In patients initiating antiretroviral therapy, elevation in a bone turnover marker is linked to the magnitude of CD4 cell recovery, suggesting an immune-mediated mechanism for bone loss.
After initiation of antiretroviral therapy (ART), bone mineral density (BMD) declines abruptly for 1 to 2 years before stabilizing in most HIV-infected patients. Despite differences in the extent of the decline depending on antiretroviral regimen, some bone loss occurs regardless of regimen, suggesting a common mechanism may be at work in addition to direct drug effects. In animal studies, bone loss has been linked to T-cell reconstitution and inflammation. Now, investigators have explored whether a similar mechanism may be involved in humans.
Twenty HIV-infected patients (80% men, 90% African-American) initiated therapy with tenofovir disoproxil fumarate (TDF)/FTC and ritonavir-boosted lopinavir (the samples were collected some years ago, h…
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DisclosuresGrant/Research SupportNIH
Editorial BoardsUpToDate; ID Images (idimages.org); Infectious Diseases Society of America COVID-19 Treatment Guidelines; International Antiviral Society–USA (Guidelines Committee)
Leadership Positions in Professional SocietiesHIV Medicine Association; Infectious Diseases Society of America (Board of Directors)
DisclosuresGrant/Research SupportNIH
Editorial BoardsUpToDate; ID Images (idimages.org); Infectious Diseases Society of America COVID-19 Treatment Guidelines; International Antiviral Society–USA (Guidelines Committee)
Leadership Positions in Professional SocietiesHIV Medicine Association; Infectious Diseases Society of America (Board of Directors)