Those receiving tenofovir/emtricitabine (TDF-FTC) had greater bone loss compared with abacavir/lamivudine (ABC-3TC) in a randomized simplification trial (STEAL study). Previous studies associated increased bone turnover and bone loss with initiation of antiretroviral treatment, however it is unclear whether change in bone mineral density (BMD) was a result of specific drugs, from immune reconstitution or from suppression of HIV replication. This analysis determined predictors of BMD change in the hip and spine by dual-energy x-ray absorptiometry in virologically suppressed participants through week 96.
Bone turnover markers (BTMs) tested were: formation [bone alkaline phosphatase, procollagen type 1 N-terminal propeptide (P1NP)]; resorption (C-terminal cross-linking telopeptide of type 1 collagen [CTx]); and bone cytokine-signalling (osteoprotegerin, RANK ligand). Independent predictors of BMD change were determined using forward, stepwise, linear regression. BTM changes and fracture risk (FRAX®) at week 96 were compared by t-test. Baseline characteristics (n = 301) were: 98% male, mean age 45 years, current protease-inhibitor (PI) 23%, tenofovir/abacavir-naïve 52%. Independent baseline predictors of greater hip and spine bone loss were TDF-FTC randomisation (p≤0.013), lower fat mass (p-trend≤0.009), lower P1NP (p = 0.015), and higher hip T score/spine BMD (p-trend≤0.006). Baseline PI use was associated with greater spine bone loss (p = 0.004). TDF-FTC increased P1NP and CTx through Wk96 (p<0.01). Early changes in BTM did not predict bone loss at week 96. No significant between-group difference was found in fracture risk.
Citation: Haskelberg H, Hoy JF, Amin J, Ebeling PR, Emery S, Carr A, et al. (2012) Changes in Bone Turnover and Bone Loss in HIV-Infected Patients Changing Treatment to Tenofovir-Emtricitabine or Abacavir-Lamivudine. PLoS ONE 7(6): e38377. https://doi.org/10.1371/journal.pone.0038377
Editor: Landon Myer, University of Cape Town, South Africa
Received: January 18, 2012; Accepted: May 4, 2012; Published: June 15, 2012
Copyright: © 2012 Haskelberg et al. 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 credited.
Funding: This work was supported by The Kirby Institute (formerly the National Centre in HIV Epidemiology and Clinical Research) funded by the Australian Government Department of Health and Ageing. The views expressed in this publication do not necessarily represent the position of the Australian Government. The Kirby Institute is affiliated with the Faculty of Medicine, University of New South Wales. Partial funding for the biomarker analysis was provided by GSK/ViiV Healthcare. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. No additional external funding received for this study.
Competing interests: Co-author Sean Emery is a PLoS ONE Editorial Board member, Hila Haskelberg declares no conflict of interest. Jennifer Hoy’s institution has received research funding from GlaxoSmithKline/ViiV Healthcare, Gilead Sciences and Merck; travel sponsorship from Gilead Sciences, Janssen-Cilag, and Merck; and has served on advisory boards for Bristol-Myers Squibb, Gilead Sciences, GlaxoSmithKline/ViiV Healthcare, Janssen-Cilag, Merck and Roche. Janaki Amin declares no conflict of interest. Peter Ebeling’s institution has received research funding from Merck; consultancy fees from Gilead Sciences and GlaxoSmithKline/ViiV Healthcare; and he has served on an advisory board for Merck. Sean Emery has either served on advisory boards; received travel grants, consultancy payments or honoraria from Abbott, BMS, Merck, Gilead, GSK, Tibotec, Viiv Healthcare, and Pfizer. Andrew Carr has received research funding from GlaxoSmithKline/ViiV Healthcare, and Merck; consultancy fees from Bristol-Myers Squibb, Gilead Sciences, GlaxoSmithKline/ViiV Healthcare, Merck and Roche; lecture and travel sponsorships from Abbott, Boehringer- Ingelheim, Bristol-Myers Squibb, Gilead Sciences, GlaxoSmithKline/ViiV Healthcare, and Merck; and has served on advisory boards for Abbott, Bristol-Myers Squibb, Gilead Sciences, GlaxoSmithKline/ViiV Healthcare, Merck and Roche. This does not alter our adherence to all the PLoS ONE policies on sharing data and materials. Partial funding for the biomarker analysis was provided by GSK/ViiV Healthcare. This does not alter our adherence to all the PLoS ONE policies on sharing data and materials. In the STEAL main study, subjects were randomised to receive either of the following study drugs in combination with the remainder of their existing ART (having ceased the NRTI component): KivexaTM: ABC 600 mg+3 TC 300 mg FDC once daily TruvadaTM: FTC 200 mg+TDF 300 mg FDC once daily There are no other relevant declarations relating to employment, consultancy, patents, products in development or marketed products.
