FREQUENCY OF HYPOTHYROIDISM IN PATIENT WITH BETA THALASSEMIA MAJOR
Main Article Content
Keywords
Hypothyroidism, beta thalassemia, pediatric patients, monitoring.
Abstract
Background: Hypothyroidism is a frequently seen result of beta thalassemia. The objective of this research was to assess the prevalence of the phenomenon and examine its associations with patient features and the duration of transfusions.
Objective: the goal of this cross-sectional study at the Thalassemia Centre was to ascertain the frequency of hypothyroidism among 72 pediatric patients with beta thalassemia major, as well as any associations with age, transfusion duration, and serum ferritin.
Study design: A cross-sectional study.
Duration and place of study: The department of pediatrics Combined Military Hospital Rawalpindi from 05-July 2023 to 05-Dec 2023
Methods: There are seventy-two patients with significant beta thalassemia. The mean age of the patients was 11.72 ± 4.03 years. n=72 patients (65.3%), with 34.7 percent of the female and male both patients being 6 to 13-year. Participants in this cross-sectional research gave information on their demographics, serum ferritin, T4, TSH, and duration of transfusion at the Thalassemia Centre. For the analysis, SPSS version 26.0 was used. Of the participants, N-4 (13.8%) had overt hypothyroidism, while N-25 (86.2%) had subclinical hypothyroidism, which accounted for N-62 (86.1%). The patient's age and the length of the transfusion had a significant correlation with the prevalence of hypothyroidism. To sum up, prompt management of hypothyroidism and consistent observation are essential for enhancing the well-being of people with beta thalassemia major.
Results: The research included 72 pediatric patients who were diagnosed with beta thalassemia major. The patients' average age was 11.72 ± 4.03 years, with a significant number of male (65.3%) and female patients (34.7%). Among the male patients, the age range changed into 06 to 12 years, while female patients were between 6 and 13 years old. Of the 72 pediatric patients included in the study, 29 (40.3%) have been diagnosed with hypothyroidism. Among these, 25 patients (86.2%) exhibited subclinical hypothyroidism, characterized by way of regular T4 levels with elevated TSH levels. Only four patients (13.8%) were diagnosed with overt hypothyroidism, offering with low T4 levels in conjunction with higher TSH levels.
Conclusion: The study highlights the significance of regular surveillance and prompt intervention for hypothyroidism in pediatric individuals diagnosed with beta thalassemia major, with a particular focus on its notable correlation with patient age and length of transfusion.
References
2. Ali S, Mumtaz S, Shakir HA, Khan M, Tahir HM, Mumtaz S, Mughal TA, Hassan A, Kazmi SA, Sadia, Irfan M. Current status of beta‐thalassemia and its treatment strategies. Molecular genetics & genomic medicine. 2021 Dec;9(12):e1788.
3. Toumba M, Sergis A, Kanaris C, Skordis N. Endocrine complications in patients with Thalassaemia Major. Pediatric endocrinology reviews. 2007 Dec 1;5(2):642.
4. De Sanctis V, Soliman AT, Elsedfy H, Skordis N, Kattamis C, Angastiniotis M, Karimi M, Yassin MA, El Awwa A, Stoeva I, Raiola G. Growth and endocrine disorders in thalassemia: The international network on endocrine complications in thalassemia (I-CET) position statement and guidelines. Indian journal of endocrinology and metabolism. 2013 Jan 1;17(1):8-18.
5. De Sanctis V, Soliman AT, Canatan D, Yassin MA, Daar S, Elsedfy H, Di Maio S, Raiola G, Corrons JL, Kattamis C. Thyroid disorders in homozygous β-thalassemia: current knowledge, emerging issues and open problems. Mediterranean journal of hematology and infectious diseases. 2019;11(1).
6. Hashemizadeh H, Noori R. Assessment of hypothyroidism in children with beta-thalassemia major in north eastern Iran. Iranian Journal of Pediatric Hematology and Oncology. 2012 Sep 10;2(3):123-7.
7. De Sanctis V, Elsedfy H, Soliman AT, Elhakim IZ, Kattamis C, Soliman NA, Elalaily R. Clinical and biochemical data of adult thalassemia major patients (TM) with multiple endocrine complications (MEC) versus TM patients with normal endocrine functions: A long-term retrospective study (40 years) in a tertiary care center in Italy. Mediterranean Journal of Hematology and Infectious Diseases. 2016;8(1).
8. Macvanin MT, Gluvic Z, Zafirovic S, Gao X, Essack M, Isenovic ER. The protective role of nutritional antioxidants against oxidative stress in thyroid disorders. Frontiers in Endocrinology. 2023 Jan 4;13:1092837.
9. Garber JR, Cobin RH, Gharib H, Hennessey JV, Klein I, Mechanick JI, Pessah-Pollack R, Singer PA, Woeber for the American Association of Clinical Endocrinologists and American Thyroid Association Taskforce on Hypothyroidism in Adults KA. Clinical practice guidelines for hypothyroidism in adults: cosponsored by the American Association of Clinical Endocrinologists and the American Thyroid Association. Thyroid. 2012 Dec 1;22(12):1200-35.
10. Rose SR, Wassner AJ, Wintergerst KA, Yayah-Jones NH, Hopkin RJ, Chuang J, Smith JR, Abell K, LaFranchi SH, SECTION ON ENDOCRINOLOGY EXECUTIVE COMMITTEE Wintergerst Kupper A. MD, FAAP Bethin Kathleen E. MD, FAAP Brodsky Jill L. MD, FAAP Jelley David H. MD, FAAP Marshall Bess A. MD, FAAP Mastrandrea Lucy D. MD, PhD, FAAP Lynch Jane L. MD, FAAP Laskosz Laura MPH. Congenital hypothyroidism: screening and management. Pediatrics. 2023 Jan 1;151(1):e2022060420.
11. De Sanctis V, Soliman AT, Canatan D, Yassin MA, Daar S, Elsedfy H, Di Maio S, Elalaily R, Millimaggi G, Kattamis C. How to screen, evaluate and treat hypothyroidism in homozygous β-thalassemia (β-thal) patients. Rivista Italiana di Medicina dell’Adolescenza-Volume. 2019;17(1).
12. De Sanctis V, Soliman AT, Elsedfy H, Di Maio S, Canatan D, Soliman N, Karimi M, Kattamis C. Gonadal dysfunction in adult male patients with thalassemia major: an update for clinicians caring for thalassemia. Expert review of hematology. 2017 Dec 2;10(12):1095-106.
13. Borgna-Pignatti C, Gamberini MR. Complications of thalassemia major and their treatment. Expert review of hematology. 2011 Jun 1;4(3):353-66.