Risk factors for heart disease in transfusion-dependent thalassemia: serum ferritin revisited

被引:12
|
作者
Derchi, Giorgio [1 ]
Dessi, Carlo [2 ]
Bina, Patrizio [2 ]
Cappellini, Maria Domenica [3 ]
Piga, Antonio [4 ]
Perrotta, Silverio [5 ]
Tartaglione, Immacolata [5 ]
Giuditta, Marianna [3 ]
Longo, Filomena [4 ]
Origa, Raffaella [6 ]
Quarta, Antonella [7 ]
Pinto, Valeria [8 ]
Forni, Gian Luca [8 ]
机构
[1] Osped Galliera, Unita Cardiol, Genoa, Italy
[2] Osped Reg Microcitemie, ASL8, Cagliari, Italy
[3] Univ Milan, Dept Clin Sci & Commun, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Milan, Italy
[4] Univ Torino, Dept Clin & Biol Sci, Turin, Italy
[5] Seconda Univ Napoli, Dipartimento Donna Bambino Chirurg Gen & Speciali, Naples, Italy
[6] Univ Cagliari, Thalassemia Unit, Dept Publ Hlth Clin & Mol Med, Cagliari, Italy
[7] Ematol Osped A Perrino, Brindisi, Italy
[8] Osped Galliera, Ematol Ctr Microcitemia & Anemie Congenite, Via Volta 6, I-16128 Genoa, Italy
关键词
Thalassemia; Heart disease; Iron overload; Serum ferritin; RANDOMIZED CONTROLLED-TRIAL; MAJOR PATIENTS; IRON OVERLOAD; MYOCARDIAL IRON; FOLLOW-UP; DEFEROXAMINE; DEFERASIROX; MANAGEMENT; COMPLICATIONS; DEFERIPRONE;
D O I
10.1007/s11739-018-1890-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Heart disease remains a leading cause of morbidity and mortality in transfusion-dependent thalassemia (TDT), which can be attributed to several factors but primarily develops in the setting of iron overload. This was a retrospective cohort study utilizing Webthal (R) patient data from five major centers across Italy. Patients without heart disease were followed-up for 10 years (2000-2010) and data were collected for demographics, splenectomy status, serum ferritin and hemoglobin levels, and comorbidities associated with heart disease. Among 379 patients analyzed (mean age 22.9 +/- 5.1years, 47.8% men), 44 (cumulative incidence: 11.6%) developed heart disease during the period of observation. Splenectomy (p=0.002) and serum ferritin level (p<0.001) were the only risk factors with significant association with heart disease. A serum ferritin threshold of >= 3000 ng/mL was the best predictor for the development of heart disease (86.4% sensitivity and 92.8% specificity, AUC: 0.912, 95% CI 0.852-0.971, p<0.001). On multivariate analysis, only a serum ferritin level >= 3000 ng/mL remained significantly and independently associated with increased risk of heart disease (HR: 44.85, 95% CI 18.85-106.74), with a 5- and 10-year heart disease-free survival of 58 and 39%. The association between iron overload and heart disease in patients with TDT is confirmed, yet a new serum ferritin level of 3000 ng/mL to flag increased risk is suggested.
引用
收藏
页码:365 / 370
页数:6
相关论文
共 50 条
  • [31] Management of the aging beta-thalassemia transfusion-dependent population - The Italian experience
    Pinto, Valeria Maria
    Poggi, Maurizio
    Russo, Rodolfo
    Giusti, Andrea
    Forni, Gian Luca
    BLOOD REVIEWS, 2019, 38
  • [32] Anthropometric measurements in children having transfusion-dependent beta thalassemia
    Moiz, Bushra
    Habib, Aysha
    Sawani, Sobiya
    Raheem, Ahmed
    Hasan, Bilal
    Gangwani, Manesh
    HEMATOLOGY, 2018, 23 (04) : 248 - 252
  • [33] Safety and efficacy of iron chelation therapy with deferiprone in patients with transfusion-dependent thalassemia
    Jamuar, Saumya S.
    Lai, Angeline H. M.
    THERAPEUTIC ADVANCES IN HEMATOLOGY, 2012, 3 (05) : 299 - 307
  • [34] Magnitude of Bone Disease in Transfusion-Dependent and Non-Transfusion-Dependent β-Thalassemia Patients
    Shamoon, Rawand P.
    Yassin, Ahmed K.
    Omar, Negar
    Saeed, Muhammad D.
    Akram, Reving
    Othman, Naska N.
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (03)
  • [35] Differential effects of iron chelators on iron burden and long-term morbidity and mortality outcomes in a large cohort of transfusion-dependent β-thalassemia patients who remained on the same monotherapy over 10 years
    Musallam, Khaled M.
    Barella, Susanna
    Origa, Raffaella
    Ferrero, Giovanni Battista
    Lisi, Roberto
    Pasanisi, Annamaria
    Longo, Filomena
    Gianesin, Barbara
    Forni, Gian Luca
    BLOOD CELLS MOLECULES AND DISEASES, 2024, 107
  • [36] Magnetic resonance imaging during management of patients with transfusion-dependent thalassemia: a single-center experience
    Karakas, Zeynep
    Yilmaz, Yasin
    Bayramoglu, Zuhal
    Karaman, Serap
    Aydogdu, Selime
    Karagenc, Ayse Ozkan
    Tugcu, Deniz
    Dursun, Memduh
    RADIOLOGIA MEDICA, 2018, 123 (08): : 572 - 576
  • [37] Study of platelet activation, hypercoagulable state, and pulmonary hypertension in patients with transfusion-dependent beta-thalassemia
    Haji, Lanja Othman
    Polus, Ranan Kardagh
    Mohammed, Nawsherwan Sadiq
    IRAQI JOURNAL OF HEMATOLOGY, 2024, 13 (02) : 334 - 339
  • [38] Relationship between serum ferritin and growth status of pediatric transfusion dependent thalassemia
    Cahyadi, Andi
    Ugrasena, I. Dewa Gede
    Andarsini, Mia Ratwita
    Larasati, Maria Christina Shanty
    Jauhari, Raden Muhammad Zulfan
    Arumsari, Diah Kusuma
    CASPIAN JOURNAL OF INTERNAL MEDICINE, 2023, 14 (03) : 425 - 432
  • [39] Endocrinopathies in patients with transfusion-dependent ß-thalassemia
    Mehrvar, A.
    Azarkeivan, A.
    Faranoush, M.
    Mehrvar, N.
    Saberinedjad, J.
    Ghorbani, R.
    Vossough, P.
    PEDIATRIC HEMATOLOGY AND ONCOLOGY, 2008, 25 (03) : 187 - 194
  • [40] Effect of different iron chelation regimens on bone mass in transfusion-dependent thalassemia patients
    Bordbar, Mohammadreza
    Haghpanah, Sezaneh
    Zekavat, Omid Reza
    Saki, Forough
    Bazrafshan, Asghar
    Bozorgi, Haleh
    EXPERT REVIEW OF HEMATOLOGY, 2019, 12 (11) : 997 - 1003