Proteoglycan Dynamics and Bone Quality: Molecular Regulation to Age-Related Fragility

Clinically, bone mineral density (BMD) accounts for only approximately 50% of the observed variance in bone fragility fractures. This review examines the dynamic and mechanistic role of the non-collagenous organic matrix, specifically proteoglycans (PGs) and glycosaminoglycans (GAGs), in maintaining bone toughness and bone quality. During aging, bulk cortical GAG levels decrease by up to ~17% and are highly associated with reduced bone tissue toughness. We analyze how this age-related loss may arise from uncoupled bone remodeling and tissue aging, including the accumulation of older, interstitial tissue and dysregulated osteocyte-mediated matrix maintenance. We then discuss the functional importance of PG/GAG composition, maturation, and catabolism and how perturbations in these processes can promote pro-inflammatory signaling that accelerates matrix degradation and contributes to systemic aging. Lastly, we discuss potential interventions to preserve or restore GAGs/PGs in bone and improve overall bone quality.

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Publication Details

Journal
Biomolecules
Published
2026-04-13
DOI
https://doi.org/10.3390/biom16040572
Primary Topic
Bone health and osteoporosis research
Type
article
Field-Weighted Citation Impact
0.00

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article

Proteoglycan Dynamics and Bone Quality: Molecular Regulation to Age-Related Fragility

X. Wang, Savannah Heath, Rui Hua, Jean X. Jiang
Biomolecules
Bone health and osteoporosis research
article

Proteoglycan Dynamics and Bone Quality: Molecular Regulation to Age-Related Fragility

X. Wang, Savannah Heath, Rui Hua, Jean X. Jiang
article en

Abstract

Clinically, bone mineral density (BMD) accounts for only approximately 50% of the observed variance in bone fragility fractures. This review examines the dynamic and mechanistic role of the non-collagenous organic matrix, specifically proteoglycans (PGs) and glycosaminoglycans (GAGs), in maintaining bone toughness and bone quality. During aging, bulk cortical GAG levels decrease by up to ~17% and are highly associated with reduced bone tissue toughness. We analyze how this age-related loss may arise from uncoupled bone remodeling and tissue aging, including the accumulation of older, interstitial tissue and dysregulated osteocyte-mediated matrix maintenance. We then discuss the functional importance of PG/GAG composition, maturation, and catabolism and how perturbations in these processes can promote pro-inflammatory signaling that accelerates matrix degradation and contributes to systemic aging. Lastly, we discuss potential interventions to preserve or restore GAGs/PGs in bone and improve overall bone quality.

BiomoleculesVol. 16(4)
The University of Texas at San Antonio Health Science Center (US), The University of Texas at San Antonio (US)
Welch Foundation
Openalex Percentile: Top 25%
Bone health and osteoporosis research
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