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Role of SLC40A1 R-178G Gene Mutation on Pathophysiology of Iron Deficient Sickle Cell Anemia Patients


Affiliations
1 Department of Pediatrics, Shyam Shah Medical College, Rewa, MP, India
2 Department of Zoology, Govt. Girl PG College, MP, India
3 Department. of Anesthesiology, Shyam Shah Medical College, Rewa, MP, India
4 Department of Biotechnology, Guru Ghasidas University, Bilashpur (CG), India
5 Multidisciplinary Research Unit, Shyam Shah Medical College, Rewa, MP, India
     

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Introduction: Solute carrier family 40 member 1(SLC40A1) is a protein coding gene. The protein encoded by this gene is a cell membrane protein that plays a key role in the majority of iron transportation by balancing cellular and systemic iron levels. Defects in this gene are a cause of hemochromatosis type 4 (HFE4) and Hemochromatosis type 1 diseases. Ironoverload and a non-responsive phenotype are also associated with the hereditary variants of iron deficiency anemia. Based on this, it was proposed that the presence of this mutation could influence iron absorption and provide protection against the severity of iron deficiency in sickle syndrome. SLC40A1 gene mutations may have a useful clinical result in the severity of the disease due to their diverse role in iron metabolism.

Materials & Methods: A total of 140 iron-deficient sickle syndrome patients were recruited for the study with an equal number for controls. The sickle cell sub-type was diagnosed by a cation exchange high performance liquid chromatography (HPLC) and complete blood count analysis was done by automated hematoanalyzer. Screening of iron deficiency was done by serum ferritin analysis using ELISA method. Genomic DNA was isolated from peripheral blood by kit method and DNA quantification was done by Nano drop analytical Software system. SLC40A1 R178G genotype analysis was performed by PCR-RFLP method using HpyAV restriction enzyme.

Results: Among the Sickle cell disease (SCD) patients, 17 were heterozygous and 09 were homozygous for SLC40A1(R178G) mutation; while 13 controls were heterozygous and 5 patients were homozygous for SLC40A1(R178G) mutation. We reported the significant elevation of serum ferritin and hemoglobin level in SLC40A1(R178G) mutation while a decrease in the ESR and CRP levels were observed.

Conclusion: The findings of the study suggested high impact of SLC40A1(R178G) mutation in pathophysiology of iron deficient SCD and shows positive correlation. It may act as the predictor of disease severity. Detection of this mutation in iron-deficient SCD patients is useful in treatment decision.

Based on this finding, clinicians can be more confident about iron status in SCD patients. Data from this research can be used to understand the status of iron overload in mutant versus non-mutant conditions. The Data of the study provides a genotype–phenotype correlation of SLC40A1 (R178G) mutation in iron-deficient SCD patients.



Keywords

PCR, RFLP, SCD, IDA, SLC40A1, SNP
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  • Role of SLC40A1 R-178G Gene Mutation on Pathophysiology of Iron Deficient Sickle Cell Anemia Patients

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Authors

Sweta Pandey
Department of Pediatrics, Shyam Shah Medical College, Rewa, MP, India
Shalini Kunder
Department of Zoology, Govt. Girl PG College, MP, India
Naresh Bajaj
Department of Pediatrics, Shyam Shah Medical College, Rewa, MP, India
Sudhakar Dwivedi
Department. of Anesthesiology, Shyam Shah Medical College, Rewa, MP, India
Vibha Singh
Department of Biotechnology, Guru Ghasidas University, Bilashpur (CG), India
Sanjay Kumar Pandey
Multidisciplinary Research Unit, Shyam Shah Medical College, Rewa, MP, India

Abstract


Introduction: Solute carrier family 40 member 1(SLC40A1) is a protein coding gene. The protein encoded by this gene is a cell membrane protein that plays a key role in the majority of iron transportation by balancing cellular and systemic iron levels. Defects in this gene are a cause of hemochromatosis type 4 (HFE4) and Hemochromatosis type 1 diseases. Ironoverload and a non-responsive phenotype are also associated with the hereditary variants of iron deficiency anemia. Based on this, it was proposed that the presence of this mutation could influence iron absorption and provide protection against the severity of iron deficiency in sickle syndrome. SLC40A1 gene mutations may have a useful clinical result in the severity of the disease due to their diverse role in iron metabolism.

Materials & Methods: A total of 140 iron-deficient sickle syndrome patients were recruited for the study with an equal number for controls. The sickle cell sub-type was diagnosed by a cation exchange high performance liquid chromatography (HPLC) and complete blood count analysis was done by automated hematoanalyzer. Screening of iron deficiency was done by serum ferritin analysis using ELISA method. Genomic DNA was isolated from peripheral blood by kit method and DNA quantification was done by Nano drop analytical Software system. SLC40A1 R178G genotype analysis was performed by PCR-RFLP method using HpyAV restriction enzyme.

Results: Among the Sickle cell disease (SCD) patients, 17 were heterozygous and 09 were homozygous for SLC40A1(R178G) mutation; while 13 controls were heterozygous and 5 patients were homozygous for SLC40A1(R178G) mutation. We reported the significant elevation of serum ferritin and hemoglobin level in SLC40A1(R178G) mutation while a decrease in the ESR and CRP levels were observed.

Conclusion: The findings of the study suggested high impact of SLC40A1(R178G) mutation in pathophysiology of iron deficient SCD and shows positive correlation. It may act as the predictor of disease severity. Detection of this mutation in iron-deficient SCD patients is useful in treatment decision.

Based on this finding, clinicians can be more confident about iron status in SCD patients. Data from this research can be used to understand the status of iron overload in mutant versus non-mutant conditions. The Data of the study provides a genotype–phenotype correlation of SLC40A1 (R178G) mutation in iron-deficient SCD patients.



Keywords


PCR, RFLP, SCD, IDA, SLC40A1, SNP

References