Open AccessEffect of the Hemochromatosis Mutations on Iron Overload among the Indian β Thalassemia Carriers
Author(s) -
Nadkarni Anita H.,
Singh Aradhana A.,
Colaco Stacy,
Hariharan Priya,
Colah Roshan B.,
Ghosh Kanjaksha
Publication year - 2017
Publication title -
journal of clinical laboratory analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 50
eISSN - 1098-2825
pISSN - 0887-8013
DOI - 10.1002/jcla.22054
Subject(s) - hemochromatosis , hereditary hemochromatosis , genotype , allele , ferritin , thalassemia , genetics , mutation , haplotype , medicine , biology , gene
Background Hereditary hemochromatosis is a disorder of iron metabolism characterized by increased iron absorption. HFE gene mutations C282Y and H63D are responsible for the majority of hereditary hemochromatosis cases. Methods We tried to look at the effect of HFE mutations on the iron status. A total of 100 β thalassemia traits ( BTT ) with 100 normal individuals were screened for the C282Y and H63D mutations using PCR ‐ RFLP . The serum ferritin levels were determined using ELISA kit. Results We did not find the C282Y mutation in our study group. The allelic frequencies for H63D mutation did not differ significantly between β‐thalassemia traits (8.5%) and normal controls (9%). ΒΤΤ with H63D genotype of H/D (143.16 ± 80.3 ng/ml) and D/D (504 ng/ml) showed higher ferritin levels as against H/H genotype (88.64 ± 92.43 ng/ml). The statistically significant difference was observed in the mean serum ferritin levels among the individuals showing H/H and D/D genotypes ( P < 0.002) and H/D and D/D genotype ( P < 0.01) in both the groups. Conclusion This suggests that iron load in BTT tends to aggravated with the co‐inheritance of the H63D mutation. The mutant H63D gene showed the presence of haplotype 6 which is reported in the European population suggesting a common origin.