Abstract

Iron deposition in various organs can cause endocrine complications in patients with transfusion-dependent beta-thalassemia. The aim was to investigate the relationship between endocrine complications and pancreatic iron overload using magnetic resonance imaging (MRI). Forty patients with transfusion-dependent thalassemia (TDT) were enrolled in the study. The magnetic resonance imagings of the patients were performed using a 1.5 Tesla Philips MRI scanner. Two out of three patients had at least one clinical endocrine complication. The rate of iron deposition was 62.5% in liver, and 45% in pancreas tissue, and was 12.5% in heart tissue. Pancreatic T2* and hepatic T2* values were significantly positively correlated (p = 0.006). Pancreatic T2* and ferritin were significantly negatively correlated (p = 0.03). Cardiac T2* values were negatively correlated with fasting blood glucose (p = 0.03). Patients with short stature had significantly higher cardiac iron burden (22.3 vs. 36.6 T2*ms; p 0.01), and patients with hypothyroidism had higher liver iron concentrations (9.9 vs. 6.4 LIC mg/g; p = 0.05). The ferritin level of 841ng/mL and liver iron concentration (LIC) value of 8.7mg/g were detected as the threshold level for severe pancreatic iron burden (AUC 70%, p:0.04, AUC 80%, p = 0.002, respectively). Moreover, males were found to have decreased pancreas T2* values compared with the values in females (T2* 19.3 vs. 29.9, p = 0.05). Patients with higher ferritin levels over than 840ng/mL should be closely monitored for pancreatic iron deposition, and patients with endocrine complications should be assessed in terms of cardiac iron burden.

Highlights

  • Transfusion-dependent thalassemia (TDT) requires regular blood transfusions, and the iron overload is unavoidable if chelation therapy is not suitable [1]

  • Iron can deposit in extrahepatic organs such as heart and pancreas in the form of non– transferrin-bound iron (NTBI) [4]

  • The serum ferritin level of 841 ng/mL was detected as the threshold level for liver iron deposition with 80% sensitivity and 80% specificity (p = 0.002, AUC = 0.80) and was determined as the threshold level for severe pancreatic iron burden with 83% sensitivity and 54% specificity (p = 0.04, AUC = 0.70)

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Summary

Introduction

Transfusion-dependent thalassemia (TDT) requires regular blood transfusions, and the iron overload is unavoidable if chelation therapy is not suitable [1]. Iron can deposit in extrahepatic organs such as heart and pancreas in the form of non– transferrin-bound iron (NTBI) [4]. These organs are sensitive to chelation therapy [5]. Screening the association of iron burden in extrahepatic organs is one another way of evaluation for patients Studies supporting these assumptions showed that iron overload in endocrine organs can have association with hepatic and cardiac functions [6, 7]. We aimed to screen the endocrine comorbidities of TDT patients, and to investigate the relationship between comorbidities and iron overload in pancreas, liver, and heart

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