GH/IGF-1 axis in a large cohort of ß-thalassemia major adult patients: a cross-sectional study

Author:

Gagliardi I.ORCID,Mungari R.,Gamberini M. R.,Fortini M.,Dassie F.ORCID,Putti M. C.,Maffei P.,Aliberti L.ORCID,Bondanelli M.ORCID,Zatelli M. C.ORCID,Ambrosio M. R.ORCID

Abstract

Abstract Purpose GH deficit (GHD) could represent an endocrine issue in ß-Thalassemia Major (ßTM) patients. GH/IGF-1 axis has not been extensively explored in ßTM adults, so far. We aim to assess GHD and IGF-1 deficiency prevalence in ßTM adult population, focusing on the relationship with liver disease. Methods Cross-sectional multi-centre study conducted on 81 adult ßTM patients (44 males, mean age 41 ± 8 years) on transfusion and chelation therapy. GHD was investigated by GHRH + arginine test. IGF-1 levels, routine biochemical exams, Fibroscan, Hepatic Magnetic Resonance Imaging (MRI) and pituitary MRI were collected. Results Eighteen patients were affected by GHD and 63 were not (nGHD) according to GHRH + arginine test, while basal GH levels did not differ. GHD was associated with a higher BMI and a worse lipid profile (p < 0.05). No significant differences were observed regarding liver function between the two groups. Pituitary MRI scan was normal except for one case of empty sella. The 94.4% and 93.6% of GHD and nGHD, respectively, presented lower IGF-1 levels than the reference range, and mean IGF-1 SDS was significantly lower in GHD patients. Conclusion GHD is frequent in adult ßTM patients and is associated with higher BMI and worse lipid profile. nGHD patients present lower IGF-1 levels as well. There was no relationship between IGF-1 levels and liver disease. Further, multicentric studies with larger cohorts and standardized diagnostic protocols are needed.

Funder

FAR 2018

FAR 2019

FAR 2020

Open access funding provided by Università degli Studi di Ferrara within the CRUI-CARE Agreement.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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3. Approach to the Patient: A Case With an Unusual Cause of Hypopituitarism;The Journal of Clinical Endocrinology & Metabolism;2022-12-27

4. New Entity—Thalassemic Endocrine Disease: Major Beta-Thalassemia and Endocrine Involvement;Diagnostics;2022-08-09

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