Introduction β-thalassemia is an inherited hemoglobinopathy which, in severe cases, requires lifelong transfusions, leading to iron overload and increases risk of metabolic complications, including diabetes mellitus. The standard glycemic marker, glycated hemoglobin, is unreliable in transfusion-dependent patients due to altered erythrocyte turnover. This study investigates the possible utility of glycated albumin as an alternative biomarker for diagnosing glucose metabolism disorders in transfusion-dependent patients. Methods A cross-sectional analysis was conducted on 254 transfusion-dependent patients followed at the Center for Hemoglobinopathies and Thalassemia at Ferrara Hospital, evaluating Glycated Albumin levels, fasting plasma glucose, oral glucose tolerance test results, and iron overload assessed by Magnetic Resonance Imaging. Results Glycated Albumin levels significantly correlated with Fasting Plasma Glucose (r = 0.710, p < 0.01), Oral Glucose Tolerance Test glucose levels at 60 and 120 min, and the area under the glycemic curve (p < 0.01). ROC curve analysis identified a Glycated Albumin cutoff of 14.95% for Diabetes Mellitus diagnosis, with a sensitivity of 93.1% and specificity of 89.1%. Glycated Albumin correlated with hepatic and heart iron accumulation but not with pancreatic iron overload. Conclusions These findings indicate Glycated Albumin as a promising marker for glycemic assessment in transfusion-dependent patients, warranting further validation in multicenter studies.

Glycated albumin as a diagnostic tool for diabetes mellitus in transfusion-dependent β-thalassemia patients

Gianluca Marzi
Writing – Original Draft Preparation
;
Martina Verrienti
Writing – Original Draft Preparation
;
Filomena Longo
Resources
;
Camilla Alice Cattaneo
Data Curation
;
Alberto Gobbo
Data Curation
;
Katalin Vetralla
Investigation
;
Alberto Cossu
Resources
;
Martina Culcasi
Investigation
;
Maria Chiara Zatelli
Formal Analysis
;
Maria Rosaria Ambrosio
Conceptualization
2025

Abstract

Introduction β-thalassemia is an inherited hemoglobinopathy which, in severe cases, requires lifelong transfusions, leading to iron overload and increases risk of metabolic complications, including diabetes mellitus. The standard glycemic marker, glycated hemoglobin, is unreliable in transfusion-dependent patients due to altered erythrocyte turnover. This study investigates the possible utility of glycated albumin as an alternative biomarker for diagnosing glucose metabolism disorders in transfusion-dependent patients. Methods A cross-sectional analysis was conducted on 254 transfusion-dependent patients followed at the Center for Hemoglobinopathies and Thalassemia at Ferrara Hospital, evaluating Glycated Albumin levels, fasting plasma glucose, oral glucose tolerance test results, and iron overload assessed by Magnetic Resonance Imaging. Results Glycated Albumin levels significantly correlated with Fasting Plasma Glucose (r = 0.710, p < 0.01), Oral Glucose Tolerance Test glucose levels at 60 and 120 min, and the area under the glycemic curve (p < 0.01). ROC curve analysis identified a Glycated Albumin cutoff of 14.95% for Diabetes Mellitus diagnosis, with a sensitivity of 93.1% and specificity of 89.1%. Glycated Albumin correlated with hepatic and heart iron accumulation but not with pancreatic iron overload. Conclusions These findings indicate Glycated Albumin as a promising marker for glycemic assessment in transfusion-dependent patients, warranting further validation in multicenter studies.
2025
Marzi, Gianluca; Verrienti, Martina; Longo, Filomena; Cattaneo, Camilla Alice; Gobbo, Alberto; Vetralla, Katalin; Pietro Franzè, Gian; Cossu, Alberto;...espandi
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in SFERA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/2608011
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 0
  • ???jsp.display-item.citation.isi??? 0
social impact