Antonella Meloni, Laura Pistoia, Paolo Ricchi, Filomena Longo, Valerio Cecinati, Francesco Sorrentino, Zelia Borsellino, Elisabetta Corigliano, Vincenza Rossi, Michela Zerbini, Priscilla Fina, Luigi Barbuto, Vincenzo Positano, Alberto Clemente
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引用次数: 0
Abstract
This cross-sectional study compared the prevalence of vascular, hepatic, cardiac, endocrine, and bone complications between adult patients with non-transfusion-dependent thalassemia (NTDT) and neo-transfusion-dependent thalassemia (neo-TDT). We evaluated 97 NTDT patients (44.73 ± 12.98 years, 48.5 % females) and 140 neo-TDT (>4 transfusions/year) patients (44.30 ± 12.13 years, 56.4 % females), enrolled in the Extension-Myocardial Iron Overload in Thalassemia project. Iron overload (IO) was assessed by magnetic resonance imaging and complications were defined by established clinical criteria. Neo-TDT patients had significantly higher hemoglobin and ferritin levels and a higher prevalence of hepatitis C virus infection. Hepatic IO was more common in NTDT patients, whereas pancreatic and cardiac IO were significantly more frequent in the neo-TDT group. No significant differences were observed in extramedullary hematopoiesis, leg ulcers, hepatic cirrhosis, thrombosis, or pulmonary hypertension. Cardiac arrhythmias and impaired glucose metabolism were significantly more prevalent among neo-TDT patients. Hypogonadism, hypothyroidism, and hypoparathyroidism were more frequent in neo-TDT patients, though not statistically significant. Bone disorders were the most common in both groups, with a significantly higher prevalence in neo-TDT. In conclusion, neo-TDT patients exhibited a greater burden of cardiac arrhythmias, glucose metabolism disturbances, and bone metabolism disorders, highlighting the need for comprehensive and early multi-organ monitoring and timely intervention strategies.
期刊介绍:
Blood Cells, Molecules & Diseases emphasizes not only blood cells, but also covers the molecular basis of hematologic disease and studies of the diseases themselves. This is an invaluable resource to all those interested in the study of hematology, cell biology, immunology, and human genetics.