THYROID FUNCTION TEST IN SICKLE-CELL DISEASE

Authors

  • JINGYASA SWAIN Department of General Medicine, MKCG Medical College and Hospital, Berhampur, Odisha, India
  • BISWAJIT MOHANTY Department of General Medicine, Medical College-IMS and SUM Hospital, Bhubaneswar, Odisha, India
  • Nayan kumar patel Department of Cardiology, Medical College, VIMSAR, Sambalpur, Odisha, India
  • chakradhar majhi Department of General Medicine, Medical College-VIMSAR, Sambalpur, Odisha, India

DOI:

https://doi.org/10.22159/ajpcr.2023.v16i7.47607

Keywords:

Sickle-cell anemia, Sickle-cell disease, Hypothyroidism, Thyroid Function test

Abstract

Objective: This cross-sectional study aimed to evaluate the thyroid function (triiodothyronine [T3], thyroxine [T4], and thyroid-stimulating hormone [TSH] levels) in patients with sickle-cell disease (SCD).

Methods: This cross-sectional observational study was conducted in the general medicine department of the Veer Surendra Sai Medical College and Hospital, Burla, Sambalpur, Odisha (India). The investigation was performed in the sickle cell clinic, medical ward, and outpatient department of the institute. This study was conducted from November 2019 to October 2021. Sixty-eight patients with SCD were enrolled for assessing their thyroid function. The reference ranges for serum T4 (4.5–12 μg/dL), serum T3 (60–200 ng/dL), and TSH (0.3–5.5 uIU/mL) were defined to evaluate the thyroid function.

Results: The average TSH, mean T4 level, and mean T3 level among the patients were 4.02, 4.67, and 74.15, respectively. The incidence rates of hypothyroidism and euthyroid status were 23.5% and 76.5%, respectively. While 9.59 g/dL was the mean hemoglobin level, 11–16 g/dL was observed in 42.6% of patients compared to <11 g/dL in 57.4% of patients. Patients within the age group of 14-25 years had a higher incidence of hypothyroidism (62.5%). The differences in hypothyroidism between males and females were statistically insignificant (68.8% vs. 31.2%, p = 0.11).

Conclusion: Patients with SCD had clinically significant reductions in T3 and T4 levels. In addition, higher levels of TSH and reductions in endogenous T3/T4 levels were observed in male patients. Overall, SCD was associated with a higher incidence of hypothyroidism.

Downloads

Download data is not yet available.

Author Biography

Nayan kumar patel, Department of Cardiology, Medical College, VIMSAR, Sambalpur, Odisha, India

Assistant professor, Department of Cardiology, Medical College, VIMSAR, Burla, Sambalpur, Odisha

References

Kohne E. Hemoglobinopathies: Clinical manifestations, diagnosis, and treatment. Dtsch Ärztebl Int 2011;108:532-40.

Savitt TL, Goldberg MF. Herrick’s 1910 case report of sickle cell anemia. The rest of the story. JAMA 1989;261:266-71.

Mason VR. Landmark article Oct. 14, 1922: Sickle cell anemia. By V.R. Mason. JAMA 1985;254:1955-7.

Ilesanmi OO. Pathological basis of symptoms and crises in sickle cell disorder: Implications for counseling and psychotherapy. Hematol Rep 2010;2:e2.

Lubeck D, Agodoa I, Bhakta N, Danese M, Pappu K, Howard R, et al. Estimated life expectancy and income of patients with sickle cell disease compared with those without sickle cell disease. JAMA Network Open 2019;2:e1915374.

Adekile A. The genetic and clinical significance of fetal hemoglobin expression in sickle cell disease. Med Princ Pract 2021;30:201-11.

Williams TN. Sickle cell disease in sub-Saharan Africa. Hematol Oncol Clin North Am 2016;30:343-58.

Raman V, Seshadri T, Joice SV, Srinivas PN. Sickle cell disease in India: a scoping review from a health systems perspective to identify an agenda for research and action. BMJ Global Health 2021;6:e004322.

Wastnedge E, Waters D, Patel S, Morrison K, Goh MY, Adeloye D, et al. The global burden of sickle cell disease in children under five years of age: A systematic review and meta-analysis. J Glob Health 2018;8:021103.

Egesa WI, Nakalema G, Waibi WM, Turyasiima M, Amuje E, Kiconco G, et al. Sickle cell disease in children and adolescents: A review of the historical, clinical, and public health perspective of sub-Saharan Africa and beyond. Int J Pediatr 2022;2022:3885979.

Ceglie G, Di Mauro M, De Jacobis IT, de Gennaro F, Quaranta M, Baronci C, et al. Gender-related differences in sickle cell disease in a pediatric cohort: A single-center retrospective study. Front Mol Biosci 2019;6:140.

Hardison RC. Evolution of hemoglobin and its genes. Cold Spring Harb Perspect Med 2012;2:a011627.