Highly active antiretroviral therapy (HAART) significantly improves survival and quality of life for individuals with human immunodeficiency virus (HIV) infection. However, clinical management challenges now include several disorders associated with aging, including higher prevalence of low bone mineral density (BMD)  and higher rates of fractures  than in adults without HIV. Prospective studies, mostly small and/or non-randomized, have generally found that ART initiation reduced BMD by 1% to 5% over 1 to 2 years (reviewed in ) although this initial short-term bone loss may not be ongoing . These rates of bone loss appear greater than those expected in healthy men, being more similar to those in post-menopausal women . Therapy with tenofovir (TDF) has been associated with greater reductions in BMD than with stavudine or abacavir (ABC) , , . Bone metabolism can be assessed by measuring serum bone turnover markers (BTMs), comprising proteins synthesized during bone formation, bone matrix proteins, and bone collagen degradation products released during bone resorption. High levels of BTMs have been found to predict fractures independently of BMD in post-menopausal women  and elderly men . Furthermore, as BTMs can provide a more dynamic estimate of bone metabolism in shorter timescales than BMD, these markers have been suggested as additional tools for more rapid assessment of bone disease . Interleukin-1 (IL-1), IL-6, and tumour necrosis factor-alpha (TNF-α) can all increase bone resorption , and their circulating levels predict changes in BMD in HIV-uninfected adults . Despite undetectable HIV viral load on ART, HIV-infected individuals have significantly higher levels of IL-6 compared with the general population .
BTMs have been found to be elevated in ART-treated compared with untreated patients in some cross-sectional studies , , . In a trial of ART-naive patients, those randomized to TDF-emtricitabine (FTC) had greater bone loss and greater BTM increases over 24 weeks than those randomised to ABC-lamivudine (3TC) . Other studies have shown that early increases in bone resorption were associated with BMD decreases and were followed by increased bone formation in ART-naïve adults, but it is not possible from these data to determine whether the BMD and BTM changes were a result of specific drugs, from immune reconstitution or from suppression of HIV replication , .
In the STEAL study, virologically suppressed patients randomized to simplify dual nucleoside analogue reverse transcriptase inhibitor (NRTI) therapy to coformulated TDF-FTC had greater bone loss over 96 weeks than those randomised to co-formulated ABC-3TC . This analysis aimed to explore STEAL bone outcomes in more detail and to determine predictors of BMD change. We hypothesized that some patients might be at greater risk of TDF-related BMD loss over 96 weeks and that this greater loss might be predicted by either baseline or on-study BTM levels.
STEAL was an open-label, prospective, randomized, non-inferiority study that compared simplification of current NRTIs to fixed-dose combination TDF-FTC or ABC-3TC over 96 weeks in 357 adults with plasma HIV viral load <50 copies/ml . The protocol for this trial and supporting CONSORT checklist are available as supporting information; see Protocol S1, Protocol S2 and Checklist S1.
The study was approved by each site’s Human Research and Ethics Committee (30 sites) and registered at Clinicaltrials.gov (NCT00192634). Each participant signed a written informed consent before enrolment.
Bone Mineral Density and Laboratory Markers
Dual-energy X-ray absorptiometry (DXA) of the lumbar spine and right hip were performed for each participant at the same imaging facility on the same bone densitometer, at baseline, week 48, and week 96, using a standardized protocol. BMD scans were not centrally analysed. DXA instruments varied between sites (GE-Lunar in 72% of sites); randomization was stratified by site, and therefore by model of DXA scanner.
