Abstract
Sjögren's syndrome (SS) is a systemic autoimmune disorder predominantly affecting middle-aged and elderly women, characterized by lymphocytic infiltration of exocrine glands-particularly the salivary and lacrimal glands-resulting in xerophthalmia and xerostomia. Osteoporosis (OP), sharing similar age of onset and gender predilection, is a skeletal disorder defined by reduced bone mineral density and heightened fracture risk. The comorbidity of SS and OP represents a prevalent clinical phenomenon, with studies reporting an incidence rate of 33.1% to 51.6% among SS patients, significantly higher than that observed in healthy elderly populations. Vitamin D metabolism, widespread abnormal immune responses, hormonal imbalances, metabolic acidosis, and the RANKL/RANK/OPG axis exert significant contributory roles in the pathogenesis of both conditions. Treatment regimens for SS and OP may present certain overlaps yet potential contradictions. In this narrative review, we summarize the bidirectional relationship between these two diseases, thoroughly discuss the existing challenges in their management, and emphasize that recommending a comprehensive management strategy for SS patients with concurrent OP is crucial for enhancing patients' quality of life.