Vitamin D and Calcium Supplementation Reverses Tenofovir-Caused Bone Mineral Density Loss in People Taking ART or PrEP: A Systematic Review and Meta-Analysis

Introduction

Oral antiretroviral (ART) medications have been widely applied in clinical practices to treat HIV and AIDS and to prevent HIV transmission among high-risk groups who were taking pre-exposure prophylaxis (PrEP). Medications that contain TDF (tenofovir disoproxil fumarate) were the most commonly used ART medications for people living with HIV/AIDS (PLWHA) and accounted for ~63.1% of ART medication use (1, 2). Moreover, TDF-based drugs could be used as a single-medication regimen for PrEP prevention, and it was recommended by US Centers for Disease Control and Prevention (CDC) and the WHO (3–5). However, studies reported that people who took TDF drugs have had the side effect of bone density decrease (6). The bone loss fluctuated between 2 and 6% yearly during the first year of ART initiation (7–9), and more severe outcomes included osteoporosis and fragility fractures (10, 11). Studies found that bone mineral density (BMD) loss was associated with PrEP compliance (12–14); therefore, this side effect became a barrier for PrEP receipt. One study reported that 42.9% of men who have sex with men were not willing to use PrEP because of the fear of reduced BMD (15).

Although the mechanisms of how TDF could have caused BMD loss have not been fully explained in the literature, we underlined some possible pathways to indicate this process based on current evidence. TDF could increase the level of parathyroid hormone (PTH), decrease the level of fibroblast growth factor 23 (FGF23), and affect the levels of some serum bone turnover markers [such as, C-terminal telopeptides (CTX), bone alkaline phosphatase (BAP), osteocalcin (OC), and 25-hydroxy vitamin D (25-OHD)](16, 17), which in turn caused BMD loss. Oral vitamin D (VD) and calcium supplementation could alleviate this effect on BMD through changing the levels of endocrine and bone turnover markers (12, 18) (Figure 1).

FIGURE 1

Figure 1. Possible mechanisms of how TDF caused BMD reduction and how oral vitamin D and calcium supplementation alleviated BMD reduction. TDF, Tenofovir disoproxil fumarate; PTH, parathyroid hormone; FGF23, fibroblast growth factor 23; CTX, C-terminal telopeptides; BAP, bone alkaline phosphatase; OC, osteocalcin; 25-(OH)D, 25-hydroxy vitamin D; BMD, bone mineral density.

Some placebo-controlled, randomized controlled trials (RCTs) and observational studies have investigated the effects of VD and calcium supplementation on the recovery of bone loss (19–25). However, literature did not have conclusive results without meta-analysis and systematic review studies' support. Also, no dose-response relationship has been reported. One study found that VD3 plus calcium supplements mitigates the BMD loss in HIV-positive populations who initiated TDF (25). Another study found similar results in HIV-negative populations taking PrEP (21). However, other studies did not find significant differences in changes of the hip and lumbar bone density among people living with HIV/AIDS (PLWHA) in both the VD and calcium supplementation group and the placebo group (26). Another study reported that there was no difference in the lumbar spine BMD in HIV-negative participants who participated in PrEP studies (−2.11 vs. −2.14%, p = 0.40) (27). The sample sizes were small and these studies were conducted in small regions, so that the generalizability of these findings was limited. Furthermore, the optimal amount of VD and calcium and the duration of supplementation remained unknown.

Therefore, to fill in the knowledge gaps, a systematic review and meta-analysis were performed to evaluate the effects of VD and calcium supplementation and factors associated with BMD recovery among people who were taking TDF-based drug. In addition, we investigated the dose-response relationships among the dose of VD and calcium supplements, length of supplementation, and BMD changes. The findings could be used to guide clinical practices for TDF-drug prescription and management of the TDF-drug-related BMD loss in both PLWHA and HIV-negative people who take PrEP.

Methods

Search Strategies and Selection Criteria

This systematic review was registered at the PROSPERO (International Prospective Register of Systematic Reviews) (No. 42021231000) (28).

