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Statural growth and prevalence of endocrinopathies in relation to liver iron content (LIC) in adult patients with beta thalassemia major (BTM) and sickle cell disease (SCD)

Despite regular blood transfusion and iron chelation therapy, growth impairment and pubertal delay are commonly seen in children and adolescents with transfusion-dependent Beta thalassaemia major (BTM) and sickle cell disease (SCD). We evaluated growth parameters and endocrine disorders in relation...

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Autores principales: Yassin, Mohamed A, Soliman, Ashraf T, de Sanctis, Vincenzo, Abdula, Mohammad AJ, Riaz, Lubna M, Ghori, Firdous F, Yousaf, Anil, Nashwan, Abdulqadir J, Abusamaan, Sandara, Moustafa, Abbas, Kohla, Samah, Soliman, Dina S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179035/
https://www.ncbi.nlm.nih.gov/pubmed/29451227
http://dx.doi.org/10.23750/abm.v89i2-S.7085
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author Yassin, Mohamed A
Soliman, Ashraf T
de Sanctis, Vincenzo
Abdula, Mohammad AJ
Riaz, Lubna M
Ghori, Firdous F
Yousaf, Anil
Nashwan, Abdulqadir J
Abusamaan, Sandara
Moustafa, Abbas
Kohla, Samah
Soliman, Dina S
author_facet Yassin, Mohamed A
Soliman, Ashraf T
de Sanctis, Vincenzo
Abdula, Mohammad AJ
Riaz, Lubna M
Ghori, Firdous F
Yousaf, Anil
Nashwan, Abdulqadir J
Abusamaan, Sandara
Moustafa, Abbas
Kohla, Samah
Soliman, Dina S
author_sort Yassin, Mohamed A
collection PubMed
description Despite regular blood transfusion and iron chelation therapy, growth impairment and pubertal delay are commonly seen in children and adolescents with transfusion-dependent Beta thalassaemia major (BTM) and sickle cell disease (SCD). We evaluated growth parameters and endocrine disorders in relation to the liver iron concentration (LIC) assessed by the Ferriscan® method in a cohort of adults with SCD (n=40) and BTM (n=52) receiving blood transfusions and iron chelation therapy since early childhood. Before transfusion, hemoglobin concentration had not been less than 9 g/dl in the past 12 years; subcutaneous daily desferrioxamine was administered for all of them since early childhood (2-5 years of age). All patients were shifted to oral therapy with deferasirox iron chelation, 20 mg/daily for the past 5 years. BTM patients with higher LIC (>15 mg Fe/g dry weight) had significantly shorter stature, lower insulin-like growth factor-I SDS (IGF-I SDS), higher alanine transferase (ALT) and serum ferritin concentrations compared to thalassemic patients with lower LIC. Patients with SCD with LIC >8 mg Fe/g dry weight had significantly shorter stature, lower IGF-I SDS and higher ALT compared to SCD patients with lower LIC. Patients with BTM had significantly shorted final height (Ht-SDS), IGF-I SDS and FT4 level compared to patients with SCD. LIC and mean fasting blood glucose (FBG) were significantly higher in patients with BTM compared to those with SCD. The linear regression analysis showed a significant correlation between LIC and serum ferritin level in SCD and BTM. LIC and serum ferritin level were also correlated significantly with IGF-I level in patients with BTM. LIC was correlated significantly with ALT in patients with BTM. In conclusion, the prevalence of endocrinopathies especially hypothyroidism, DM, and hypogonadism were significantly higher in BTM patients versus SCD patients and higher in patients with higher LIC versus those with lower LIC. These complications occurred less frequently, but still considerable, in chronically transfused patients with SCD. (www.actabiomedica.it)
