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Biol."],"abstract":"<jats:p>Ferroptosis, an iron-dependent form of regulated cell death characterized by lipid peroxidation, has emerged as a pivotal mechanism in bone disorders including osteoporosis and osteonecrosis. The nuclear factor erythroid 2\u2013related factor 2 (Nrf2)\/heme oxygenase-1 (HO-1) signaling axis plays a paradoxical role\u2014contributing to cytoprotection under oxidative stress, yet potentially promoting ferroptosis through excessive iron accumulation. This review summarizes how the Nrf2\/HO-1 pathway modulates ferroptosis across osteoblasts, osteoclasts, and osteocytes, and its impact on bone homeostasis. We explore the pathway\u2019s involvement in the shift from physiological bone remodeling to pathological bone loss. Given its dual role, the Nrf2\/HO-1 axis represents both a challenge and an opportunity for therapeutic intervention. 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