Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid

In order to investigate the effect of folate depletion, lymphocyte sister-chromatid exchange (SCE) rates were compared among homozygous β-thalassaemic patients with low folic acid levels, heterozygous β-thalassaemic patients with normal folate levels and healthy persons with normal haemoglobin, in cultures with both normal and depleted folate conditions. Significantly higher SCE rates were found in homozygous patients in all assays, but the in vitro folate depletion did not induce an increase in SCE frequency in any group.

Keywords

β-Thalassaemia, Culture conditions, Follic acid, Sister-chromatid exchange, folic acid, beta thalassemia, clinical article, controlled study, heterozygote, homozygote, human, human cell, lymphocyte culture, priority journal, sister chromatid exchange, Adolescent, Adult, Analysis of Variance, Cells, Cultured, Child, Child, Preschool, Folic Acid Deficiency, Human, Infant, Lymphocytes, Sister Chromatid Exchange, Support, Non-U.S. Gov't, Thalassemia