Literature DB >> 26818147

Real-life experience with liver iron concentration R2 MRI measurement in patients with hemoglobinopathies: baseline data from LICNET.

Angela Vitrano1, Giuseppina Calvaruso1, Lorenzo Tesé1, Francesco Gioia1, Filippo Cassarà1, Saveria Campisi2, Franco Butera2, Valeria Commendatore2, Michele Rizzo3, Vincenzo Santoro3, Valeria Cigna4, Alessandra Quota5, Sabrina Bagnato5, Crocetta Argento6, Carmelo Fidone7, Dario Schembari7, Calogera Gerardi8, Filippo Barbiera8, Giuseppe Bellisssima9, Giovanni Giugno9, Gesualdo Polizzi10, Rosamaria Rosso10, Giovanna Abbate11, Vincenzo Caruso11, Elisabetta Chiodi12, Maria Rita Gamberini12, Benedetta Giorgi13, Maria Caterina Putti13, Aldo Filosa14, Maria Rosaria De Ritis14, Esther Oliva15, Nicola Arcadi15, Maria Fustaneo1, Laura Mistretta1, Rosario Di Maggio1, Massimiliano Sacco1, Di Salvo Veronica1, Antonino Giangreco1, Aurelio Maggio16.   

Abstract

BACKGROUND: Real-life data on the use of R2 MRI for the assessment of liver iron concentration (LIC) remain limited.
METHODS: We conducted a cross-sectional analysis on 363 patients (mean age 35.6 yr, 44.1% men) with hemoglobinopathies (204 β-thalassemia major [TM], 102 β-thalassemia intermedia [TI], and 57 sickle cell disease [SCD]) that were evaluated with R2 MRI as part of LICNET, an MRI network of 13 Italian treatment centers.
RESULTS: The mean LIC was 7.8 mg/g (median: 4.0), with high LIC (>7 mg/g) noted in both transfused (TM, TI 37%; SCD 38%) and non-transfused (TI 20%) patients. Ferritin levels correlated with LIC in both transfused (TM, TI, SCD) and non-transfused (TI) patients (P < 0.001), although lower values predicted high LIC in non-transfused patients (1900 vs. 650 ng/mL in TM vs. non-transfused TI). A correlation between LIC and ALT levels was only noted in HCV-negative patients (rs = 0.316, P < 0.001). The proportion of patients with high LIC was significantly different between iron chelators used (P = 0.023), with the lowest proportion in deferasirox (30%) and highest in deferiprone (53%)-treated patients.
CONCLUSIONS: High LIC values persist in subgroups of patients with hemoglobinopathy, warranting closer monitoring and management optimization, even for non-transfused patients with relatively low ferritin levels.
© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  diagnosis; iron overload; sickle cell disease; thalassemia

Mesh:

Substances:

Year:  2016        PMID: 26818147     DOI: 10.1111/ejh.12740

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


  4 in total

Review 1.  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

2.  Iron Chelation Reduces DNA Damage in Sickle Cell Anemia.

Authors:  Rawan S Al-Khateeb; Hanan S Althagafy; Mohammad Zaki ElAssouli; Dunya A Nori; Mohammed AlFattani; Salwa A Al-Najjar; Turki Al Amri; Anwar M Hashem; Steve Harakeh; Nawal Helmi
Journal:  Clin Appl Thromb Hemost       Date:  2021 Jan-Dec       Impact factor: 2.389

Review 3.  Hepatocellular carcinoma in adult thalassemia patients: an expert opinion based on current evidence.

Authors:  Alessandra Mangia; Davide Bellini; Umberto Cillo; Andrea Laghi; Giuseppe Pelle; Vanna Maria Valori; Eugenio Caturelli
Journal:  BMC Gastroenterol       Date:  2020-08-03       Impact factor: 3.067

4.  Iron overload in patients with rare hereditary hemolytic anemia: Evidence-based suggestion on whom and how to screen.

Authors:  Stephanie van Straaten; Bart J Biemond; Jean-Louis Kerkhoffs; Jerney Gitz-Francois; Richard van Wijk; Eduard J van Beers
Journal:  Am J Hematol       Date:  2018-09-21       Impact factor: 10.047

  4 in total

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