Pancreatic Volume in Thalassemia: Determinants and Association with Alterations of Glucose Metabolism.

Bibliographic Details
Title: Pancreatic Volume in Thalassemia: Determinants and Association with Alterations of Glucose Metabolism.
Authors: Meloni, Antonella, Restaino, Gennaro, Positano, Vincenzo, Pistoia, Laura, Keilberg, Petra, Santodirocco, Michele, Spasiano, Anna, Casini, Tommaso, Serra, Marilena, De Marco, Emanuela, Roberti, Maria Grazia, Bagnato, Sergio, Pepe, Alessia, Clemente, Alberto, Missere, Massimiliano
Source: Diagnostics (2075-4418); Mar2025, Vol. 15 Issue 5, p568, 17p
Subject Terms: MAGNETIC resonance imaging, IRON overload, GLUCOSE metabolism, BODY surface area, IRON metabolism
Abstract: Objectives: This study aimed to compare the pancreatic volume between beta-thalassemia major (β-TM) and beta-thalassemia intermedia (β-TI) patients and between thalassemia patients and healthy subjects and to determine the predictors of pancreatic volume and its association with glucose metabolism in β-TM and β-TI patients. Methods: We considered 145 β-TM patients and 19 β-TI patients enrolled in the E-MIOT project and 20 healthy subjects. The pancreatic volume and pancreatic and hepatic iron levels were quantified by magnetic resonance imaging. Results: The pancreatic volume indexed by body surface area (PVI) was significantly lower in both β-TI and β-TM patients compared to healthy subjects and in β-TM patients compared to β-TI patients. The only independent determinants of PVI were pancreatic iron in β-TM and hepatic iron in β-TI. In β-TM, there was an association between alterations of glucose metabolism and PVI, and PVI was a comparable predictor of altered glucose metabolism compared to pancreatic iron. Only one β-TI patient had an altered glucose metabolism and showed a reduced PVI and pancreatic iron overload. Conclusions: Thalassemia syndromes are characterized by a reduced pancreatic volume, associated with iron levels. In β-TM, the pancreatic volume and iron deposition are associated with the development and progression of alterations of glucose metabolism. [ABSTRACT FROM AUTHOR]
Copyright of Diagnostics (2075-4418) is the property of MDPI and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Complementary Index
Full text is not displayed to guests.
More Details
ISSN:20754418
DOI:10.3390/diagnostics15050568
Published in:Diagnostics (2075-4418)
Language:English