Villegas A, González FA, Nieto JM, de la Fuente-Gonzalo F, Martínez R, Torrejón MJ, et al. Haemoglobinopathies that occur with decreased HbA2levels: A gene mutation set involving the δ gene at a Spanish centre. J Clin Pathol 2017;70:75-80.

Ochocinski D, Dalal M, Black LV, Carr S, Lew J, Sullivan K, et al. Life-threatening infectious complications in sickle cell disease: A concise narrative review. Front Pediatr 2020;8:38.

Sysol JR, Machado R. Sickle cell disease and acute chest syndrome: Epidemiology, diagnosis, management, outcomes. In: Hematologic Abnormalities and Acute Lung Syndromes. Respiratory Medicine. Cham: Humana Press; 2017. p. 67-87.

Shah R, Taborda C, Chawla S. Acute and chronic hepatobiliary manifestations of sickle cell disease: A review. World J Gastrointest Pathophysiol 2017;8:108-16.

Khan A, Nashed B, Issa M, Khan MZ. Sickle cell intrahepatic cholestasis: Extremely rare but fatal complication of sickle cell disease. Cureus 2022;14:e22050.

Ogu UO, Badamosi NU, Camacho PE, Freire AX, Adams-Graves P. Management of sickle cell disease complications beyond acute chest syndrome. J Blood Med 2021;12:101-14.

Yamakawa H, Kato TS, Noh JY, Yuasa S, Kawamura A, Fukuda K, et al. Thyroid hormone plays an important role in cardiac function: From bench to bedside. Front Physiol 2021;12:606931.

Shokripour M, Imanieh MH, Garayemi S, Omidifar N, Yeganeh BS, Althabhawee F. Thyroid stimulating hormone, T3 and T4 population-based reference range and children prevalence of thyroid dysfunction: First report from South of Iran. Iran J Pathol 2022;17:427-34.

Soliman AT, De Sanctis V, Yassin M, Wagdy M, Soliman N. Chronic anemia and thyroid function. Acta Biomed 2017;88:119-27.

Poggiali E, Cassinerio E, Zanaboni L, Cappellini MD. An update on iron chelation therapy. Blood Transfus 2012;10:411-22.

ElAlfy MS, El-Sherif NH, Sakr HM, El Ashkar MN. Thyroid hemodynamic alterations in Egyptian patients with sickle cell disease: Relation to disease severity, total body iron and thyroid function. Expert Rev Hematol 2019;12:589-96.

Özen S, Ünal S, Erçetin N, Taşdelen B. Frequency and risk factors of endocrine complications in Turkish children and adolescents with sickle cell anemia. Turk J Hematol 2013;30:25-31.

Phillips G Jr., Becker B, Keller VA, Hartman J 4th. Hypothyroidism in adults with sickle cell anemia. Am J Med 1992;92:567-70.

Pi H, Rayner SG, Ralph DD, Nolley S, Barros LM, Steinberg ZL, et al. Thyroid-stimulating hormone and mortality in pulmonary arterial hypertension. BMJ Open Respira Res 2022;9:e001348.

Calissendorff J, Falhammar H. To treat or not to treat subclinical hypothyroidism, what is the evidence? Medicina (Kaunas) 2020;56:40.

Honsel V, Khimoud D, Ranque B, Offredo L, Joseph L, Pouchot J, et al. Comparison between adult patients with sickle cell disease of sub- Saharan African origin born in metropolitan France and in sub-Saharan Africa. J Clin Med 2019;8:2173.

El-Feki MA, Abdalla NH, Atta MI, Ibrahim AA. Serum level of thyroid hormones in patients with chronic hepatitis C virus infection. Open J Endocr Metab Dis 2016;6:126-34.

Hagag AA, El-Asy HM, Badraia IM, Hablas NM, El-Latif AE. Thyroid function in Egyptian children with sickle cell anemia in correlation with iron load. Endocr Metab Immune Disord Drug Targets 2019;19:46-52.

Garadah TS, Jaradat AA, Alalawi ME, Hassan AB. Hormonal and echocardiographic abnormalities in adult patients with sickle-cell anemia in Bahrain. J Blood Med 2016;7:283-9.

Chakravarthy V, Ejaz S. Thyroxine-binding globulin deficiency. In: StatPearls. Treasure Island, FL: StatPearls Publishing; 2022.

Published

07-07-2023

How to Cite

SWAIN, J., B. MOHANTY, N. kumar patel, and chakradhar majhi. “THYROID FUNCTION TEST IN SICKLE-CELL DISEASE”. Asian Journal of Pharmaceutical and Clinical Research, vol. 16, no. 7, July 2023, pp. 125-8, doi:10.22159/ajpcr.2023.v16i7.47607.

Issue

Section

Original Article(s)

Most read articles by the same author(s)