HIV Clinical Trial
Official title:
MULTICENTRE STUDY TO ASSESS CHANGES IN BONE MINERAL DENSITY OF THE SWITCH FROM TENOFOVIR TO ABACAVIR IN HIV-1-INFECTED SUBJECTS WITH LOSS OF BONE MINERAL DENSITY
Most of studies have not found any consistent drug-specific association with bone loss and controversial data with respect the effect of protease inhibitors (PIs) have been published. The more evident finding with respect to this issue is the more pronounced decrease of bone mineral density (BMD) in patients during the first weeks of receiving a tenofovir (TDF)-containing regimen, probably by the effect of TDF on phosphorus balance and vitamin D metabolism.
The prevalence of osteoporosis in HIV-infected patients could be more than three times
greater compared with HIV-uninfected subjects, according to the results of a meta-analytical
review of cross-sectional published studies. The analysis includes data from 884
HIV-infected patients and 654 HIV-uninfected controls. Sixty-seven percent of HIV population
had reduced bone mineral density (BMD), of whom 15% had osteoporosis (OR of 6.4 and 3.7,
respectively, compared with HIV-uninfected controls).
In the same meta-analysis, when authors evaluated the role of antiretroviral therapy (ART)
on BMD, comparing 202 antiretroviral-naive with 824 ART-treated patients, patients on
treatment had a 2.5-fold increased odds of prevalent reduced BMD and osteoporosis. And
finally, when 410 non-protease inhibitor (PI)-treated HIV patients were compared with 791
patients receiving a PI-containing regimen, those on PIs had increased odds of reduced BMD
and osteoporosis.
As well, other studies support data of an impaired BMD in HIV-infected patients after
starting antiretroviral therapy. These results let us confirm that HIV itself and
antiretroviral therapy contribute to decrease the BMD.
However, most of studies have not found any consistent drug-specific association with bone
loss and controversial data with respect the effect of PIs have been published. The more
evident finding with respect to this issue is the more pronounced decrease of BMD in
patients during the first weeks of receiving a tenofovir (TDF)-containing regimen, probably
by the effect of TDF on phosphorus balance and vitamin D metabolism.
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