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spelling pubmed-61790352019-05-08 Statural growth and prevalence of endocrinopathies in relation to liver iron content (LIC) in adult patients with beta thalassemia major (BTM) and sickle cell disease (SCD) Yassin, Mohamed A Soliman, Ashraf T de Sanctis, Vincenzo Abdula, Mohammad AJ Riaz, Lubna M Ghori, Firdous F Yousaf, Anil Nashwan, Abdulqadir J Abusamaan, Sandara Moustafa, Abbas Kohla, Samah Soliman, Dina S Acta Biomed Original Article Despite regular blood transfusion and iron chelation therapy, growth impairment and pubertal delay are commonly seen in children and adolescents with transfusion-dependent Beta thalassaemia major (BTM) and sickle cell disease (SCD). We evaluated growth parameters and endocrine disorders in relation to the liver iron concentration (LIC) assessed by the Ferriscan® method in a cohort of adults with SCD (n=40) and BTM (n=52) receiving blood transfusions and iron chelation therapy since early childhood. Before transfusion, hemoglobin concentration had not been less than 9 g/dl in the past 12 years; subcutaneous daily desferrioxamine was administered for all of them since early childhood (2-5 years of age). All patients were shifted to oral therapy with deferasirox iron chelation, 20 mg/daily for the past 5 years. BTM patients with higher LIC (>15 mg Fe/g dry weight) had significantly shorter stature, lower insulin-like growth factor-I SDS (IGF-I SDS), higher alanine transferase (ALT) and serum ferritin concentrations compared to thalassemic patients with lower LIC. Patients with SCD with LIC >8 mg Fe/g dry weight had significantly shorter stature, lower IGF-I SDS and higher ALT compared to SCD patients with lower LIC. Patients with BTM had significantly shorted final height (Ht-SDS), IGF-I SDS and FT4 level compared to patients with SCD. LIC and mean fasting blood glucose (FBG) were significantly higher in patients with BTM compared to those with SCD. The linear regression analysis showed a significant correlation between LIC and serum ferritin level in SCD and BTM. LIC and serum ferritin level were also correlated significantly with IGF-I level in patients with BTM. LIC was correlated significantly with ALT in patients with BTM. In conclusion, the prevalence of endocrinopathies especially hypothyroidism, DM, and hypogonadism were significantly higher in BTM patients versus SCD patients and higher in patients with higher LIC versus those with lower LIC. These complications occurred less frequently, but still considerable, in chronically transfused patients with SCD. (www.actabiomedica.it) Mattioli 1885 2018 /pmc/articles/PMC6179035/ /pubmed/29451227 http://dx.doi.org/10.23750/abm.v89i2-S.7085 Text en Copyright: © 2018 ACTA BIO MEDICA SOCIETY OF MEDICINE AND NATURAL SCIENCES OF PARMA http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Original Article
Yassin, Mohamed A
Soliman, Ashraf T
de Sanctis, Vincenzo
Abdula, Mohammad AJ
Riaz, Lubna M
Ghori, Firdous F
Yousaf, Anil
Nashwan, Abdulqadir J
Abusamaan, Sandara
Moustafa, Abbas
Kohla, Samah
Soliman, Dina S
Statural growth and prevalence of endocrinopathies in relation to liver iron content (LIC) in adult patients with beta thalassemia major (BTM) and sickle cell disease (SCD)
title Statural growth and prevalence of endocrinopathies in relation to liver iron content (LIC) in adult patients with beta thalassemia major (BTM) and sickle cell disease (SCD)
title_full Statural growth and prevalence of endocrinopathies in relation to liver iron content (LIC) in adult patients with beta thalassemia major (BTM) and sickle cell disease (SCD)
title_fullStr Statural growth and prevalence of endocrinopathies in relation to liver iron content (LIC) in adult patients with beta thalassemia major (BTM) and sickle cell disease (SCD)
title_full_unstemmed Statural growth and prevalence of endocrinopathies in relation to liver iron content (LIC) in adult patients with beta thalassemia major (BTM) and sickle cell disease (SCD)
title_short Statural growth and prevalence of endocrinopathies in relation to liver iron content (LIC) in adult patients with beta thalassemia major (BTM) and sickle cell disease (SCD)
title_sort statural growth and prevalence of endocrinopathies in relation to liver iron content (lic) in adult patients with beta thalassemia major (btm) and sickle cell disease (scd)
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179035/
https://www.ncbi.nlm.nih.gov/pubmed/29451227
http://dx.doi.org/10.23750/abm.v89i2-S.7085
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