We searched PubMed, Web of Science, Cochrane library, and EMBASE databases from the inception date to March 5, 2021, using the keywords calcium, vitamin D, Tenofovir, and bone mineral density (BMD), without language restrictions. We searched studies that investigated VD and calcium supplements and BMD in PLWHA who took TDF or HIV-negative population who took Tenofovir/Emtricitabine for PrEP. We used the index term (((‘Vitamin D') OR (‘vitamin-D') OR (VitD) OR (‘Vit-D') OR (VD)) OR ((Calcium) OR (Ca))) AND (((Tenofovir) OR (‘Tenofovir disoproxil fumarate') OR (‘tenofovir disoproxil') OR (TDF)) OR ((‘Antiretroviral Therapy') OR (‘antiretroviral therapy') OR (ART) OR (HAART) OR (‘antiretroviral treatment') OR (‘Antiretroviral-Treated'))) AND (((‘Bone Density') OR (‘bone mineral density') OR (BMD) OR (‘bone density') OR (Osteoporosis) OR (‘bone loss') OR (‘bone rarefaction') OR (‘skeletal rarefaction') OR (OP) OR (‘rarefaction of bone') OR (‘Bone fractures') OR (fracture))) for the search. We also included eligible studies through screening of the references of relevant studies and reviews. Moreover, we contacted authors to obtain articles that were not available online.

Studies were selected based on the following inclusion criteria: (1) participants were patients who are HIV-1 positive or key populations who took PrEP drugs; (2)participants used TDF-based drugs; (3) studies investigated VD or calcium supplements; (3) studies reported the outcomes of BMD for a z-score or a t-score; (4) studies had a control group. Exclusion criteria were (1) studies used indirect measures [e.g., 25 (OH) D)]; (2) studies reported the outcomes by absolute values instead of changes of BMD; (3) the detection site was neither spine nor hip. All study titles and abstracts were screened by two reviewers (XYB and FL) independently. Disagreements were resolved through consensus.

Commonly, VD and calcium were given orally and BMD was measured by a dual-energy X-ray absorptiometry (DXA General Electric Healthcare, Madison, WI, USA) scan. A DXA scan was generally read in a blinded fashion using a standardized protocol (29). A clinically significant change was defined as a decline of ≥3.0% for the lumbar spine and ≥4% for the femoral neck and total hip (27). Adverse effects associated with VD supplementation were also collected for the selected studies.

Data Analysis

Two reviewers extracted the following data independently from the 9 eligible studies: lead author, year of publication, intervention and control regimens, VD dosing, changes of BMD, and study duration. The participants' baseline characteristics were also collected including age, sex, continent of origin, and ART drugs. Disagreements were resolved by consensus.

The 9 studies were assessed using measures and criteria at the Cochrane Handbook for Interventions for quality control (18). Measures that were used to evaluate the study quality included randomization sequence generation, allocation concealment, blinding of participants and research personnel, blinding of outcome assessment, outcome data completion, selectivity of reporting, and other measures that could possibly lead to biases. All eligible studies were rated as high quality (A), moderate quality (B), or low quality (C). In addition, the Newcastle-Ottawa Scale (NOS) was used to evaluate all non-RCT studies (30). Measures that were used to evaluate biases in each study included selection, comparability, and exposure using a score ranging from 0 to 10. Discrepancies were resolved by consensus of two reviewers.

The changes of spine and hip BMD were the primary outcome. Previous studies concluded that there was a 2 to 6% hip and spine BMD loss at the first 24 to 48 weeks of ART initiation (7, 31, 32), which potentially was caused by TDF-based drugs (33).

Statistical heterogeneity between studies was assessed using an I2 scoring system. An I2 score of >50% was considered significant heterogeneity. The units we included were different, so we calculated the absolute risks by multiplying SMD and its 95% CI with the baseline risk. To assess the possible modification effect of clinical characteristics on the relationship of VD supplements and BMD, subgroup analyses were performed, including levels of detection site, HIV infection status, continent of origin, doses of VD and calcium, study duration, age, and gender by random effects. A sensitivity analysis was performed for studies with high- and moderate- quality. In addition, studies that recruited participants under specific conditions or tasks were excluded from the sensitivity analysis. The Egger's test was used to assess possible publication bias.

All meta-analyses were performed using the Stata 16 and Review Manager (5.3) for forest map and sub-group analysis. Additionally, we used the SAS (9.4) for the locally weighted regression (loess) method to assess the dose-response relationships between VD and calcium supplementation, study duration, and changes of BMD. All tests were 2-tailed with a statistical significance level of p < 0.05.

