Vitamin C Deficiency and Oxidant Levels in Children With Transfusion-Dependent β-Thalassemia

Objectives To study vitamin C levels in children with transfusion-dependent β-thalassemia and correlate with age, transfusions received and iron overload; and to study the effect of administering vitamin C on its levels and Malondialdehyde (MDA) in deficient patients. Methods This case-control study enrolled 100 children with transfusion-dependent β-thalassemia and 30 healthy controls. MDA levels before and after administration of vitamin C were performed randomly in 36 children with low vitamin C levels. Results 81/95 (85.3%) study subjects vs none in control group, had low plasma vitamin C levels ( P <0.001). Vitamin C levels were low in 64 of 71 (74.7%) subjects with dietary deficiency, while none of the 19 (63.3%) controls with dietary deficiency had low levels ( P =0.04). Increasing serum ferritin values correlated with vitamin C deficiency ( P =0.02). The mean level of MDA reduced ( P <0.001) with vitamin C supplementation. Conclusions Low levels of vitamin C are common in children with thalassemia. Dietary counseling along with supplementation with vitamin C, in those with low levels may prevent oxidative stress.