Literature DB >> 24854890

Endocrinopathies in Turkish children with Beta thalassemia major: results from a single center study.

Pamir Isik1, Nese Yarali, Betül Tavil, Fatma Demirel, Gülşah Bayram Karacam, Rukiye Unsal Sac, Ali Fettah, Serdar Ozkasap, Abdurrahman Kara, Bahattin Tunc.   

Abstract

The endocrinological complications in β-thalassemia major patients do affect the life quality to a large extend. In this study, the endocrinological complications of 47 β-thalassemia patients, who have been followed-up at our hospital's pediatric hematology department, were evaluated. Out of β-thalassemia major cases included to this study, the 55.3% was male and 44.7% was female. The patients' mean levels of ferritin, whose mean age was 10.0 ± 4.5 years (2-20 years), were 2497 ± 1469 ng/mL (472-8558 ng/mL). At least one endocrinological pathology in 27 out of 47 (57.4%) and more than one endocrinological pathology in 14 out of 47 (29.7%) thalassemia patients were observed. The most frequently observed complication in followed-up cases was vitamin D insufficiency and deficiency (78.2%). The other complications in decreasing order were pubertal failure (41.6%), growth retardation (25.5%), decreased bone-mineral density (22.2%), secondary hyperparathyroidism (11.5%), overt hypothyroidism (4.25%), subclinical hypothyroidism (2.12%), and impaired glucose tolerance (2.12%). There was no statistically significant difference between serum mean ferritin level and endocrin complications (P > .05). Four patients (8.5%) had decreased signal intensity in pituitary magnetic resonance imaging (MRI) but this finding was not associated with ferritin levels (P = .87). MRI parameters were similar between patients with and without gonadal dysfunction. Mean height of the pituitary gland was 4.98 ± 1.1 mm (3-9 mm) and this was similar to those normal values in the literature. Ferritin levels were not correlated with pituitary height (P > .05). Beta thalassemia major, having the potential of leading to multisystemic complications, is a chronic disease that should be treated and followed-up by a multidisciplinary approach. Due to frequently encountered endocrinological complications, beta thalassemic patients should be followed-up regularly by hematology and endocrinology departments in coordination.

Entities:  

Keywords:  endocrinology; pediatrics; radiology; thalassemia

Mesh:

Substances:

Year:  2014        PMID: 24854890     DOI: 10.3109/08880018.2014.898724

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN: 0888-0018            Impact factor:   1.969


  12 in total

1.  Prevalence of endocrine disorders and their associated factors in transfusion-dependent thalassemia patients: a historical cohort study in Southern Iran.

Authors:  M Bordbar; H Bozorgi; F Saki; S Haghpanah; M Karimi; A Bazrafshan; O R Zekavat
Journal:  J Endocrinol Invest       Date:  2019-06-21       Impact factor: 4.256

2.  Prevalence of growth and endocrine disorders in Malaysian children with transfusion-dependent thalassaemia.

Authors:  Khian Aun Tan; Su Han Lum; Abqariyah Yahya; Shekhar Krishnan; Muhammad Yazid Jalaludin; Way Seah Lee
Journal:  Singapore Med J       Date:  2018-12-17       Impact factor: 1.858

3.  Nutrition in Thalassemia: A Systematic Review of Deficiency, Relations to Morbidity, and Supplementation Recommendations.

Authors:  Elijah K Goldberg; Ashutosh Lal; Ellen B Fung
Journal:  J Pediatr Hematol Oncol       Date:  2022-01-01       Impact factor: 1.289

4.  Association of VDBP rs4701 Variant, but not VDR/RXR-α Over-Expression with Bone Mineral Density in Pediatric Well-Chelated β-Thalassemia Patients.

Authors:  Shaimaa Sahmoud; Mostafa S Ibrahim; Eman A Toraih; Noha Kamel; Manal S Fawzy; Samar Elfiky
Journal:  Mediterr J Hematol Infect Dis       Date:  2020-07-01       Impact factor: 2.576

Review 5.  Vitamin D and bone health status in beta thalassemia patients-systematic review.

Authors:  P P Manolopoulos; G Lavranos; I Mamais; A Angouridis; K Giannakou; E O Johnson
Journal:  Osteoporos Int       Date:  2021-01-09       Impact factor: 4.507

Review 6.  Prevalence of diabetes, impaired fasting glucose and impaired glucose tolerance in patients with thalassemia major in Iran: A meta-analysis study.

Authors:  Milad Azami; Ali Sharifi; Siros Norozi; Akram Mansouri; Kourosh Sayehmiri
Journal:  Caspian J Intern Med       Date:  2017

7.  Complications and Challenges in the Management of Iraqi Patients with β-Thalassemia Major: A Single-center Experience.

Authors:  Regir K Sadullah; Sulav D Atroshi; Nasir A Al-Allawi
Journal:  Oman Med J       Date:  2020-07-27

8.  Moderate to severe liver siderosis and raised AST are independent risk factors for vitamin D insufficiency in β-thalassemia patients.

Authors:  Hadi Darvishi-Khezri; Hossein Karami; Mohammad Naderisorki; Mohammad Zahedi; Alireza Razavi; Mehrnoush Kosaryan; Aily Aliasgharian
Journal:  Sci Rep       Date:  2020-12-03       Impact factor: 4.379

9.  Investigating the Role of Ferritin in Determining Sexual Underdevelopment in Beta-Thalassemia Major Patients: A Cross-Sectional Analysis From Pakistan.

Authors:  Zia Shahid; Sarmad Hassan; Saqlain Ghazanfar; Mehwish Kaneez; Muhammad Sheharyar Khan; Hafiz Tanveer Tariq; Arslan Jawad; Atifa Shuaib; Assadullah Akram Bhatti; Mustafa Tauseef Razzaq
Journal:  Cureus       Date:  2021-06-10

10.  Complications of Transfusion-Dependent β-Thalassemia Patients in Sistan and Baluchistan, South-East of Iran.

Authors:  Maryam Yaghobi; Ebrahim Miri-Moghaddam; Naderi Majid; Ali Bazi; Ali Navidian; Asiyeh Kalkali
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2017-10-01
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