Plasma and serum samples were collected at baseline and at weeks 12, 24, 48, 72 and 96 (following a 10-hour overnight fast, except at week 12) and stored at –70°C. Markers of bone resorption (C-terminal cross-linking telopeptide of type 1 collagen, [βCTX]; bone formation (procollagen type 1 N-terminal propeptide [P1NP]; bone-specific alkaline phosphatase,[BALP]) and regulators of bone turnover (osteoprotegerin [OPG] and receptor activator of nuclear factor kappa ligand [RANKL]) were evaluated. βCTX and P1NP were assayed by an electrochemiluminescence immunoassay (E170 immunoassay analyzer; Roche, Mannheim, Germany; reference ranges βCTX 170–600 ng/L, P1NP 16.3–78.2 ug/L). BALP, OPG and RANKL were assayed by Immunoenzymetric Assay (Manual with Plate Reader; Immunodiagnostic Systems, Boldon, United Kingdom; reference ranges BALP 8–21.3 ug/L, OPG <30 pmol/L, RANKL <100 pmol/L). The following were assessed at baseline only: Interleukin-6 by ELISA R&D Systems Human IL-6 (reference range 0.447–9.96 pg/ml); oestradiol by electrochemiluminescence (E170 immunoassay analyzer; Roche, reference range 50–200 pmol/L); free testosterone using total testosterone and sex hormone-binding globulin (Vermeulen formula ); and 25-hydroxy vitamin D by competitive chemiluminescence (Liasion; DiaSorin, Inc., Stillwater, MN, USA).
BTMs were batch-tested after study completion in one laboratory. Coefficients of variation were within accepted standard limits. The 10-year risks of osteoporotic and hip fractures were estimated using the FRAX® UK algorithm of the World Health Organization (WHO) . The proportion of participants above the threshold recommended for intervention with antiresorptive therapy was determined according to the US National Osteoporosis Foundation (NOF) guidelines . For the analysis of clinically relevant low BMD, low BMD was defined as T-score <−1 in accordance with WHO diagnostic thresholds .
Statistical analysis was conducted on the per protocol (PP) population, comprising all participants with BMD data and on randomized therapy at each time point. A PP approach was used to explore biological mechanisms of BMD change in response to study drug exposure. A pre-defined secondary analysis of this substudy was performed on the subpopulation that was not receiving ABC or TDF at study entry (“TDF/ABC-naïve”). Randomization was stratified by baseline NRTI use (TDF without ABC, ABC without TDF, or other), current protease inhibitor use, and study site. Absolute change in BMD at the lumbar spine and hip was the primary outcome of interest. Percent change was summarised as a secondary outcome.
The associations between baseline covariates (including demographic, HIV-related factors, ART, body composition, BTMs, bone remodelling regulators, sex hormones, vitamin D and IL-6; Table 1) and changes in BTMs from baseline to week 12, and absolute changes in hip and lumbar spine BMD to week 96 were analysed using linear regression. Three patients, all on TDF-FTC, started anti-resorptive therapy after week 48 and were included in the analysis. However, data on use of alcohol, glucocorticoids, vitamin D and calcium supplementation that can affect BMD were not collected. Multivariable models were built using forward, stepwise methods. Predictors that achieved a p-value <0.08 in univariate analysis (more conservative than 0.1) were assessed for inclusion in the multivariable model. Randomized groups were compared for changes in BTMs and FRAX® results by t-test at 48 weeks (BTMs only) and 96 weeks. Interaction between baseline exposure to TDF or ABC and randomized arm in predicting BTMs was tested using linear regression for the interaction term. Contingency-table and chi-square tests were used for analysis of proportions warranting antiresorptive-therapy (US NOF guidelines) and for incidence of low BMD. Sensitivity analysis was conducted for FRAX® results for participants who were at ≥40 years of age at baseline and for proportions warranting antiresorptive therapy (US NOF guidelines) for participants who are at ≥50 years of age at baseline. Pearson’s correlation was used to assess associations between changes in BTMs across the entire study population.
