To the editor Osteoporosis in children with chronic diseases has long been recognized as a major endocrine complication during the preand posttreatment periods, possibly triggered by the disease itself or its treatment. Despite advanced and targeted management of childhood illnesses, the use of systemic glucocorticoids (GC) remains the cornerstone of treatment for various acute and chronic conditions, including infections, cancers, autoimmune disorders, respiratory distress, and neuromuscular disorders. 1) However, bone mass, shape, and bone metabolic status continue to significantly change during childhood and adolescence; thus, children are more sensitive to the detrimental effects of GC use because it exerts both direct and indirect adverse effects on the growth plate and developing skeleton, causing chondrocyte apoptosis, premature osteocyte death, and excessive bone resorption via prolongation of osteoclast survival. 1) Although age upon starting GC and its duration of use are major osteo toxic contributors, spontaneous recovery of bone mass follow ing treatment completion is a privilege of this specific age group. 2) Nevertheless, the extent of bone mass recovery after the cessation of therapy remains unknown. According to the International Society for Clinical Densitometry, pediatric osteoporosis is diagnosed when nontraumatic vertebral fracture (VF) is con firmed or, in the absence of VF, a clinically significant fracture history along with a bone mineral density (BMD) z score of less than -2.0 is measured by dual-energy x-ray absorptiometry (DXA). 3) Unfortunately, measuring BMD using DXA in younger children is challenging, and nontraumatic VF is easily overlooked due to its asymptomatic nature and normal BMD. 4) A Canadian multicenter observational cohort study determined the severity of the underlying disease, average daily and cumulative dose of GC, and duration of therapy (highest at 12 months of therapy) as predictive factors of incidental VF. 5) Although longitudinal cohorts from a large-scale population yield the most reliable results, Kuniyil et al. 6) presented a distinct study design that investigated the effect of GC on pediatric BMD for a short treatment period.This study highlights the detrimental effects of systemic GC use on pediatric BMD. DXA-interpreted BMD data (wholebody, lumbar spine, nondominant distal radius, and total body less head) of 25 patients with heterogeneous diseases (21 with tuberculosis, 2 with juvenile idiopathic arthritis, 1 with inflammatory bowel disease, and 1 with autoimmune hemolytic