Results

Study Retrieval and Selection

Using the search strategies, we identified 3,179 studies. After the removal of duplicates, 2,554 unique records were screened, and 16 full-text were assessed for eligibility. We excluded 9 studies for the following reasons: duplicate publications (2), no available BMD data (1), different unit was used (1), self-controlled studies (2), full text unavailability (3). Seven studies were identified. The full texts of the seven articles were carefully reviewed, and all of them met the inclusion criteria. Finally, we included seven studies in the analyses (Figure 2). A summary of the seven studies was included in Table 1.

FIGURE 2

Figure 2. Literature search and study selection process. ** means the records irrelevant to the subject (n = 2538).

TABLE 1

Table 1. Characteristics of the included trials and participants.

The seven studies (13–15, 17–20) were conducted in three countries and enrolled 703 participants (median 118, range 18–188, IQR 39–165). Studies included men (86.9%) and women participants who aged from 13 to 65 years old. Five studies (13–15, 17–19) were intervention trials, and one (20) was prospective cohort study. We included participants who were HIV positive and treated using TDF (California, USA) (N = 5 36) and HIV-negative participants who were under Tenofovir/Emtricitabine PrEP (N = 167), and all of them were supplemented with VD (Tishcon, Westbury, New York or Charoon Bhesaj, Thailand; ranging from 400 to 4,000 IU/D) and calcium (ranging from 0 to 1,500 mg/D). The median follow-up duration across studies was 48 weeks (ranging from 24 to 48 weeks). All studies detected changes of spine BMD, and five of them (15, 17–20) reported changes in hip BMD. All studies were determined as a low-risk level of biases (Supplementary Table 1).

Meta-Analysis

Each of the seven studies had a VD and calcium supplementation group and a placebo or non-treatment group. There was a significant positive correlation between VD supplementation and BMD increase, as shown in Figure 3 (SMD 0.43, 95% CI 0.25 to 0.61, p = 0.009).

FIGURE 3

Figure 3. Meta-analysis results of vitamin D supplementation on BMD changes.

Subgroup Analysis

Substantial heterogeneity (I² = 55%) was used as a functional outcome. We conducted multiple subgroups and sensitivity analyses to examine the effects of oral VD and calcium supplementation on BMD changes by participants' continent, age, sex, site of detection, and study-related factors. Functional outcomes were significantly better among people whose VD supplement was 4,000 IU/D (SMD, 0.30; 95% CI, 0.02–0.58, p = 0.006). In subgroup analyses, there were no differences in treatment outcomes regarding age (p = 0.42), sex (p = 0.48), HIV infection status (p = 0.89), continent (p = 0.1), and site of detection (p = 0.45, Table 2 and Figure 4).

TABLE 2

Table 2. Subgroup analysis of association between vitamin D supplementation and BMD changes.

FIGURE 4

Figure 4. Subgroup analysis of the association between vitamin D supplementation dosing and BMD increase.

Dose-Response Relationship

This study found positive correlations between VD and calcium supplementation, study duration, and BMD increases (Figure 5). Participants' BMD showed a gradual increase with the increase of VD supplementation at the range of 50,000 IU/4 W to 4,000 IU. A VD3 daily dosing of 4,000 IU was identified as the optimal dose. There was a positive correlation between supplementary the time and the increase of BMD within 48 weeks.

FIGURE 5

Figure 5. Correlations among vitamin D supplement, treatment duration, and the changes of BMD (The corresponding articles were included in Supplementary Table 2). (A) Dose-response relationship between vitamin D and calcium supplementation and BMD changes. (B) Dose-response relationship between treatment duration and BMD changes.

Sensitivity Analysis and Publication Bias

Sensitivity analyses suggested that the effect size of the studies was within the 95% confidence interval (Supplementary Figure 1), which indicated that the study results were stable. The heterogeneity score for this meta-analysis was 55%, which implied a moderate heterogeneity. The funnel plot and the Egger's asymmetry test were used to evaluate the publication bias. The Egger's asymmetry test results showed no evidence of publication bias (p = 0.700, Supplementary Figure 2).

Discussion

This study concluded that VD supplement was significantly associated with the recovery of BMD in people who took TDF-based drugs through meta-analysis. We also found a dose-response relationship between VD supplement dosage, supplementary length, and the recovery of BMD, and the optimal dosage of VD supplement was 4 000 IU cholecalciferol (VD3) per day. BMD continuously increased up to 48 weeks of VD supplement. These findings filled in the knowledge gaps and provided useful guidance for HIV clinical doctors to treat BMD loss in participants who use TDF-based regimens. The findings in this study may help to remove concerns about potential PrEP side effects on BMD, therefore improving the receipt of PrEP.

This study indicated that compared with non-supplementation group, the BMD in people who used VD could be improved to a normal level, which was a pooled SMD of 0.43. Some clinicians recommended to prescribe upgraded ART drugs to eliminate the potential risks (34–36). Also the updated guidelines for PrEP in the United States recommended the use of updated PrEP drugs (emtricitabine/tenofovir alafenamide [Descovy^® F/TAF]) (37) because of its less side effect on bone and good efficacy (38). However, these updated drugs were more expensive. The price of TDF in China was ¥1,980 RMB/bottle (30 tablets), while that of TAF was ¥2,280 RMB (30 tablets). People must spend ¥3,600 RMB more for one-year intake of TAF. Moreover, the price of VD was ¥44.7 RMB/bottle (30 tablets) and ¥536.4 for one-year intake. The TAF regimen was 6.7 times of TDF plus VD solution. Therefore, our study indicated that VD supplementation could provide a cost-saving solution for people who had a long-term use of TDF drugs, especially for people in developing countries and regions with limited resources. Also, it was suggested to add the supplementation of VD and calcium into clinical guidelines to improve treatment outcomes.

The subgroup analysis and dose-response relationship analysis demonstrated that some factors were associated with VD supplement and BMD recovery in people who took TDF drugs. First, we found that people who used high-dose and long-time VD had better BMD recovery. Additionally, we found that there was a dose-response relationship between dose, supplement duration, and BMD changes for the range of 0–4,000 IU VD supplement per day within 48 weeks. It meant that taking 4,000 IU per day for 48 weeks could help increase the BMD continuously. Moreover, this study did not find drug toxicity and side effects in people who took high VD doses and used VD for longer time. In addition, we found that the results did not differ in terms of age, gender, country, HIV infection status, and site of detection. There were two possible reasons. First, these factors were not associated with BMD. Second, possible relationships were not detected due to the small sample size and short study duration of these studies. Therefore, future meta-analysis studies could re-evaluate the relationships by including more participants and long-duration studies.

The study had strengths. This systematic review was conducted following a prespecified and registered protocol using Cochrane methodology, which ensured a good validity. Also, we performed a comprehensive search with including multiple databases and clinical trial registries. The search did not restrict on languages and publication status of the trials. Likely, we included all available literature on this topic. In addition, to our knowledge, this was the first study that concluded on relationships among BMD changes over time, VD dosing, and the optimal VD dose and prescription time.

The study had limitations. First, a few studies that used intermediate indicators such as parathyroid hormone (PTH) and procollagen I N-terminal peptide (PINP) as measures of BMD were excluded. Bias could possibly occur due to the exclusion of these studies. Second, the studies that were included in the current meta-analysis had small sample sizes. Each study included <250 participants with a total of 703 participants for this meta-analysis. However, this study was able to detect significant relationships among variables although the sample size was small.

In conclusion, our meta-analysis synthesized findings of current studies about the effects of VD and calcium supplementation on the recovery of BMD and indicated that VD supplementation improved BMD. The study provided valuable implications for clinical doctors to prescribe VD for people who took TDF-based drugs to reverse its effect of BMD loss. A daily supplement dosing of 4,000 IU of VD that could achieve the optimal outcome was recommended. Moreover, it was a cost-saving method and could be applied in HIV treatment facilities and PrEP prevention programs especially in resource-limited settings.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.

Author Contributions

XB and JX conceived and designed the study, analyzed the data, and interpreted results. XB and FL acquired the data, screened records, extracted data, and assessed risks of biases. XB designed the literature search and conducted the statistical analyses. XB, FL, JX, XZ, HW, XH, KY, ZY, WG, and HD wrote, revised, and interpreted the study results of the manuscript. All authors have read and approved the final manuscript before the submission.