Statistical significance was defined as a 2-sided α of 0.05. All analyses of the main BMD and BTM outcomes were determined a priori and were hypothesis driven. No adjustment was made for multiple comparisons. Statistical analyses were performed with STATA, version 10.1 (Statacorp).
Of 357 participants enrolled in the parent study, 18 discontinued ABC-3TC and 16 discontinued TDF-FTC by week 96. An additional 22 participants (14 on ABC-3TC and 8 on TDF-FTC) did not have data for hip and spine BMD change from baseline to week 96. Therefore, the analysed per-protocol population comprised the remaining 301 participants (84% of main study population). Baseline characteristics of the population analysed were similar to main study  and well balanced between arms (Tables 1, 2).
Bone Mineral Density Change from Baseline
At week 96, the absolute change from baseline in hip BMD in the ABC-3TC group was 0.004 g/cm2 versus −0.007 g/cm2 in the TDF-FTC group (treatment difference 0.01 g/cm2 (95% confidence interval [CI] 0.003 to 0.018; p = 0.006). For lumbar spine, the absolute BMD change over 96 weeks in ABC-3TC group was 0.008 g/cm2 and −0.005 g/cm2 in the TDF-FTC group (treatment difference 0.01 g/cm2 (95% CI 0.002 to 0.024; p = 0.016). BMD changes in the ‘TDF/ABC-naïve’ subpopulation, were of similar magnitude (Table 2, Figure 1).
The right hand side of each graph shows the mean percent change in BMD at weeks 48 and 96. Note. p values from t-test comparing mean change from baseline to study week of interest in randomized arms. Error bars represent 1 standard deviation from the mean.Abbreviations: ABC/3TC, abacavir/lamivudine; TDF/FTC, tenofovir/emtricitabine.
Baseline Predictors of Change in Bone Mineral Density
Baseline covariates significantly associated with greater decline in hip BMD over 96 weeks in multivariable analysis were TDF-FTC randomisation (p = 0.001), lower fat mass (p trend = 0.009), lower P1NP (p = 0.015), and higher hip T-score (p trend = 0.006). Baseline predictors of greater decline in spine BMD were TDF-FTC randomisation (p = 0.013), lower fat mass (p trend = 0.005), protease inhibitor use (p = 0.004), and higher spine BMD (p = 0.001; Table 3).
Bone Turnover Markers
Significant differences in absolute changes in bone resorption and formation markers were seen after baseline between treatment groups. In the PP population, βCTx (bone resorption marker) increased significantly at week 12 in TDF-FTC compared to ABC-3TC arm (treatment difference 71.8 ng/L (95% CI 40.2 to 103.4; p<0.001)) and then remained stable through week 96. Similarly, increases in bone formation markers were greater with TDF-FTC than with ABC-3TC arm; P1NP was increased at week 12 (difference 8.79 µg/L [95% CI 5.48 to 12.10; p<0.001]) and remained stable thereafter. Another formation marker, BALP, was significantly different from week 24 onwards with greater increases with TDF-FTC than with ABC-3TC (difference 2.83 µg/L [95% CI 0.59 to 5.07; p = 0.014]) (Table 3, Figure 2). There was no significant, between-group difference in OPG or RANKL. Similar results were found in the ABC/TDF-naive subpopulation (data not shown). Changes in the bone resorption marker, βCTx, were correlated at all time points with changes in P1NP, a formation marker (r>0.30, p<0.001). Changes in BALP were correlated with changes in βCTx from week 24 onwards (r>0.15, p<0.014) except at week 48.
Note. Error bars represent 1 standard deviation from the mean (a) BALP, bone-specific alkaline phosphatase; (b) P1NP, procollagen type 1 N-terminal propeptide; (c) βCTx, C-terminal cross-linking telopeptide of type 1 collagen; (d) OPG, osteoprotegerin; ABC/3TC, abacavir/lamivudine; TDF/FTC, tenofovir/emtricitabine. There was no significant between-group difference at any time point for RANK.
