Pediatric Sciences Journal | 2021

Detoxification Genomics in Children with β-Thalassemia Major: Pilot Study of Glutathione S Transferase M1, Pi & Methyltetrahydrofolate Reductase Gene Polymorphisms Combinations in β- Thalassemia Major

 
 
 
 
 
 
 
 

Abstract


Background:\xa0Children with β-thalassemia major differ regarding age at presentation, transfusion requirements and unpredictable timing, rate and severity of hemolytic crisis. The blood transfusions are associated with iron overload.\xa0\xa0Glutathione S transferase M1 (GSTM1) null mutation was reported to be associated with myocardial iron overload with low body iron.\xa0 Aim of the Work:\xa0To investigate if children with β-thalassemia major have more than a detoxification enzyme defect. Materials and Methods:\xa0GSTM1, glutathione S transferase Pi (GSTPi)\xa0and methyltetrahydrofolate reductase\xa0(MTHFR)\xa0polymorphism were studied among 97 children with β-thalassemia major\xa0in a cross-sectional study. Results:\xa0The studied cohort comprised 24 (24.7%) girls and 73 (75.3%) boys. Mean hemoglobin was 5.9+/- 0.7gm%, serum iron was 145.69 +/- 58.6 mcg% and total iron binding capacity was 222.58 +/-50.66 mcg%. Of them, 68 (70.1%) demonstrated single or multiple polymorphisms (43 had\xa0GSTM1, 20\xa0GSTPi\xa0and 32 with\xa0MTHFR\xa0polymorphisms respectively), while 29 (29.2%) did not demonstrate any polymorphism. There was no correlation between type, number of polymorphisms and clinical phenotype. Sample size and cross- sectional nature of our study did not allow genotype-phenotype correlation. Most of studied children express\xa0GSTM1, GSTPi and MTHFR\xa0gene polymorphism which was not consistent among them.\xa0 Conclusion:\xa0Children with β-thalassemia major may have one or more than a detoxification/ regeneration potential enzyme gene\xa0GSTM1, GSTPi and MTHFR\xa0polymorphism. Every child with β-thalassemia major has unique genetic detoxification and regeneration abilities. The detected detoxification defects might explain the lack of predictability of occurrence of hemolytic attacks and their severity. More studies are needed to highlight impact of detoxification and regeneration genomics in β-thalassemia.

Volume None
Pages None
DOI 10.21608/cupsj.2021.55630.1011
Language English
Journal Pediatric Sciences Journal

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