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Osteoimmunopathology in HIV/AIDS: A Translational Evidence-Based Perspective
André Barkhordarian1, Reem Ajaj, Manisha H Ramchandani
1Section of Oral Biology, Division of Oral Biology & Medicine, UCLA School of Dentistry, Los Angeles, CA 90095, USA.
Human immunodeficiency virus-1 (HIV) infection and acquired immune deficiency syndrome (AIDS) disrupt bone metabolism, increasing osteoporosis risk. Treatments like ART, PI, and HAART may contribute to these bone density changes.
Area of Science:
- Immunology
- Endocrinology
- Bone Metabolism
Background:
- Human immunodeficiency virus-1 (HIV) infection and acquired immune deficiency syndrome (AIDS) impact cellular immunity and bone metabolism.
- The osteoimmune network highlights the connection between immune function and bone health.
- HIV/AIDS patients exhibit altered bone metabolism, contributing to increased osteoporosis prevalence.
Purpose of the Study:
- To review evidence on how HIV/AIDS affects bone metabolism.
- To discuss the role of antiretroviral therapies (ART, PI, HAART) in HIV-associated bone disease.
- To provide a translational perspective for comparative effectiveness and evidence-based interventions.
Main Methods:
- Systematic review of existing literature.
- Analysis of translational clinical evidence.
- Comparative effectiveness research framework.
Main Results:
- Evidence indicates impaired osteoblast activity and increased osteoclast activity in HIV/AIDS patients.
- Osteoporosis is significantly more prevalent in individuals with HIV/AIDS.
- Antiretroviral therapies, including protease inhibitors (PI) and highly active antiretroviral therapy (HAART), are implicated in these bone metabolic changes.
Conclusions:
- HIV/AIDS profoundly affects bone metabolism, leading to increased osteoporosis.
- Therapeutic interventions for HIV/AIDS, such as ART, PI, and HAART, warrant further investigation for their skeletal side effects.
- Global, evidence-based strategies are needed to address bone health in the context of HIV/AIDS management.
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