{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,2]],"date-time":"2026-06-02T05:08:19Z","timestamp":1780376899417,"version":"3.54.1"},"reference-count":300,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2026,6,2]],"date-time":"2026-06-02T00:00:00Z","timestamp":1780358400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Endocrinol."],"abstract":"<jats:p>Stress-induced upregulation of interleukin-6 (IL-6) signaling and its downstream pathophysiological consequences have garnered considerable attention in recent years. However, no comprehensive review has specifically examined the association between stress-induced IL-6 and its implications for bone health in children. During childhood, linear growth and peak bone mass acquisition are tightly regulated processes. Hence, this review aims to investigate current evidence on stress-induced IL-6 upregulation and its detrimental effects on pediatric bone health. Findings from animal models, knockout studies, pediatric inflammatory disorders, including juvenile idiopathic arthritis, pediatric systemic lupus erythematosus and inflammatory bowel disease, and models of metabolic stress collectively demonstrate that stress triggers IL-6, thereby impairing skeletal growth and increasing fragility. Data shows that persistent IL-6 upregulation not only disrupts the normal functioning of growth hormone, insulin-like growth factor-1 (GH\/IGF-1) axis, enhances receptor activator of nuclear factor kappa-B ligand (RANKL)-mediated osteoclastogenesis, and promotes bone marrow adiposity. Further, stress-induced high levels of IL-6 adversely affect the skeletal, immune, and endocrine systems, thereby compromising skeletal development and bone growth in children. Elevated systemic or local IL-6 levels may exert direct deleterious effects on bone by impairing stem cell differentiation and inhibiting the proliferation and maturation of growth plate chondrocytes, ultimately restricting longitudinal bone growth. Moreover, elevated IL-6 levels may also impair muscle health and crosstalk between muscle and bone, thereby compromising skeletal integrity. Collectively, these findings underscore the need for integrative therapeutic strategies that target inflammation and redox imbalance in bone and other tissues, particularly in children. Better understanding stress-induced IL-6 dysregulation is critical for pediatric bone development and long-term skeletal health.<\/jats:p>","DOI":"10.3389\/fendo.2026.1833900","type":"journal-article","created":{"date-parts":[[2026,6,2]],"date-time":"2026-06-02T04:28:25Z","timestamp":1780374505000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":0,"title":["Stress-induced IL-6 regulation in pediatric bone growth disorders: current insights and therapeutic strategies"],"prefix":"10.3389","volume":"17","author":[{"given":"Zaineb","family":"Sohail","sequence":"first","affiliation":[{"name":"Faculty of Health Sciences, Universiti Sultan Zainal Abidin \u2013 UniSZA","place":["Terengganu, Malaysia"]},{"name":"Department of Life Sciences, School of Science, University of Management and Technology","place":["Lahore, Pakistan"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Norhayati binti 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