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The Relationship of 19 Functional Polymorphisms in Iodothyronine Deiodinase and Psychological Well-being in Hypothyroid Patients

Overview
Journal Endocrine
Specialty Endocrinology
Date 2017 May 4
PMID 28466400
Citations 9
Authors
Affiliations
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Abstract

Purpose: Levothyroxine supplementation is insufficient for the management of one tenth of patients with hypothyroidism. Iodothyronine deiodinases have been suggested to play a role in residual hypothyroid symptoms of these patients by controlling local thyroid hormone homeostasis. Previous research has suggested a relationship between commonly inherited variations in type 2 iodothyronine deiodinase and impaired well-being. We evaluated the prevalence of iodothyronine deiodinase genotypes and their association with psychological well-being in the Korean hypothyroid population.

Methods: A prospective observational study. We enrolled 196 hypothyroid subjects (136 chronic autoimmune thyroiditis and 60 thyroid cancer) and assessed baseline well-being using six validated questionnaires. Genotyping was conducted for 19 single nucleotide polymorphisms in type 1, 2, and 3 iodothyronine deiodinase using Sequenom MassARRAY matrix-assisted laser desorption/ionization time-of-flight mass spectrometry in all patients.

Results: Frequencies of iodothyronine deiodinase genotypes and well-being scores were not different in hypothyroid subjects according to their disease types. Minor genotypes of a few iodothyronine deiodinase 1 variants (rs11206244, rs2294512, and rs4926616) were associated with reduced psychological well-being. However, iodothyronine deiodinase 2 and 3 variants had no effect on baseline well-being.

Conclusion: Minor variations in iodothyronine deiodinase 1 were associated with decreased well-being in the Korean hypothyroid population, whereas iodothyronine deiodinase 2 and 3 were not. Due to controversial results among different ethnicities, further studies to clarify the effects of iodothyronine deiodinase polymorphisms on psychological well-being are warranted in hypothyroid individuals.

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References
1.
Philibert R, Beach S, Gunter T, Todorov A, Brody G, Vijayendran M . The relationship of deiodinase 1 genotype and thyroid function to lifetime history of major depression in three independent populations. Am J Med Genet B Neuropsychiatr Genet. 2011; 156B(5):593-9. PMC: 3236034. DOI: 10.1002/ajmg.b.31200. View

2.
He B, Li J, Wang G, Ju W, Lu Y, Shi Y . Association of genetic polymorphisms in the type II deiodinase gene with bipolar disorder in a subset of Chinese population. Prog Neuropsychopharmacol Biol Psychiatry. 2009; 33(6):986-90. DOI: 10.1016/j.pnpbp.2009.05.003. View

3.
Torlontano M, Durante C, Torrente I, Crocetti U, Augello G, Ronga G . Type 2 deiodinase polymorphism (threonine 92 alanine) predicts L-thyroxine dose to achieve target thyrotropin levels in thyroidectomized patients. J Clin Endocrinol Metab. 2007; 93(3):910-3. DOI: 10.1210/jc.2007-1067. View

4.
Saravanan P, Simmons D, Greenwood R, Peters T, Dayan C . Partial substitution of thyroxine (T4) with tri-iodothyronine in patients on T4 replacement therapy: results of a large community-based randomized controlled trial. J Clin Endocrinol Metab. 2004; 90(2):805-12. DOI: 10.1210/jc.2004-1672. View

5.
McAninch E, Jo S, Preite N, Farkas E, Mohacsik P, Fekete C . Prevalent polymorphism in thyroid hormone-activating enzyme leaves a genetic fingerprint that underlies associated clinical syndromes. J Clin Endocrinol Metab. 2015; 100(3):920-33. PMC: 4333048. DOI: 10.1210/jc.2014-4092. View