There was no difference in FRAX® scores at 96 weeks either within each group or between groups. The FRAX® scores at week 96 for ten-year fracture risk for major osteoporotic fracture were: 3% for both ABC-3TC and TDF-FTC; hip fracture 0.4% with ABC-3TC vs. 0.5% with TDF-FTC in the PP population. There was no significant difference in the proportion (0.6% in ABC-3TC vs. 2.5% in TDF-FTC) of participants who met the NOF guidelines criteria for treatment by week 96. Similarly, there was no significant between-group difference in the incidence of participants who developed low hip BMD (T score ≤−1; 3.8% in ABC-3TC vs. 8.7% in TDF-FTC) or low spine BMD (3.8% in ABC-3TC vs. 7.4% in TDF-FTC) by week 96.
Small, yet significant differences between TDF-FTC and ABC-3TC in changes in absolute BMD values were found in our study, with greater bone loss in the TDF-FTC group over 96 weeks. Independent predictors for bone loss at both the hip and lumbar spine included TDF-FTC randomisation and lower baseline fat mass. Further, lower serum P1NP (bone formation marker) predicted greater hip bone loss, while protease inhibitor use at baseline predicted greater spine bone loss. BTMs significantly increased from week 12 with TDF-FTC, but their early changes (at week 12) did not predict subsequent bone loss. The clinical relevance of these changes is unknown.
Both the ASSERT study and ACTG 5224s, in ART-naive adults, found similar results over 48 weeks, showing greater increases in bone turnover  and decrease in BMD ,  in participants randomised to TDF-FTC compared with ABC-3TC. The greater BMD loss observed in ASSERT compared with our study may in part be due to different populations (ASSERT participants were younger, ART-naïve, more immunodeficient and more ethnically diverse).
The association found between protease inhibitor use and spine bone loss confirms findings by other investigators , . The spine comprises mainly trabecular bone, which is affected earlier than cortical bone (femoral neck) by high bone turnover . Protease inhibitors can reduce calcium deposition and alkaline phosphatase expression in osteoblasts , both markers of osteoblast differentiation. This effect may explain why PINP, a bone formation marker primarily expressed during osteoblast proliferation, was more sensitive in detecting TDF-FTC effects on bone loss. We showed PINP increased with TDF-FTC treatment, while BAP did not, and lower PINP levels predicted greater bone loss from the hip, but not the spine. The mechanisms underlying the effect of TDF on increasing bone loss have not been clearly established, although recent in vitro studies suggest TDF may alter gene expression in both osteoblasts and osteoclasts , . Furthermore, in similar settings without viraemia, a pre-exposure prophylaxis study found that initiation of TDF is also associated with bone loss, though bone turnover was not reported .
Higher baseline hip T-score and spine BMD predicted greater bone loss from the hip and spine, respectively in our study, an observation reported previously in the setting of allogeneic bone marrow transplantation . This finding provides reassurance that patients with low BMD are not particularly at risk of greater bone loss when receiving TDF. The findings regarding the effect of lower fat mass on bone loss are supported by similar evidence in the general population, suggesting a link between body composition and bone density and the protective role of obesity on bone . Other studies in HIV-infected adults have reported that low weight and BMI were associated with low BMD , , but we did not observe this association.
BTM levels increase following ART initiation , . One study found reductions in bone formation with increased resorption, which increased with more advanced untreated HIV infection, suggesting “uncoupling” of the usually well regulated processes of bone resorption and formation . After ART initiation, a “recoupling” of bone formation and resorption appears to occur, albeit with higher levels of bone turnover . It is not clear whether the early changes in BTMs after ART initiation reflect the effects of specific ART drugs, HIV suppression or immune reconstitution. Our study is the first to report BTM changes with ART switching in stable, virologically suppressed individuals.
We also evaluated whether baseline BTM levels and early BTM changes can predict BMD change with ART. Changes in markers to week 12 were not associated with BMD decrease at week 96. Only lower baseline levels of one bone formation marker (P1NP) predicted greater bone loss at the hip. BTMs were significantly increased in the TDF-FTC arm compared with ABC-3TC, as seen in the ASSERT study . These changes occurred early in the study (week 12) and bone turnover remained significantly higher in those randomized to TDF-FTC compared with ABC-3TC through 96 weeks. This is in contrast to the ASSERT study findings of similar bone resorption marker levels from week 48 onwards. Both studies show that formation and resorption remained coupled during study follow-up.
