Associations between vitamin D metabolites, antiretroviral therapy and bone mineral density in people with HIV

Osteoporos Int. 2016 May;27(5):1737-45. doi: 10.1007/s00198-015-3432-3. Epub 2015 Dec 11.

Abstract

Rationale: To see if vitamin D and antiretroviral therapy are associated with bone mineral density (BMD) in people with HIV.

Result: Lower hip BMD was associated with tenofovir (an antiretroviral medicine) in those with 25(OH)D ≥50 nmol/L.

Significance: The relationship between antiretroviral therapy and hip BMD differs depending on vitamin D status.

Introduction: People with HIV have an increased risk of low BMD and fractures. Antiretroviral therapy contributes to this increased risk. The aim of this study was to evaluate associations between vitamin D metabolites and antiretroviral therapy on BMD.

Methods: The simplification of antiretroviral therapy with tenofovir-emtricitabine or abacavir-lamivudine trial (STEAL) was an open-label, prospective randomised non-inferiority study that compared simplification of current nucleoside reverse transcriptase inhibitors (NRTIs) to fixed-dose combination tenofovir-emtricitabine (TDF-FTC) or abacavir-lamivudine. Serum 25(OH)D and 1,25(OH)2D were measured in 160 individuals (90 receiving TDF-FTC, 70 receiving other NRTIs) at baseline from this study. Multivariable linear regression models were constructed to evaluate the covariates of 1,25(OH)2D and BMD.

Results: Protease inhibitor use (p = 0.02) and higher body mass index (BMI) (p = 0.002) were associated with lower 1,25(OH)2D levels in those with 25(OH)D <50 nmol/L. However, TDF-FTC use (p = 0.01) was associated with higher 1,25(OH)2D levels, but only in those with 25(OH)D ≥50 nmol/L. White ethnicity (p = 0.02) and lower BMI (p < 0.001) in those with 25(OH)D <50 nmol/L and with TDF-FTC use (p = 0.008) in those with 25(OH)D ≥50 nmol/L were associated with lower hip BMD. TDF-FTC use, higher serum calcium and serum βCTX, winter, and lower bone-specific alkaline phosphatase (BALP) and BMI were associated with lower lumbar spine BMD.

Conclusion: TDF-FTC use (versus non-TDF-FTC use) was associated with lower hip BMD, and this difference was more pronounced in those with 25(OH)D ≥50 nmol/L. Serum 25(OH)D <50 nmol/L was associated with lower hip BMD in all participants. Therefore, the associations between antiretroviral therapy and hip BMD differ depending on vitamin D status.

Keywords: Antiretroviral therapy; Bone; HIV; Vitamin D.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anti-HIV Agents / adverse effects*
  • Anti-HIV Agents / therapeutic use
  • Body Mass Index
  • Bone Density / drug effects
  • Bone Density / physiology
  • Calcitriol / blood*
  • Dideoxynucleosides / adverse effects
  • Dideoxynucleosides / therapeutic use
  • Drug Combinations
  • Emtricitabine / adverse effects
  • Emtricitabine / therapeutic use
  • Female
  • HIV Infections / blood
  • HIV Infections / drug therapy*
  • HIV Infections / physiopathology
  • Hip Joint / physiopathology
  • Humans
  • Lamivudine / adverse effects
  • Lamivudine / therapeutic use
  • Male
  • Middle Aged
  • Osteoporosis / blood
  • Osteoporosis / chemically induced*
  • Osteoporosis / physiopathology
  • Prospective Studies
  • Tenofovir / adverse effects
  • Tenofovir / therapeutic use
  • Vitamin D / analogs & derivatives*
  • Vitamin D / blood

Substances

  • Anti-HIV Agents
  • Dideoxynucleosides
  • Drug Combinations
  • abacavir, lamivudine drug combination
  • Vitamin D
  • Lamivudine
  • Tenofovir
  • 25-hydroxyvitamin D
  • Calcitriol
  • Emtricitabine