Funding

This work was supported by the National Natural Science Foundation of China (81872674), the Mega-Projects of National Science Research [13th Five-Year Plan (2017ZX10201101-002-007)], the Beijing Excellent Talent Plan (2018000021223ZK04), and National Science and Technology Major Project (2018ZX10101).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Acknowledgments

The authors would like to thank all clinicians and research staff who have contributed to this study for their efforts.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnut.2022.749948/full#supplementary-material

References

1. Manosuthi W, Ongwandee S, Bhakeecheep S, Leechawengwongs M, Ruxrungtham K, Phanuphak P, et al. Guidelines for antiretroviral therapy in HIV-1 infected adults and adolescents 2014, Thailand. AIDS Res Ther. (2015) 12:12. doi: 10.1186/s12981-015-0053-z

PubMed Abstract | CrossRef Full Text

2. Biver E, Calmy A, Aubry-Rozier B, Birkhauser M, Bischoff-Ferrari HA, Ferrari S, et al. Diagnosis, prevention, and treatment of bone fragility in people living with HIV: a position statement from the Swiss Association against Osteoporosis. Osteoporosis Int. (2019) 30:1125–35. doi: 10.1007/s00198-018-4794-0

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Centers for Disease Control and Prevention (CDC). Interim guidance for clinicians considering the use of preexposure prophylaxis for the prevention of HIV infection in heterosexually active adults. MMWR Morbidity Mortality Wkly Rep. (2012) 61:586–9.

Google Scholar

4. Eriksen J, Albert J, Blaxhult A, Carlander C, Flamholc L, Gisslén M, et al. Antiretroviral treatment for HIV infection: swedish recommendations 2016. Infect Dis. (2017) 49:1–34. doi: 10.1080/23744235.2016.1247495

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Wattanachanya L, Jantrapakde J, Avihingsanon A, Ramautarsing R, Kerr S, Trachunthong D, et al. Antiretroviral-naïve HIV-infected patients had lower bone formation markers than HIV-uninfected adults. AIDS Care. (2020) 32:984–93. doi: 10.1080/09540121.2019.1622631

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Zhang Q, Liu X, Hu P. Suboptimal response, elder and comorbidity are decisive elements for choosing tenofovir alafenamide (TAF): a real-world study in southwest of China. Hepatol Int. (2020) 14:S60. doi: 10.1007/s12072-020-10030-4

CrossRef Full Text | Google Scholar

7. Stellbrink H, Orkin C, Arribas J, Compston J, Gerstoft J, Van Wijngaerden E, et al. Comparison of changes in bone density and turnover with abacavir-lamivudine versus tenofovir-emtricitabine in HIV-infected adults: 48-week results from the ASSERT study. Clin infect Dis. (2010) 51:963–72. doi: 10.1086/656417

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Duvivier C, Kolta S, Assoumou L, Ghosn J, Rozenberg S, Murphy R, et al. Greater decrease in bone mineral density with protease inhibitor regimens compared with nonnucleoside reverse transcriptase inhibitor regimens in HIV-1 infected naive patients. AIDS. (2009) 23:817–24. doi: 10.1097/QAD.0b013e328328f789

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Guo F, Song X, Li Y, Guan W, Pan W, Yu W, et al. Longitudinal change in bone mineral density among Chinese individuals with HIV after initiation of antiretroviral therapy. Osteoporosis Int. (2021) 32:321–32. doi: 10.1007/s00198-020-05584-w

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Zeng Y, Xiao J, Li C, Wang Y, Zhang L, Pang X, et al. Prevalence and risk factors for bone mineral density changes in antiretroviral therapy-naive human immunodeficiency virus-infected adults: a Chinese cohort study. Chin Med J. (2020) 133:2940–6. doi: 10.1097/CM9.0000000000001317

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Havens PL, Perumean-Chaney SE, Patki A, Cofield SS, Wilson CM, Liu N, et al. Changes in bone mass after discontinuation of preexposure prophylaxis with tenofovir disoproxil fumarate/emtricitabine in young men who have sex with men: extension phase results of adolescent trials network protocols 110 and 113. Clin Infect Dis. (2020) 70:687–91. doi: 10.1093/cid/ciz486

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Han W, Wattanachanya L, Apornpong T, Jantrapakde J, Avihingsanon A, Kerr S, et al. Bone mineral density changes among people living with HIV who have started with TDF-containing regimen: a five-year prospective study. PLoS ONE. (2020) 15:e0230368. doi: 10.1371/journal.pone.0230368

