HeGRI: A Novel Index of Serum Hepcidin Suppression in Relation to the Degree of Renal Dysfunction among β-Thalassemia Major Patients

<b>Background:</b> The progressive renal function inadequacy results in altered hepcidin metabolism due to a shifting of its renal elimination, which consequently affects enteric iron absorption and iron stores’ availability. This study aimed to investigate and correlate renal function,...

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Main Authors: Burhan A. Zaman, Suzan O. Rasool, Nashwan M. R. Ibrahim, Deldar M. Abdulah
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:Thalassemia Reports
Subjects:
Online Access:https://www.mdpi.com/2039-4365/12/1/2
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author Burhan A. Zaman
Suzan O. Rasool
Nashwan M. R. Ibrahim
Deldar M. Abdulah
author_facet Burhan A. Zaman
Suzan O. Rasool
Nashwan M. R. Ibrahim
Deldar M. Abdulah
author_sort Burhan A. Zaman
collection DOAJ
description <b>Background:</b> The progressive renal function inadequacy results in altered hepcidin metabolism due to a shifting of its renal elimination, which consequently affects enteric iron absorption and iron stores’ availability. This study aimed to investigate and correlate renal function, iron status, and hepcidin in patients with β-thalassemia major through a novel index. <b>Methods:</b> In this 1:1 case–control study, serum hepcidin, serum ferritin, iron study, hematological and renal function parameters were compared between 60 β-thalassemia major patients with iron overload and 61 healthy individuals (2–30 years old). <b>Results:</b> The concentrations of serum hepcidin (21.898 vs. 9.941 ng/mL; <i>p</i> < 0.001) and eGFR (179.71 vs. 132.95; <i>p</i> < 0.001) were significantly higher in β-thalassemia major patients compared to the controls. The serum hepcidin levels decreased with increasing levels of total iron-binding capacity (TIBC; β = −0.442; <i>p</i> = 0.024), transferrin saturation (β = −0.343; <i>p</i> = 0.023), serum creatinine (β = −0.625; <i>p</i> = 0.0030), and eGFR (β = −0.496; <i>p</i> = 0.011). The mean hepcidin/ferritin ratio was significantly lower in the β-thalassemia major cases (0.0069 vs. 0.3970; <i>p</i> < 0.001). The novel hepcidin/eGFR ratio index (HeGRI) was significantly higher in the patient group compared to controls (0.12 vs. 0.09; <i>p</i> = 0.031), respectively. <b>Conclusions:</b> These results suggest that HeGRI could be a potential index of the appropriateness of serum hepcidin suppression associated with the degree of renal dysfunction among β-thalassemia major patients.
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spelling doaj.art-c5801ff23e2d4b22ad1887e2ecaccd782023-11-30T22:37:45ZengMDPI AGThalassemia Reports2039-43652021-12-0112121110.3390/thalassrep12010002HeGRI: A Novel Index of Serum Hepcidin Suppression in Relation to the Degree of Renal Dysfunction among β-Thalassemia Major PatientsBurhan A. Zaman0Suzan O. Rasool1Nashwan M. R. Ibrahim2Deldar M. Abdulah3Department of Basic Sciences, College of Pharmacy, University of Duhok, Duhok City 42001, Kurdistan Region, IraqDepartment of Clinical Pharmacy, College of Pharmacy, University of Duhok, Duhok City 42001, Kurdistan Region, IraqDepartment of Surgery, College of Medicine, University of Duhok, Duhok City 42001, Kurdistan Region, IraqCommunity and Maternity Health Unit, College of Nursing, University of Duhok, Duhok City 42001, Kurdistan Region, Iraq<b>Background:</b> The progressive renal function inadequacy results in altered hepcidin metabolism due to a shifting of its renal elimination, which consequently affects enteric iron absorption and iron stores’ availability. This study aimed to investigate and correlate renal function, iron status, and hepcidin in patients with β-thalassemia major through a novel index. <b>Methods:</b> In this 1:1 case–control study, serum hepcidin, serum ferritin, iron study, hematological and renal function parameters were compared between 60 β-thalassemia major patients with iron overload and 61 healthy individuals (2–30 years old). <b>Results:</b> The concentrations of serum hepcidin (21.898 vs. 9.941 ng/mL; <i>p</i> < 0.001) and eGFR (179.71 vs. 132.95; <i>p</i> < 0.001) were significantly higher in β-thalassemia major patients compared to the controls. The serum hepcidin levels decreased with increasing levels of total iron-binding capacity (TIBC; β = −0.442; <i>p</i> = 0.024), transferrin saturation (β = −0.343; <i>p</i> = 0.023), serum creatinine (β = −0.625; <i>p</i> = 0.0030), and eGFR (β = −0.496; <i>p</i> = 0.011). The mean hepcidin/ferritin ratio was significantly lower in the β-thalassemia major cases (0.0069 vs. 0.3970; <i>p</i> < 0.001). The novel hepcidin/eGFR ratio index (HeGRI) was significantly higher in the patient group compared to controls (0.12 vs. 0.09; <i>p</i> = 0.031), respectively. <b>Conclusions:</b> These results suggest that HeGRI could be a potential index of the appropriateness of serum hepcidin suppression associated with the degree of renal dysfunction among β-thalassemia major patients.https://www.mdpi.com/2039-4365/12/1/2hepcidineGFRrenal dysfunctioniron overloadβ-thalassemia major
spellingShingle Burhan A. Zaman
Suzan O. Rasool
Nashwan M. R. Ibrahim
Deldar M. Abdulah
HeGRI: A Novel Index of Serum Hepcidin Suppression in Relation to the Degree of Renal Dysfunction among β-Thalassemia Major Patients
Thalassemia Reports
hepcidin
eGFR
renal dysfunction
iron overload
β-thalassemia major
title HeGRI: A Novel Index of Serum Hepcidin Suppression in Relation to the Degree of Renal Dysfunction among β-Thalassemia Major Patients
title_full HeGRI: A Novel Index of Serum Hepcidin Suppression in Relation to the Degree of Renal Dysfunction among β-Thalassemia Major Patients
title_fullStr HeGRI: A Novel Index of Serum Hepcidin Suppression in Relation to the Degree of Renal Dysfunction among β-Thalassemia Major Patients
title_full_unstemmed HeGRI: A Novel Index of Serum Hepcidin Suppression in Relation to the Degree of Renal Dysfunction among β-Thalassemia Major Patients
title_short HeGRI: A Novel Index of Serum Hepcidin Suppression in Relation to the Degree of Renal Dysfunction among β-Thalassemia Major Patients
title_sort hegri a novel index of serum hepcidin suppression in relation to the degree of renal dysfunction among β thalassemia major patients
topic hepcidin
eGFR
renal dysfunction
iron overload
β-thalassemia major
url https://www.mdpi.com/2039-4365/12/1/2
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