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Can Switching Antiretroviral Drugs Improve Vitamin D Levels?

SUMMARY: HIV positive participants in the MONET trial who switched from antiretroviral therapy (ART) regimens containing efavirenz (Sustiva) or zidovudine (AZT; Retrovir) to boosted darunavir (Prezista) experienced increases in their vitamin D levels, in some cases helping reverse deficiency, according to an analysis described in the September 21, 2010 advance online edition of AIDS Research and Human Retroviruses.

By Liz Highleyman

A number of recent studies have shown that vitamin D deficiency is common among people with HIV, even more so than the population as a whole. Low levels of vitamin D can contribute to bone loss, which in turn can lead to fractures. Among HIV negative people, low vitamin D levels have been linked to cardiovascular disease and cancer.

Julie Fox from Guys and St. Thomas NHS Trust in London and colleagues looked at vitamin D levels among participants in the European MONET trial, which compared standard ART -- consisting of a protease inhibitor or NNRTI plus a "backbone" of 2 nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) -- versus darunavir/ritonavir monotherapy.

As previously reported, MONET enrolled 256 patients who were taking a standard 3-drug ART regimen, had undetectable viral load (< 50 copies/mL), and had no history of virological treatment failure. They were randomly assigned to switch to 800/100 mg once-daily darunavir/ritonavir, either alone or in combination with 2 NRTIs. Most participants (about 80%) were men, about 90% were white, the median age was 44 years, and the median CD4 cell count of 575 cells/mm3.

At 96 weeks, more than 90% of patients who switched from a suppressive combination regimen to darunavir/ritonavir alone maintained undetectable viral load, but monotherapy was not quite as effective as 3-drug combination therapy, leading to more frequent treatment failure.

Fox and colleagues analyzed data from 221 patients who had their 25-hydroxyvitamin D levels measured before randomized treatment started and again at week 96.

Results

At the screening visit, lower vitamin D levels were significantly associated with the following factors:
 
Calendar month (P = 0.0067);
Black race/ethnicity (P = 0.013);
Use of efavirenz (P = 0.0062);
Use of zidovudine (P = 0.015).
Mean vitamin D levels were lowest from January through April (35.8 nmol/L) and highest in September (45.4 nmol/L).
Patients who discontinued efavirenz or zidovudine before starting their MONET study regimen had significantly larger increases in vitamin D between screening and week 96, compared with those who stopped other drugs.

Based on these findings, the study authors recommended, "Routine screening of HIV-positive patients for vitamin D should be considered and the optimal management further defined."

"Given the evidence for health benefits of optimal vitamin D levels, people with HIV infection should be monitored for vitamin D levels," they elaborated in their discussion. "For patients with severe vitamin D deficiency, the use of vitamin D supplements or changes in antiretroviral treatment could be considered."

"The association between use of efavirenz and vitamin D deficiency is consistent with previous cross-sectional and prospective studies," they added. "To our knowledge, this is the first report to show increases in vitamin D levels after switching from efavirenz-based antiretroviral treatment to [protease inhibitor]-based treatment."

Investigator affiliations: Guys and St Thomas NHS Trust, London, UK; Janssen-Cilag EMEA, Neuss, Germany; Hospital la Paz, Madrid, Spain; Pharmacology Research Laboratories, University of Liverpool, Liverpool, UK.

12/14/10

Reference
J Fox, B Peters, M Prakash, and others. Improvement in Vitamin D Deficiency Following Antiretroviral Regime Change: Results from the MONET Trial. AIDS Research and Human Retroviruses (Abstract). September 21, 2010 (Epub ahead of print).

 


 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


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