Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017 Apr 1;11(2):133-138.

Renal Hemosiderosis among Iranian Transfusion Dependent β-Thalassemia Major Patients

Affiliations

Renal Hemosiderosis among Iranian Transfusion Dependent β-Thalassemia Major Patients

Mozhgan Hashemieh et al. Int J Hematol Oncol Stem Cell Res. .

Abstract

Background: In recent years, the success in management of thalassemic patients, has allowed for some previously unrecognized complications including renal abnormalities to emerge. This prospective study aimed to investigate kidney iron overload by means of MRI T2* and also renal function based on laboratory tests for early markers of glomerular and tubular dysfunction among adult Iranian transfusion-dependent thalassemia major patients. Subjects and Methods: Two-hundred and two patients with transfusion-dependent β-thalassemia major were included in this study in Zafar Adult Thalassemia Center, Tehran, Iran. For all patients, kidney MRI T2* as well as evaluation of BUN, creatinine, uric acid, calcium, phosphorus, sodium (Na), potassium (K), total protein, albumin, cystatin C, serum ferritin β2-microglobulin, NAG (N-acetyl-beta-D-Glucosaminidase), and urine protein were performed. Results: One-hundred and fourteen female and 88 male transfusion-dependent β-thalassemia major patients with mean age of 30.1 ± 9.4 participated in the present study. We found that 77.7% of our patients had kidney hemosiderosis based on MRI T2*. Also, 67 patients (33.2%) had elevation of serum cystatin C, and 104 patients (51.5%) had reduced estimated glomerular filtration rate (e-GFR). Increased urinary excretion of NAG and hypercalciuria were found in 50% and 79.2% of participants, respectively. Conclusion: Renal hemosiderosis and asymptomatic renal dysfunction are prevalent among transfusion- dependent β-thalassemia major patients which necessitate regular screening with early markers of glomerular and tubular dysfunction. Further studies in order to investigate the correlation between renal hemosiderosis and early markers of kidney dysfunction among these patients are recommended.

Keywords: Iran; MRI T2*; Renal involvement; Transfusion; β-Thalassemia major.

PubMed Disclaimer

References

    1. Weatherall DJ. The inherited diseases of hemoglobin are an emerging global health burden. Blood. 2010;115(22):4331–6. - PMC - PubMed
    1. Cunningham MJ, Sankaran VG, Nathan DG, et al. The thalassemia syndromes. In: Orkin SH, Nathan DG, Ginsburg D, Fisher DE, Look AT, Lux SE, editors. Nathan and Oski’s Hematology of Infancy and Childhood. 7th ed. Saunders: 2009. pp. 1015–76.
    1. Bakr A, Al-Tonbary Y, Osman G, et al. Renal complications of beta-thalassemia major in children. Am J Blood Res. 2014;4(1):1–6. - PMC - PubMed
    1. Azarkeivan A, Hashemieh M, Akhlaghpoor S, et al. Relation between serum ferritin and liver and heart MRI T2* in beta thalassaemia major patients. East Mediterr Health J. 2013;19(8):727–32. - PubMed
    1. Hashemieh M, Azarkeivan A, Akhlaghpoor S, et al. T2-star (T2*) magnetic resonance imaging for assessment of kidney iron overload in thalassemic patients. Arch Iran Med. 2012;15(2):91–4. - PubMed