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Marco Bonomi, Maria Carla Proverbio, Giovanna Weber, Giuseppe Chiumello, Paolo Beck-Peccoz, Luca Persani, Hyperplastic Pituitary Gland, High Serum Glycoprotein Hormoneα -Subunit, and Variable Circulating Thyrotropin (TSH) Levels as Hallmark of Central Hypothyroidism due to Mutations of the TSHβ Gene, The Journal of Clinical Endocrinology & Metabolism, Volume 86, Issue 4, 1 April 2001, Pages 1600–1604, https://doi.org/10.1210/jcem.86.4.7411
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Inheritable isolated central hypothyroidism (ICH) due to mutations of TSHβ gene has been reported in few patients. For this reason the diagnostic criteria are vague. The disorder is usually characterized by undetectable TSH levels, although low/normal serum TSH, depending on TSH measurement methods, has been documented in some patients. Here we report an Egyptian girl with ICH due to a novel nonsense mutation of the TSHβ gene (Q49X). She was referred at 75 days of age for severe clinical signs of hypothyroidism, whose central origin was documented by normal serum TSH, low free T4 and free T3 levels, impaired TSH response to TRH, absence of 99Tc thyroidal uptake, and antithyroid autoantibodies. Ultrasound revealed a hypoplastic thyroid, whereas magnetic resonance imaging showed a hyperplastic pituitary. All other pituitary hormones, including PRL, were normally secreted. A diagnosis of idiopathic ICH was made, and substitutive l-T4 treatment was started at 81 days of age. At the age of 7 yr the patient had normal thyroid hormone levels, but was severely mentally retarded. Interestingly, the sella computed tomography scan had completely normalized. At 8 yr of age the patient was reinvestigated after 6-week l-T4 withdrawal. TSH values were highly variable depending on the measurement method used, whereas extremely high levels of circulating free glycoprotein α-subunit were recorded. Despite the fact that mutant TSHβ lacks 60% of the C-terminal amino acid sequence, it forms with the α-subunit a heterodimer with preserved immunoreactivity in some TSH measurement methods, but the mutant heterodimer is completely devoid of bioactivity. In conclusion, high circulating free glycoprotein α-subunit levels, variable TSH levels, and, possibly, hyperplastic pituitary gland are the hallmark of ICH due to mutations of the TSHβ gene.