Although we could not assess fracture rates in this study, we explored other clinical implications by evaluating the 10-year fracture risk using the FRAX® algorithm and the incidence of participants above the FRAX threshold recommended for antiresorptive therapy according to NOF guidelines. No significant difference was found between TDF-FTC and ABC-3TC, even in analyses restricted to the older patients for which FRAX and NOF guidelines were designed, implying limited clinical significance. It is likely, however, that in addition to the small changes in BMD, the study was underpowered to detect significant risk differences between the groups. In addition, the FRAX equation requires additional clinical data not collected in STEAL (prior personal history of fracture, prior rheumatoid arthritis, family history of hip fracture, alcohol use). Therefore, the fracture risk may have been underestimated. The NOF guidelines were developed and validated in postmenopausal women and men aged at least 50 years, so the NOF estimates derived in this study should be viewed more in terms of the difference between groups rather than the absolute risk in each group. Lastly, FRAX and the NOF guidelines have not been validated in HIV-infected populations.
Our study has limitations. Our cohort was at low overall risk (average age 45 years, predominantly male) for bone-related harm as demonstrated by small BMD changes, with limited statistical power to determine predictors of change. In addition, as participants were on different regimens when entering the study, the sizes of the different sub-populations according to their baseline NRTI and PI agents were small, with attenuated statistical power for secondary analyses. The relatively short duration of the study and the small sample size did not allow for investigation of fractures and a possible association with the risk factors found. DXA scans were not centrally read to minimise measurement variability. An earlier time-point (e.g. 4 weeks) for BTM measurement may have provided more insight into the early pathophysiological effect of ART on bone metabolism.
Our study suggests that HIV-infected adults may benefit from assessment of risk factors associated with fractures prior to switching to TDF-FTC because of the associated higher bone turnover, and adults with a low fat mass are at higher risk for bone loss. In addition, measurement of P1NP might be useful in predicting greater hip bone loss with TDF-FTC, but this requires confirmation in larger studies.
A randomised, open-label trial to assess the safety and efficacy of switching to fixed-dose tenofovir-emtricitabine or abacavir-lamivudine: the STEAL study.
STEAL BMD Sub-Study - Concept Sheet.
The content is solely the responsibility of the authors and the views expressed in this publication do not necessarily represent the position of the Australian Government.
Clinicaltrials.gov Registration Number: NCT00192634
These results were presented at the 6th IAS Conference on HIV Pathogenesis, Treatment and Prevention (IAS 2011) 17–20 July 2011, Rome, Italy and at the 13th International Workshop on Adverse Drug Reactions and Co-morbidities in HIV 14–16 July 2011, Rome, Italy.
STEAL Study Group (as listed in )
STEAL study investigators – Anthony Allworth, Jonathan Anderson, David Baker, Mark Bloch, Mark Boyd, John Chuah, David Cooper, Stephen Davies, Linda Dayan, William Donohue, Nicholas Doong, Dominic Dwyer, John Dyer, Robert Finlayson, Michelle Giles, David Gordon, Mark Kelly, Nicholas Medland, Richard Moore, David Nolan, David Orth, Jeffrey Post, John Quin, Tim Read, Norman Roth, Darren Russell, David Shaw, David Smith, Don Smith, Alan Street, Ban Kiem Tee, Ian Woolley.
We extend our grateful thanks to all the participants, study co-ordinators and to Greg Ward for assistance with BTM assays.Samples for this project were provided by the Immunovirology Research Network of the Australian Centre for Hepatitis and HIV Virology Research. Fracture risk assessment was performed using FRAX - WHO Fracture Risk Assessment Tool, http://www.shef.ac.uk/FRAX/.
Conceived and designed the experiments: HH JH PE SE AC. Performed the experiments: SE PE. Analyzed the data: HH JA. Contributed reagents/materials/analysis tools: PE. Wrote the paper: HH JH.
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