Participants taking tenofovir at baseline had lower section modulus (−107.3 mm(2), p = 0.001), lower cross-sectional area (−15.01 mm(3), p = 0.001), and lower cross-sectional moment of inertia (−2,036.8 mm(4), p = 0.007) than those receiving other nucleoside analogues. After adjustment for baseline risk factors, the association remained significant for section modulus (p = 0.008) and cross-sectional area (p = 0.002). Baseline covariates significantly associated with higher femoral strength index were higher spine T-score (p = 0.001), lower body fat mass (p<0.001), lower bone alkaline phosphatase (p = 0.025), and higher osteoprotegerin (p = 0.024). Hip structural parameters did not change significantly over 96 weeks and none was significantly affected by treatment simplification to tenofovir-emtricitabine or abacavir-lamivudine. CONCLUSION: In this population, tenofovir use was associated with reduced composite indices of bone strength as measured by hip structural analysis, but none of the structural parameters improved significantly over 96 weeks with tenofovir cessation. TRIAL REGISTRATION: ClinicalTrials.gov NCT00192634 |
format | Online Article Text |
id | pubmed-3983265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39832652014-04-15 Hip Structural Parameters over 96 Weeks in HIV-Infected Adults Switching Treatment to Tenofovir-Emtricitabine or Abacavir-Lamivudine Haskelberg, Hila Pocock, Nicholas Amin, Janaki Ebeling, Peter Robert Emery, Sean Carr, Andrew PLoS One Research Article BACKGROUND: Therapy with tenofovir is associated with lower bone mineral density (BMD), higher markers of bone turnover and increased fracture risk in HIV-infected adults. Bone structural parameters generated by hip structural analysis may represent a separate measure of bone strength, but have not been assessed in HIV. METHODS: Dual-energy X-ray absorptiometry (DXA) scans from 254 HIV-infected adults randomised to simplify their existing dual nucleoside analogue reverse transcriptase inhibitor therapy to coformulated tenofovir-emtricitabine or abacavir-lamivudine were analysed using DXA-derived hip structural analysis software. Hip structural parameters included femoral strength index, section modulus, cross-sectional area, and cross-sectional moment of inertia. We used one-way ANOVA to test the relationship between nucleoside analogue type at baseline and structural parameters, multivariable analysis to assess baseline covariates associated with femoral strength index, and t-tests to compare mean change in structural parameters over 96 weeks between randomised groups. RESULTS: Participants taking tenofovir at baseline had lower section modulus (−107.3 mm(2), p = 0.001), lower cross-sectional area (−15.01 mm(3), p = 0.001), and lower cross-sectional moment of inertia (−2,036.8 mm(4), p = 0.007) than those receiving other nucleoside analogues. After adjustment for baseline risk factors, the association remained significant for section modulus (p = 0.008) and cross-sectional area (p = 0.002). Baseline covariates significantly associated with higher femoral strength index were higher spine T-score (p = 0.001), lower body fat mass (p<0.001), lower bone alkaline phosphatase (p = 0.025), and higher osteoprotegerin (p = 0.024). Hip structural parameters did not change significantly over 96 weeks and none was significantly affected by treatment simplification to tenofovir-emtricitabine or abacavir-lamivudine. CONCLUSION: In this population, tenofovir use was associated with reduced composite indices of bone strength as measured by hip structural analysis, but none of the structural parameters improved significantly over 96 weeks with tenofovir cessation. TRIAL REGISTRATION: ClinicalTrials.gov NCT00192634 Public Library of Science 2014-04-10 /pmc/articles/PMC3983265/ /pubmed/24722774 http://dx.doi.org/10.1371/journal.pone.0094858 Text en © 2014 Haskelberg et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Haskelberg, Hila Pocock, Nicholas Amin, Janaki Ebeling, Peter Robert Emery, Sean Carr, Andrew Hip Structural Parameters over 96 Weeks in HIV-Infected Adults Switching Treatment to Tenofovir-Emtricitabine or Abacavir-Lamivudine |
title | Hip Structural Parameters over 96 Weeks in HIV-Infected Adults Switching Treatment to Tenofovir-Emtricitabine or Abacavir-Lamivudine |
title_full | Hip Structural Parameters over 96 Weeks in HIV-Infected Adults Switching Treatment to Tenofovir-Emtricitabine or Abacavir-Lamivudine |
title_fullStr | Hip Structural Parameters over 96 Weeks in HIV-Infected Adults Switching Treatment to Tenofovir-Emtricitabine or Abacavir-Lamivudine |
title_full_unstemmed | Hip Structural Parameters over 96 Weeks in HIV-Infected Adults Switching Treatment to Tenofovir-Emtricitabine or Abacavir-Lamivudine |
title_short | Hip Structural Parameters over 96 Weeks in HIV-Infected Adults Switching Treatment to Tenofovir-Emtricitabine or Abacavir-Lamivudine |
title_sort | hip structural parameters over 96 weeks in hiv-infected adults switching treatment to tenofovir-emtricitabine or abacavir-lamivudine |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983265/ https://www.ncbi.nlm.nih.gov/pubmed/24722774 http://dx.doi.org/10.1371/journal.pone.0094858 |
work_keys_str_mv | AT haskelberghila hipstructuralparametersover96weeksinhivinfectedadultsswitchingtreatmenttotenofoviremtricitabineorabacavirlamivudine AT pococknicholas hipstructuralparametersover96weeksinhivinfectedadultsswitchingtreatmenttotenofoviremtricitabineorabacavirlamivudine AT aminjanaki hipstructuralparametersover96weeksinhivinfectedadultsswitchingtreatmenttotenofoviremtricitabineorabacavirlamivudine AT ebelingpeterrobert hipstructuralparametersover96weeksinhivinfectedadultsswitchingtreatmenttotenofoviremtricitabineorabacavirlamivudine AT emerysean hipstructuralparametersover96weeksinhivinfectedadultsswitchingtreatmenttotenofoviremtricitabineorabacavirlamivudine AT carrandrew hipstructuralparametersover96weeksinhivinfectedadultsswitchingtreatmenttotenofoviremtricitabineorabacavirlamivudine AT hipstructuralparametersover96weeksinhivinfectedadultsswitchingtreatmenttotenofoviremtricitabineorabacavirlamivudine |