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Updated: Jul 17, 2026

Expansion of Human Peripheral Blood γδ T Cells using Zoledronate
Published on: September 9, 2011
Annual zoledronate increases bone density in highly active antiretroviral therapy-treated human immunodeficiency
Mark J Bolland1, Andrew B Grey, Anne M Horne
1Department of Medicine, University of Auckland, and Department of Infectious Diseases, Auckland Hospital, New Zealand. m.bolland@auckland.ac.nz
Context:
Recent studies have reported low bone mineral density (BMD) in HIV-infected patients. Annual iv administration of 4 mg zoledronate has been shown to increase BMD and suppress bone turnover in postmenopausal women.
Objective:
The objective of the study was to determine whether annual administration of 4 mg zoledronate will increase BMD in HIV-infected men receiving highly active antiretroviral therapy.
Design And Setting:
A 2-yr randomized placebo-controlled trial was conducted in a clinical research center.
Participants:
A total of 43 HIV-infected men were treated with highly active antiretroviral therapy for at least 3 months, with BMD T score less than -0.5.
Intervention:
Participants received annual iv administration of 4 mg zoledronate or placebo. All participants took 400 mg/d calcium and 1.25 mg/month vitamin D.
Measurements:
BMD at the lumbar spine, total hip and total body, and bone turnover markers were measured.
Results:
At the lumbar spine, BMD increased by 8.9% over 2 yr in the zoledronate group compared with an increase of 2.6% in the control group (P<0.001). At the total hip, BMD increased by 3.8% over 2 yr in the zoledronate group compared with a decrease of 0.8% in the control group (P<0.001). At the total body, BMD increased by 2.3% over 2 yr compared with a decrease of 0.5% in the control group (P<0.001). Urine N-telopeptide decreased by 60% at 3 months in the zoledronate group and thereafter remained stable.
Conclusions:
Annual administration of zoledronate is a potent and effective therapy for the prevention or treatment of bone loss in HIV-infected men. The current data provide the first trial evidence of the BMD effects of annual zoledronate beyond 1 yr in any population, as well as being the first reported trial in men.
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