ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 3174

Vitamin D Binding Protein and Tenofovir-Associated Bone Loss Among Individuals with HIV

Evelyn Hsieh1,2, Liana Fraenkel1, Weibo Xia3, Yang Han2, Michael Yin4, Karl Insogna5, Ting Zhu2 and Taisheng Li2, 1Section of Rheumatology, Yale School of Medicine, New Haven, CT, 2Department of Infectious Diseases, Peking Union Medical College Hospital, Beijing, China, 3Department of Endocrinology, Peking Union Medical College Hospital, Beijing, China, 4Division of Infectious Diseases, Columbia University Medical Center, New York, NY, 5Section of Endocrinology, Yale School of Medicine, New Haven, CT

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Vitamin D and osteoporosis

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Tuesday, November 10, 2015

Title: Osteoporosis and Metabolic Bone Disease - Clinical Aspects and Pathogenesis

Session Type: ACR Concurrent Abstract Session

Session Time: 4:30PM-6:00PM

Background/Purpose:

Antiretroviral regimens containing tenofovir disoproxil fumarate (TDF) have been associated with decreases in bone mineral density, and elevations in bone turnover markers (BTM) and intact parathyroid hormone (iPTH) in patients with HIV. Prior cross-sectional studies suggested that a functional vitamin D deficiency may in part explain these changes. To explore this hypothesis further, we measured change in plasma vitamin D binding protein (DBP) levels from baseline to 48 weeks among a cohort of patients treated with TDF/lamivudine(3TC)/efavirenz(EFV) in the context of other serologic markers of vitamin D and bone metabolism.

Methods:

We performed a secondary analysis using plasma samples collected at 0, 24, and 48 weeks after initiation of TDF/3TC/EFV from 140 adult participants enrolled in a multi-center randomized trial. Women over 45 years were excluded to avoid confounding due to menopausal status. Data regarding socio-demographic characteristics, BMI, CD4+ counts, and HIV viral load were obtained as part of the parent study. Laboratory tests included plasma DBP, iPTH, total 25-hydroxyvitamin D (25OHD), the bone resorption marker collagen type 1 cross-linked C-telopeptide (CTX), and the bone formation marker total procollagen type 1 N-terminal propeptide (P1NP). Differences between time points were compared using the paired t-test and Wilcoxin signed-rank test.

Results:

Our sample included 108 men and 26 women with a mean age of 33.6±9.6 years and BMI of 22.3±2.9 kg/m2.  Mean BMI remained stable from 0 to 48 weeks (p=0.47), however median CD4+ count increased significantly from 290.5 (IQR: 201-362) to 424 (IQR: 294-555) cells/mm3 (p<0.001) and median viral load decreased from 53767 (IQR: 19802 to 136493) to 0 (IQR:0 to 10) copies/mL (p<0.001). Significant increases were observed in DBP levels from 0 to 24 weeks followed by smaller increases from 24 to 48 weeks (see Table). Similar increases were detected in iPTH levels, however 25OHD levels remained stable. BTM levels increased significantly from 0 to 24 weeks followed by a slight decline (CTX) or stabilization (P1NP), however remained significantly higher compared with baseline at 48 weeks.

Conclusion:

Plasma levels of DBP rose significantly in the first 24 weeks after initiation of TDF/3TC/EFV, followed by a more modest increase from 24 to 48 weeks. This change was observed in concert with elevations iPTH and BTMs, despite stable 25OHD levels, supporting a potential role for DBP in bone loss associated with TDF therapy.


Disclosure: E. Hsieh, None; L. Fraenkel, None; W. Xia, None; Y. Han, None; M. Yin, None; K. Insogna, None; T. Zhu, None; T. Li, None.

To cite this abstract in AMA style:

Hsieh E, Fraenkel L, Xia W, Han Y, Yin M, Insogna K, Zhu T, Li T. Vitamin D Binding Protein and Tenofovir-Associated Bone Loss Among Individuals with HIV [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/vitamin-d-binding-protein-and-tenofovir-associated-bone-loss-among-individuals-with-hiv/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2015 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/vitamin-d-binding-protein-and-tenofovir-associated-bone-loss-among-individuals-with-hiv/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology