Assessment of Serum Vitamin D, Ferritin and Bone Age in Children with Beta Thalassemia
Ira Devi Alamsyah Guntoro, Wulandewi Marhaeni, Alfi Yasmina, Ari Yunanto, Arief Budiarto
Asian Journal of Medicine and Health · pp. 66–77 · Published 9 Dec 2025
10.9734/ajmah/2025/v23i121333Abstract
Background: Vitamin D deficiency is a common condition that occurs in children with beta thalassemia with a multifactorial aetiology. Excess iron in the liver, skin, parathyroid, and endocrine organs (pituitary) is studied as a cause of vitamin D deficiency in beta thalassemia patients. Literature showed that serum ferritin levels were significantly negatively correlated with vitamin D levels. Aims: The primary purpose of the study is to determine the correlation between vitamin D serum and delayed bone age with serum ferritin level in children with beta thalassemia. Study Design: A cross-sectional study was conducted to evaluate the serum levels of vitamin D, ferritin, and bone age in children diagnosed with beta thalassemia. Place and Duration of Study: The study was conducted at the Pediatric Haematology and Oncology outpatient clinic and inpatient ward, Ulin General Hospital, Banjarmasin, South Kalimantan, Indonesia, between January 2024 and March 2024. Methodology: The study included 55 patients (34 male, 21 female; age range 2-18 years) with beta thalassemia, who underwent outpatient and inpatient treatment. Ferritin serum, 25-OH vitamin D level, and bone age were measured on the day of treatment. Bivariate analysis used the Spearman correlation test, with results considered significant if p<0.05. Results: Out of 55 patients, 50 patients (90,9%) experienced vitamin D insufficiency/deficiency and 15 patients (27.3%) experienced delayed bone age. There was a very weak and not significant correlation between serum ferritin level and serum vitamin D 25-OH level (r=-0.12; p=0.38), also between serum ferritin level and delayed bone age (r= 0.09; p=0.51). Conclusion: There is no correlation between serum ferritin level and vitamin D level, nor delayed bone age in children with beta thalassemia.
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