Vitamin D and bone loss in HIV

Corrilynn O Hileman, Edgar T Overton, Grace A McComsey, Corrilynn O Hileman, Edgar T Overton, Grace A McComsey

Abstract

Purpose of review: Bone health has become an increasingly important aspect of the care of HIV-infected patients as bone loss with antiretroviral therapy (ART) initiation is significant and osteopenia and osteoporosis are highly prevalent. Vitamin D is tightly linked to calcium balance and bone health, and vitamin D deficiency is common in HIV. This review outlines the epidemiology of vitamin D deficiency in HIV, summarizes our current understanding of the relationship between vitamin D and bone loss in HIV and the impact of vitamin D supplementation in this patient group.

Recent findings: Although data are conflicting as to whether vitamin D deficiency is more prevalent among HIV-infected individuals than in the general population, there are several reasons for why this patient group may be at heightened risk. Studies linking vitamin D deficiency to bone loss in HIV are limited; however, data from randomized clinical trials suggest a benefit of vitamin D supplementation for the prevention of bone loss with ART initiation and for the treatment of bone loss with bisphosphonate therapy.

Summary: There are too limited data to recommend universal screening of vitamin D status or supplementation to all HIV-infected individuals. However, testing 25-hydroxyvitamin D levels in those at risk for deficiency and treating patients found to be deficient or initiating ART or bisphosphonate therapy should be considered. Further study on vitamin D supplementation is needed regarding the potential benefit on immune activation and restoration in this patient group.

Trial registration: ClinicalTrials.gov NCT01523496.

Conflict of interest statement

Conflicts of interest

COH has served on a medical advisory board for Gilead Sciences. GAM has received research grants from BMS, Gilead Sciences and GSK, has served as a consultant to BMS, GSK, Janssen, Merck and Gilead, as a speaker for BMS, GSK and Tibotec and on the DSMB for a Pfizer-sponsored trial. ETO has no conflicts of interest.

Source: PubMed

3
S'abonner