Literature DB >> 19737308

Absence of cardiac siderosis by MRI T2* despite transfusion burden, hepatic and serum iron overload in Lebanese patients with sickle cell disease.

Adlette Inati1, Khaled M Musallam, John C Wood, Marwan Sheikh-Taha, Linda Daou, Ali T Taher.   

Abstract

BACKGROUND: The use of magnetic resonance imaging (MRI) to detect organ-specific iron overload is becoming increasingly common. Although hepatic iron overload has been recognized in patients with sickle cell disease (SCD), cardiac iron deposition has only been examined in a few reports.
METHODS: This was a cross-sectional study of 23 patients with SCD. Patient charts were reviewed and data collected for drug use, total lifetime transfusions (TLT), transfusion rate (TR), status of the spleen, and comorbid illnesses or infections. Blood samples were obtained for assessment of hemoglobin, serum ferritin, non-transferrin-bound iron (NTBI), and liver enzyme levels. Doppler echocardiography was performed to detect pulmonary hypertension (PHT) and assess left ventricular ejection fraction. Cardiac iron levels were measured by MRI T2*. Direct determination of liver iron concentration (LIC) was performed using R2 MRI. In this study, cardiac T2* >20 ms was considered normal.
RESULTS: The mean age was 24.4 +/- 9.7 yr, with a male to female ratio of 15:8. A total of 9 (49.9%) patients were splenectomized. The mean TR was 14.1 +/- 13.2 Units/yr, and the mean hemoglobin level was 9.0 g/dL. PHT was detected in 6 (27.3%) patients, but none had evidence of heart failure. The mean serum ferritin, LIC, and NTBI levels were 997.7 ng/mL, 4.6 mg Fe/g dw, and 1.1 +/- 2.2, respectively. TR was a much better predictor of iron burden (LIC, ferritin, NTBI) than TLT. In fact, TR less than 10 Units/yr did not produce significant iron overload reflecting spontaneous losses as high as 0.11 mg/kg/d. None of the patients had evidence of cardiac iron overload (mean cardiac T2* = 37.3 +/- 6.2 ms; range: 21.9-46.8 ms). There was also no statistically significant correlation between cardiac T2* values and any of the study variables.
CONCLUSION: Our study demonstrates that TR is a stronger predictor of iron overload than TLT. It also confirms cardiac sparing in patients with SCD, even in subjects with significant transfusion burden, systemic and hepatic iron overload.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19737308     DOI: 10.1111/j.1600-0609.2009.01345.x

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  10 in total

1.  Extramedullary haematopoiesis correlates with genotype and absence of cardiac iron overload in polytransfused adults with thalassaemia.

Authors:  Paolo Ricchi; Massimiliano Ammirabile; Anna Spasiano; Silvia Costantini; Tiziana Di Matola; Alessia Pepe; Patrizia Cinque; Leonilde Pagano; Maddalena Casale; Aldo Filosa; Luciano Prossomariti
Journal:  Blood Transfus       Date:  2013-10-03       Impact factor: 3.443

Review 2.  Cardiovascular abnormalities in sickle cell disease.

Authors:  Mark T Gladwin; Vandana Sachdev
Journal:  J Am Coll Cardiol       Date:  2012-03-27       Impact factor: 24.094

3.  Automated T(2) * measurements using supplementary field mapping to assess cardiac iron content.

Authors:  Brian A Taylor; Ralf B Loeffler; Ruitian Song; Mary E McCarville; Jane S Hankins; Claudia M Hillenbrand
Journal:  J Magn Reson Imaging       Date:  2013-01-04       Impact factor: 4.813

Review 4.  How we manage iron overload in sickle cell patients.

Authors:  Thomas D Coates; John C Wood
Journal:  Br J Haematol       Date:  2017-03-14       Impact factor: 6.998

5.  Right and left ventricular function and myocardial scarring in adult patients with sickle cell disease: a comprehensive magnetic resonance assessment of hepatic and myocardial iron overload.

Authors:  Flávia P Junqueira; Juliano L Fernandes; Guilherme M Cunha; Tadeu T A Kubo; Claudio M A O Lima; Daniel B P Lima; Marly Uellendhal; Sidney R Sales; Carolina A S Cunha; Viviani L R de Pessoa; Clarisse L C Lobo; Edson Marchiori
Journal:  J Cardiovasc Magn Reson       Date:  2013-09-19       Impact factor: 5.364

6.  Electrocardiographic Study in Adult Homozygous Sickle Cell Disease Patients in Lagos, Nigeria.

Authors:  Adedoyin Dosunmu; Akinsegun Akinbami; Ebele Uche; Adewumi Adediran; Sarah John-Olabode
Journal:  J Trop Med       Date:  2016-09-21

Review 7.  MRI Measurements of Iron Load in Transfusion-Dependent Patients: Implementation, Challenges, and Pitfalls.

Authors:  Charles T Quinn; Tim G St Pierre
Journal:  Pediatr Blood Cancer       Date:  2015-12-29       Impact factor: 3.167

Review 8.  Iron overload disorders.

Authors:  Christine C Hsu; Nizar H Senussi; Kleber Y Fertrin; Kris V Kowdley
Journal:  Hepatol Commun       Date:  2022-06-14

9.  The role of MRI-R2* in the detection of subclinical pancreatic iron loading among transfusion-dependent sickle cell disease patients and correlation with hepatic and cardiac iron loading.

Authors:  Basant Mohamed Raief Mosaad; Ahmed Samir Ibrahim; Mohamed G Mansour; Mohsen Saleh ElAlfy; Fatma Soliman Elsayed Ebeid; Emad H Abdeldayem
Journal:  Insights Imaging       Date:  2022-09-04

10.  Statural Growth and Prevalence of Endocrinopathies in Relation to Liver Iron Content (LIC) in Adult Patients with Beta Thalassemia Major (BTM) and Sickle Cell Disease (SCD).

Authors:  Mohamed A Yassin; Ashraf T Soliman; Vincenzo De Sanctis; Mohammad A J Abdula; Lubna M Riaz; Firdous F Ghori; Anil Yousaf; Abdulqadir J Nashwan; Sandara Abusamaan; Abbas Moustafa; Samah Kohla; Dina S Soliman
Journal:  Acta Biomed       Date:  2018-02-16
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.