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Xu Z, He P, Xian J, Lu W, Shu J, Luo W, et al. Association between nonalcoholic fatty liver disease and bone mineral density in HIV-infected patients receiving long-term TDF-based antiretroviral therapy. Curr HIV Res. (2021) 19:40–6. doi: 10.2174/1570162X18999200917120449

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Xu J, Tang W, Zhang F, Shang H. PrEP in China: choices are ahead. Lancet HIV. (2020) 7:e155–7. doi: 10.1016/S2352-3018(19)30293-0

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Cressey T, Siriprakaisil O, Kubiak R, Klinbuayaem V, Sukrakanchana P, Quame-Amaglo J, et al. Plasma pharmacokinetics and urinary excretion of tenofovir following cessation in adults with controlled levels of adherence to tenofovir disoproxil fumarate. Int J Infect Dis. (2020) 97:365–70. doi: 10.1016/j.ijid.2020.06.037

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Matuszewska A, Nowak B, Nikodem A, Jedrzejuk D, Szkudlarek D, Zduniak K, et al. Effects of efavirenz and tenofovir on bone tissue in Wistar rats. Adv Clin Exp Med. (2020) 29:1265–75. doi: 10.17219/acem/127684

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Nickolas TL, Yin MT, Hong T, Mugwanya KK, Branch AD, Heffron R, et al. Impact of tenofovir-based pre-exposure prophylaxis on biomarkers of bone formation, bone resorption, and bone mineral metabolism in HIV-negative adults. Open Forum Infect. Dis. (2019) 6:ofz338. doi: 10.1093/ofid/ofz338

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Jo S, Yoon S, Nam SW, Yang JH, Sung IH, Kim TH. 1,25D3 promotes mineralization of osteoblasts by activating C/EBPβ-DKK1 axis. Arthritis Rheumatol. (2019) 71:3905–6. doi: 10.1002/art.41108

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Mela Q, Ruggiero V, Montaldo L, Pisano U, Matta L, Maria Pasetto C, et al. Bone mass preservation with high-dose cholecalciferol and dietary calcium in HIV patients following antiretroviral therapy. Is it possible? HIV Clin Trials. (2018) 19:188–96. doi: 10.1080/15284336.2018.1525841

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Puthanakit T, Wittawatmongkol O, Poomlek V, Sudjaritruk T, Brukesawan C, Bunupuradah T, et al. Effect of calcium and vitamin D supplementation on bone mineral accrual among HIV-infected Thai adolescents with low bone mineral density. J Virus Eradic. (2018) 4:6–11. doi: 10.1016/S2055-6640(20)30234-X

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Pornpaisalsakul K, Songtaweesin WN, Tepmongkol S, Wongharn P, Kawichai S, Suponsilchai V, et al. Effects of vitamin D and calcium supplementation on bone mineral density among Thai youth using daily HIV pre-exposure prophylaxis. J Int AIDS Soc. (2020) 23:e25624. doi: 10.1002/jia2.25624

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Nct high dose vitamin D Calcium for Bone Health in Individuals Initiating HAART. (2011). Available online at: https://clinicaltrials.gov/show/NCT01403051 (accessed October 23, 2020).

Google Scholar

23. Bech A, Van Bentum P, Telting D, Gisolf J, Richter C, De Boer H. Treatment of calcium and vitamin D deficiency in HIV-positive men on tenofovir-containing antiretrovial therapy. HIV Clin Trials. (2012) 13:350–6. doi: 10.1310/hct1306-350

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Havens PL, Stephensen CB, Van Loan MD, Schuster GU, Woodhouse LR, Flynn PM, et al. Vitamin D3 supplementation increases spine bone mineral density in adolescents and young adults with human immunodeficiency virus infection being treated with tenofovir disoproxil fumarate: a randomized, placebo-controlled trial. Clin Infect Dis. (2018) 66:220–8. doi: 10.1093/cid/cix753

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Overton ET, Chan ES, Brown TT, Tebas P, McComsey GA, Melbourne KM, et al. Vitamin D and calcium attenuate bone loss with antiretroviral therapy initiation: a randomized trial. Ann Intern Med. (2015) 162:815–24. doi: 10.7326/M14-1409

