Ascorbic Acid Modulates Collagen Properties in Glucocorticoid‐Induced Osteoporotic Bone: Insights into Chemical, Mechanical, and Biological Regulation

Osteoporosis is a prevalent skeletal disorder characterized by decreased bone mass and structural deterioration, leading to an increased risk of fractures. This study focuses on the regulatory role of Vitamin C (ascorbic acid; AA) in the context of glucocorticoid-induced osteoporosis (GIOP), which results from long-term glucocorticoid (GC) therapy. The data showed that GCs impair AA metabolism in osteoblasts, thereby disrupting collagen synthesis and compromising extracellular matrix (ECM) integrity. Notably, AA integration in the collagen matrix improved its biochemical and mechanical properties. Additionally, it has been shown that the presence of AA restored osteoblast and endothelial function, enhanced collagen production, and improved endothelial barrier function under GC exposure. These results underscore the critical role of Vitamin C in bone matrix maintenance and homeostasis. Collectively, this work highlights the therapeutic potential of Vitamin C as a supportive treatment to counteract the deleterious skeletal effects of long-term GC therapy.

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Journal
Advanced Healthcare Materials
Published
2025-09-25
DOI
https://doi.org/10.1002/adhm.202502606
Primary Topic
Vitamin D Research Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Ascorbic Acid Modulates Collagen Properties in Glucocorticoid‐Induced Osteoporotic Bone: Insights into Chemical, Mechanical, and Biological Regulation

Joanna Kitlińska, Evagelia C. Laiakis, Peter Lialios, Meth Jayatilake et al.
Advanced Healthcare Materials
Vitamin D Research Studies
article

Ascorbic Acid Modulates Collagen Properties in Glucocorticoid‐Induced Osteoporotic Bone: Insights into Chemical, Mechanical, and Biological Regulation

Joanna Kitlińska, Evagelia C. Laiakis, Peter Lialios, Meth Jayatilake, Stella Alimperti, Y. Kim, Micaila Curtis, J. Koudy Williams, Edward Van Keuren, Mehdi syed Nouraie, Jonathan E. Seppala, Alison Grafton, Anthoula Lazaris, Rahul Patil, Xinran Zhang, Maria Bizaki, Penelope Xeron, Orelle Bulgin, Sana Surrency, Soraya Tarrah
article en

Abstract

Osteoporosis is a prevalent skeletal disorder characterized by decreased bone mass and structural deterioration, leading to an increased risk of fractures. This study focuses on the regulatory role of Vitamin C (ascorbic acid; AA) in the context of glucocorticoid-induced osteoporosis (GIOP), which results from long-term glucocorticoid (GC) therapy. The data showed that GCs impair AA metabolism in osteoblasts, thereby disrupting collagen synthesis and compromising extracellular matrix (ECM) integrity. Notably, AA integration in the collagen matrix improved its biochemical and mechanical properties. Additionally, it has been shown that the presence of AA restored osteoblast and endothelial function, enhanced collagen production, and improved endothelial barrier function under GC exposure. These results underscore the critical role of Vitamin C in bone matrix maintenance and homeostasis. Collectively, this work highlights the therapeutic potential of Vitamin C as a supportive treatment to counteract the deleterious skeletal effects of long-term GC therapy.

Advanced Healthcare MaterialsVol. 15(12)
Georgetown University (US), Georgetown University Medical Center (US), Material Measurement Laboratory (US)
George Washington University, Georgetown University, National Institutes of Health, National Institute of Standards and Technology, National Cancer Institute
Openalex Percentile: Top 63%
Vitamin D Research Studies
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