Bone health and chronic viral infections: A narrative literature review.

Authors

Jelena S Jadzic, Andreja B Baljozovic, Ljubica D Simic

Published in

World journal of virology. Volume 15. Issue 1. Pages 118225. Mar 25, 2026.

Abstract

Chronic viral infections, such as human immunodeficiency virus (HIV), hepatitis B (HBV), and hepatitis C (HCV), negatively impact bone health leading to osteopenia/osteoporosis and increased bone fragility. This narrative review aims to provide a comprehensive overview of the contemporary literature on bone changes in patients with chronic viral infections (HIV, HBV, HCV mono-infection, and coinfections), focusing on their clinical implications and the importance of assessing multiscale bone properties to evaluate bone strength decline in these individuals. Previous studies suggest that skeletal alterations in these subjects may arise from direct viral effects on bone cells and from indirect mechanisms involving systemic inflammation, immune dysregulation, therapy-related effects, and distant organ failure (e.g., liver disease). It has been reported that HBV/HCV co-infection in people living with HIV produces the most severe phenotype through additive inflammatory, hepatic, and metabolic insults. Further, an increased risk of developing osteonecrosis of multiple joints has also been reported among people living with HIV. Given the limited contemporary data, future studies should focus on investigating hierarchical alterations in bone structure to deepen our understanding of the complex skeletal changes in patients with chronic viral infections, thereby providing a solid foundation for advancing clinical management. As the population living with chronic viral infections ages, total joint arthroplasty will increasingly become a standard procedure, requiring a deeper understanding of how various hierarchical bone morpho-structural changes affect implant stability and longevity in these patients.

PMID:
41884453
Bibliographic data and abstract were imported from PubMed on 13 Sep 2026.

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