National networking in rare diseases and reduction of cardiac burden in thalassemia major

Author:

Pepe Alessia1,Pistoia Laura1ORCID,Gamberini Maria Rita2,Cuccia Liana3,Lisi Roberto4,Cecinati Valerio5,Maggio Aurelio6,Sorrentino Francesco7,Filosa Aldo8ORCID,Rosso Rosamaria9,Messina Giuseppe10,Missere Massimiliano11,Righi Riccardo12ORCID,Renne Stefania13,Vallone Antonino14,Dalmiani Stefano15ORCID,Positano Vincenzo1ORCID,Midiri Massimo16,Meloni Antonella1ORCID

Affiliation:

1. Magnetic Resonance Imaging Unit, Fondazione G. Monasterio CNR-Regione Toscana, Via Moruzzi 1, Pisa 56124, Italy

2. Dipartimento della Riproduzione e dell’Accrescimento, Day Hospital della Talassemia e delle Emoglobinopatie, Azienda Ospedaliero-Universitaria Arcispedale “S. Anna”, Via Aldo Moro 8, Ferrara 44124, Italy

3. Unità Operativa Complessa Ematologia con Talassemia, ARNAS Civico “Benfratelli-Di Cristina”, Piazza N. Leotta 4, Palermo 90134, Italy

4. Unità Operativa Dipartimentale Talassemia, Presidio Ospedaliero Garibaldi-Centro—ARNAS Garibaldi, Piazza Santa Maria di Gesù 7, Catania 95100, Italy

5. Struttura Semplice di Microcitemia, Ospedale “SS. Annunziata” ASL Taranto, Via Bruno 1, Taranto 74123, Italy

6. Ematologia II con Talassemia, Ospedale “V. Cervello”, Via Trabucco 180, Palermo 90100, Italy

7. Unità Operativa Semplice Dipartimentale Day Hospital Talassemici, Ospedale “Sant'Eugenio”, Piazzale Umanesimo 10, Roma 00143, Italy

8. Unità Operativa Semplice Dipartimentale Malattie Rare del Globulo Rosso, Azienda Ospedaliera di Rilievo Nazionale “A. Cardarelli”, Via Cardarelli 9, Napoli 80131, Italy

9. Unità Operativa Talassemie ed Emoglobinopatie, Azienda Ospedaliero-Universitaria Policlinico “Vittorio Emanuele”, Via S. Sofia 74, Catania 95100, Italy

10. Centro Microcitemie, Azienda Ospedaliera “Bianchi-Melacrino-Morelli”, Viale Europa, Reggio Calabria 89100, Italy

11. Dipartimento di Immagini, Fondazione di Ricerca e Cura “Giovanni Paolo II”, Largo A. Gemelli 1, Campobasso 86100, Italy

12. Diagnostica per Immagini e Radiologia Interventistica, Ospedale del Delta, Via Valle Oppio 2, Lagosanto, FE 44023, Italy

13. Struttura Complessa di Cardioradiologia-UTIC, Presidio Ospedaliero “Giovanni Paolo II”, Via A. Perugini, Lamezia Terme, CZ 88046, Italy

14. Reparto di Radiologia, Azienda Ospedaliera “Garibaldi” Presidio Ospedaliero Nesima, Via Palermo 636, Catania 95126, Italy

15. Unità Operativa Sistemi Informatici, Fondazione G. Monasterio CNR-Regione Toscana, Via Moruzzi 1, Pisa 56124, Italy

16. Sezione di Scienze Radiologiche—Dipartimento di Biopatologia e Biotecnologie Mediche, Policlinico “Paolo Giaccone”, Via del Vespro 127, Palermo 90127, Italy

Abstract

Abstract Aims A tailored chelation therapy guided by magnetic resonance imaging (MRI) is a strategy to improve the prognosis in iron-loaded patients, in many cases still hampered by limited MRI availability. In order to address this issue, the Myocardial Iron Overload in Thalassemia (MIOT) network was established in Italy and we aimed to describe the impact of 10-year activity of this network on cardiac burden in thalassemia major (TM). Methods and results Within the MIOT network, 1746 TM patients (911 females; mean age 31.2 ± 9.1 years) were consecutively enrolled and prospectively followed by 70 thalassemia and 10 MRI centres. Patients were scanned using a multiparametric approach for assessing myocardial iron overload (MIO), biventricular function, and myocardial fibrosis. At the last MRI scan, a significant increase in global heart T2* values and a significantly higher frequency of patients with no MIO (all segmental T2* ≥20 ms) were detected, with a concordant improvement in biventricular function, particularly in patients with baseline global heart T2* <20 ms. Forty-seven percentage of patients changed the chelation regimen based on MRI. The frequency of heart failure (HF) significantly decreased after baseline MRI from 3.5 to 0.8% (P < 0.0001). Forty-six patients died during the study, and HF accounted for 34.8% of deaths. Conclusion Over 10 years, continuous monitoring of cardiac iron and a tailored chelation therapy allowed MIO reduction, with consequent improvement of cardiac function and reduction of cardiac complications and mortality from MIO-related HF. A national networking for rare diseases therefore proved effective in improving the care and reducing cardiac outcomes of TM patients. Key Question Which was the impact on cardiac outcomes in thalassemia major by a national network among thalassemia and magnetic resonance imaging centres ensuring the continuous and standardized monitoring of the cardiac iron levels? Key Finding There was a reduction of myocardial iron overload (MIO) in almost 70% of patients, with consequent improvement of cardiac function and reduction of cardiac complications and mortality from MIO-related heart failure. Take Home Message A national clinical and imaging networking in rare diseases was effective in improving the care and in reducing the cardiac burden in thalassemia major patients.

Funder

Chiesi Farmaceutici S.p.A. and ApoPharma Inc.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Reference45 articles.

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