Published online Sep 20, 2026. doi: 10.5493/wjem.120531
Revised: April 9, 2026
Accepted: June 4, 2026
Published online: September 20, 2026
Processing time: 203 Days and 13.9 Hours
Osteoclastic bone diseases represent a significant health burden, especially in an aging population, due to imbalances in bone homeostasis that result in postmenopausal osteoporosis, inflammatory arthritis, malignancy-induced bone disease and secondary metabolic conditions, which result in fragility fractures, disability and death. Although advances in imaging and pharmacology have enhanced management, existing diagnostic strategies have poor sensitivity in detecting early-stage pathological changes or fracture risk. The NF-kappaB/receptor activator of NF-kappaB ligand (RANKL)/osteoprotegerin (OPG) pathway is important in bone turnover regulation, which is dysregulated in bone degradation, leading to increased os
Core Tip: The receptor activator of NF-kappaB/receptor activator of NF-kappaB ligand (RANKL)/osteoprotegerin (OPG) pathway is a pivotal bone remodeling pathway, and its disruption is responsible for osteoclast-driven bone resorption in osteoporosis, arthritis and bone-related cancer. Plasma RANKL and OPG, and their ratio, may be more sensitive indicators for diagnosis, fracture prediction and therapy assessment. While assays are variable, there is evidence that the RANKL/OPG ratio could be a better predictor than either marker alone, with potential to improve diagnosis, treatment and outcomes in bone resorption disease.