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Boontanondha P, Nimitphong H, Musikarat S, Ragkho A, Kiertiburanakul S. Vitamin D and calcium supplement attenuate bone loss among HIV infected patients receiving tenofovir disoproxil fumarate/emtricitabine/ efavirenz: an open-label, randomized controlled trial. Curr HIV Res. (2020) 18:52–62. doi: 10.2174/1570162X18666200106150806

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Kortenaar JL, Cheung A, Mewa S, Waugh E, Rubin L, Tan D. Exploring strategies for attenuating changes in bone mineral density in MSM on TDF/FTC HIV pre-exposure prophylaxis. Open Forum Infect Dis. (2017) 4:S220. doi: 10.1093/ofid/ofx163.452

CrossRef Full Text | Google Scholar

28. PROSPERO (2021). Available online at: https://www.crd.york.ac.uk/PROSPERO/ (accessed November 18, 2020).

Google Scholar

29. Slater J, Kruger R, Douwes J, O'Brien W, Corbin M, Miles-Chan J, et al. Objectively measured physical activity is associated with body composition and metabolic profiles of pacific and new zealand european women with different metabolic disease risks. Front Physiol. (2021) 12:684782. doi: 10.3389/fphys.2021.684782

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Wells GA, Shea B, O'Connell D, Peterson J, Welch V, Losos M, et al. The Newcastle-Ottawa Scale (NOS) for Assessing the Quality of Non-Randomised Studies in Meta-Analyses. Available online at: http://www.ohri.ca/programs/clinical_ (accessed November 18, 2020).

PubMed Abstract | Google Scholar

31. McComsey GA, Kitch D, Daar ES, Tierney C, Jahed NC, Tebas P, et al. Bone mineral density and fractures in antiretroviral-naive persons randomized to receive abacavir-lamivudine or tenofovir disoproxil fumarate-emtricitabine along with efavirenz or atazanavir-ritonavir: AIDS Clinical Trials Group A5224s, a substudy of ACTG A5202. J Infect Dis. (2011) 203:1791–801. doi: 10.1093/infdis/jir188

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Gallant J, Staszewski S, Pozniak A, DeJesus E, Suleiman J, Miller M, et al. Efficacy and safety of tenofovir DF vs stavudine in combination therapy in antiretroviral-naive patients: a 3-year randomized trial. JAMA. (2004) 292:91–201. doi: 10.1001/jama.292.2.191

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Brown T, McComsey G. Association between initiation of antiretroviral therapy with efavirenz and decreases in 25-hydroxyvitamin D. Antiviral Ther. (2010) 15:425–9. doi: 10.3851/IMP1502

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Natukunda E, Gaur AH, Kosalaraksa P, Batra J, Rakhmanina N, Porter D, et al. Safety, efficacy, and pharmacokinetics of single-tablet elvitegravir, cobicistat, emtricitabine, and tenofovir alafenamide in virologically suppressed, HIV-infected children: a single-arm, open-label trial. Lancet Child Adolesc Health. (2017) 1:27–34. doi: 10.1016/S2352-4642(17)30009-3

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Tao X, Lu Y, Zhou Y, Zhang L, Chen Y. Efficacy and safety of the regimens containing tenofovir alafenamide versus tenofovir disoproxil fumarate in fixed-dose single-tablet regimens for initial treatment of HIV-1 infection: a meta-analysis of randomized controlled trials. Int J Infect Dis. (2020) 93:108–17. doi: 10.1016/j.ijid.2020.01.035

PubMed Abstract | CrossRef Full Text | Google Scholar

36. De Clercq E. Role of tenofovir alafenamide (TAF) in the treatment and prophylaxis of HIV and HBV infections. Biochem Pharmacol. (2018) 153:2–11. doi: 10.1016/j.bcp.2017.11.023

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Saag M, Gandhi R, Hoy J, Landovitz R, Thompson M, Sax P, et al. Antiretroviral drugs for treatment and prevention of HIV Infection in adults: 2020 recommendations of the international antiviral society-USA panel. JAMA. (2020) 324:1651–69. doi: 10.1001/jama.2020.17025

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Fields S, Tung E. Patient-focused selection of PrEP medication for individuals at risk of HIV: a narrative review. Infect Dis Ther. (2021) 10:165–86. doi: 10.1007/s40121-020-00384-5

PubMed Abstract | CrossRef Full Text | Google Scholar