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Updated: Nov 6, 2025

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
A double-blind, controlled, crossover trial of amlodipine on iron overload status in transfusion dependent
Hossein Karami1, Hadiseh Khalilzadeh Arjmandi2, Ebrahim Salehifar3
1Thalassemia Research Center (TRC), Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.
Insights
Amlodipine may reduce iron overload in transfusion-dependent beta-thalassemia patients. This study showed amlodipine improved myocardial T2* and serum ferritin levels compared to placebo.
Area of Science:
- Cardiology
- Hematology
- Pharmacology
Background:
- Transfusion-dependent beta-thalassemia (TDT) leads to iron overload.
- Myocardial iron loading is a significant complication in TDT patients.
- Effective strategies to manage iron overload in TDT are crucial.
Purpose of the Study:
- To investigate the efficacy of amlodipine in improving myocardial iron loading in TDT patients.
- To assess amlodipine's effect on serum ferritin levels.
- To compare amlodipine's impact against a placebo in a crossover study design.
Main Methods:
- A placebo-controlled, crossover study involving 19 TDT patients.
- Patients received amlodipine (5 mg daily) or placebo for 6 months, followed by a 2-week washout.
- Efficacy was measured using myocardial T2*-weighted MRI (magnetic resonance imaging) and serum ferritin levels.
Main Results:
- Amlodipine treatment increased myocardial MRI T2* values from a baseline of 9.83 ± 2.67 ms to 11.44 ± 4.14 ms.
- Placebo treatment resulted in a smaller increase in myocardial MRI T2* to 10.29 ± 4.01 ms.
- Amlodipine demonstrated a significant improvement in both myocardial MRI T2* and serum ferritin levels compared to placebo.
Conclusions:
- Amlodipine shows potential in improving myocardial iron loading and reducing serum ferritin in TDT patients.
- The findings suggest amlodipine as a possible therapeutic option for managing iron overload in TDT.
- Larger clinical trials are recommended to validate these preliminary results.
Background And Aim:
This study examined whether administration of amlodipine could improve myocardial iron loading status in patients with transfusion dependent β-thalassemia (TDT), through a placebo-controlled, crossover study.
Methods:
Amlodipine (5 mg, daily) or placebo were prescribed to all patients (n = 19) for 6 months, and after a 2-week washout period, patients were crossed over to the other group. The efficacy of amlodipine on iron loading was assessed by measuring myocardial T2*-weighted magnetic resonance imaging (MRI T2*, millisecond [ms]) and serum ferritin (ng/mL).
Results:
Seventeen patients completed the study. The mean ± standard deviation [SD] of myocardial MRI T2* at baseline was 9.83 ± 2.67 ms Myocardial MRI T2* value rose to 11.44 ± 4.14 ms post amlodipine treatment in all patients. After placebo, myocardial MRI T2* value reached 10.29 ± 4.01 ms After controlling the baseline measures, Hedges's g for ferritin and myocardial MRI T2* outcomes were estimated 3.84 (95% confidence interval [CI] 2.68 to 4.97) and -1.80 (95% CI -2.58 to -0.10), respectively.
Conclusion:
Amlodipine might improve myocardial MRI T2* and serum ferritin level compared to placebo. However, larger clinical studies are needed to confirm the results.
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