Literature DB >> 17252692

Longitudinal study on thyroid function in patients with thalassemia major.

A Filosa1, S Di Maio, G Aloj, C Acampora.   

Abstract

UNLABELLED: Primary hypothyroidism is one of the most frequent complications observed in patients suffering from thalassemia. We investigated thyroid function in a group of patients attending the Pediatric Department of Cardarelli Hospital in order to determine in how many patients thyroid function worsened during a 12 year-period of follow up. PATIENTS AND MEASUREMENTS: Fifty patients with beta-thalassemia major (27 females and 23 males), mean age 25.7+/-1.4 years, were re-evaluated according to the criteria of Faglia et al. Thyroid dysfunction was defined as follows: overt hypothyroidism (low FT4 and increased TSH levels >10 microU/ml); compensated hypothyroidism (normal FT4, TSH 5-10 microU/ml, and abnormal TRH test); subclinical hypothyroidism (normal FT4, basal TSH 0-5 microU/ml, abnormal TRH test). Correlation with hematological, biochemical and growth parameters was evaluated.
RESULTS: Ten out of 50 patients evaluated in a previous study had moved to other centers, and four patients had died from cardiac problems. Thus, 36 patients completed a 12 year-period of follow-up. In 25% of the patients the degree of thyroid dysfunction worsened with different degrees of severity. The prevalence of overt hypothyroidism had risen to 13.9% from 8.4%. No cases of secondary hypothyroidism were observed, and anti-thyroglobulin and anti-thyroperoxidase (TPO) antibody titers were negative in all patients. Five (28%) out of 17 patients with normal thyroid function previously (one female, four male) showed an exaggerated TSH response to a TRH test, with normal serum levels of FT4, and they were classified as having subclinical hypothyroidism; while another patient died of cardiac complications. Four out of twelve patients with previous subclinical hypothyroidism showed worsening with a different degree of severity: two females changed to compensated hypothyroidism, and two males to overt hypothyroidism. Furthermore, two out of six patients with compensated hypothyroidism and one out of four patients with overt hypothyroidism died of cardiac failure. In all patients there was no correlation between serum ferritin levels, blood transfusion, pretransfusion Hb levels and worsening of thyroid function. Echographic data showed features of dishomogeneity of the parenchyma with different degrees of severity in accordance with the criteria of Sostre and Reyes. The highest score was observed in all patients with overt and compensated hypothyroidism.
CONCLUSIONS: A slow worsening of thyroid function was observed in 25% of the studied patients and only two of them developed overt hypothyroidism. The echographic pattern seems to be strongly predictive of thyroid dysfunction.

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Year:  2006        PMID: 17252692     DOI: 10.1515/jpem.2006.19.12.1397

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  8 in total

1.  Evaluation of growth, puberty and endocrine dysfunctions in relation to iron overload in multi transfused Indian thalassemia patients.

Authors:  Rashid H Merchant; Amruta Shirodkar; Javed Ahmed
Journal:  Indian J Pediatr       Date:  2011-01-14       Impact factor: 1.967

Review 2.  Growth and endocrine function in thalassemia major in childhood and adolescence.

Authors:  M Delvecchio; L Cavallo
Journal:  J Endocrinol Invest       Date:  2010-01       Impact factor: 4.256

3.  Prevalence of endocrinopathies in patients with Beta-thalassaemia major - a cross-sectional study in oman.

Authors:  Waad-Allah Mula-Abed; Huda Al Hashmi; Muhanna Al Muslahi; Hilal Al Muslahi; Mohammad Al Lamki
Journal:  Oman Med J       Date:  2008-10

4.  Longitudinal study on thyroid function in patients with thalassemia major: High incidence of central hypothyroidism by 18 years.

Authors:  Ashraf T Soliman; Fawzia Al Yafei; Lolwa Al-Naimi; Noora Almarri; Aml Sabt; Mohamed Yassin; Vincenzo De Sanctis
Journal:  Indian J Endocrinol Metab       Date:  2013-11

Review 5.  Chronic anemia and thyroid function.

Authors:  Ashraf T Soliman; Vincenzo De Sanctis; Mohamed Yassin; Magda Wagdy; Nada Soliman
Journal:  Acta Biomed       Date:  2017-04-28

6.  Health Status of Patients With β-Thalassemia in the West Bank: A Retrospective-Cohort Study.

Authors:  Reem Aldwaik; Tamara Abu Mohor; Israa Idyabi; Salam Warasna; Shatha Abdeen; Bashar Karmi; Rania Abu Seir
Journal:  Front Med (Lausanne)       Date:  2021-12-20

7.  A cross-sectional study of metabolic and endocrine complications in beta-thalassemia major.

Authors:  Farzad Najafipour; Akbar Aliasgarzadeh; Naser Aghamohamadzadeh; Amir Bahrami; Majid Mobasri; Mitra Niafar; Manouchehr Khoshbaten
Journal:  Ann Saudi Med       Date:  2008 Sep-Oct       Impact factor: 1.526

8.  Thyroid Function in Chronically Transfused Children with Beta Thalassemia Major: A Cross-Sectional Hospital Based Study.

Authors:  Suraj Haridas Upadya; M S Rukmini; Sowmya Sundararajan; B Shantharam Baliga; Nutan Kamath
Journal:  Int J Pediatr       Date:  2018-09-16
  8 in total

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