Literature DB >> 14669836

Resistance to thyrotropin.

S Refetoff1.   

Abstract

Resistance to TSH is a syndrome of reduced sensitivity to a biologically active TSH molecule. Subjects have elevated TSH levels but no goiter. However, thyroid hormone concentration may vary from normal to very high, depending on the severity of the resistance. Individuals with very high TSH, low T4 and hypoplastic thyroid glands can be mistakenly diagnosed as having primary hypothyroidism due to a defective development of the thyroid gland. Those with normal or slightly decreased T4 can be misdiagnosed as having central hypothyroidism especially if their serum TSH concentration is only slightly elevated. Mutations in the TSH receptor (TSHr) gene have been reported in 16 families with homozygous or compound heterozygous inheritance. The mutant TSHrs show reduced or no function due to either altered ligand binding or defect in membrane targeting. Some individuals, heretozygous for a TSHr gene mutation can present mild resistance to TSH manifesting as euthyroidism with slight hyperthyrotropinemia. A larger proportion of families express the phenotype of resistance to TSH in the absence of a TSHr defect. In many the inheritance is dominant and the genetic cause has not been yet determined.

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Year:  2003        PMID: 14669836     DOI: 10.1007/BF03347364

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  42 in total

1.  A novel mutation in the thyrotropin (TSH) receptor gene causing loss of TSH binding but constitutive receptor activation in a family with resistance to TSH.

Authors:  D Russo; C Betterle; F Arturi; E Chiefari; M E Girelli; S Filetti
Journal:  J Clin Endocrinol Metab       Date:  2000-11       Impact factor: 5.958

Review 2.  Molecular tinkering of G protein-coupled receptors: an evolutionary success.

Authors:  J Bockaert; J P Pin
Journal:  EMBO J       Date:  1999-04-01       Impact factor: 11.598

3.  Enhancer and promoter element interactions dictate cyclic adenosine monophosphate mediated and cell-specific expression of the glycoprotein hormone alpha-gene.

Authors:  J L Jameson; A C Powers; G D Gallagher; J F Habener
Journal:  Mol Endocrinol       Date:  1989-05

Review 4.  Neuroendocrine control of thyrotropin secretion.

Authors:  J E Morley
Journal:  Endocr Rev       Date:  1981       Impact factor: 19.871

Review 5.  Thyroid-specific gene expression.

Authors:  G Damante; R Di Lauro
Journal:  Biochim Biophys Acta       Date:  1994-08-02

6.  Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodystrophy in six kindreds.

Authors:  M A Levine; T S Jap; R S Mauseth; R W Downs; A M Spiegel
Journal:  J Clin Endocrinol Metab       Date:  1986-03       Impact factor: 5.958

7.  Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: evidence for a new inactivating mutation of the TSH receptor gene.

Authors:  M Tonacchera; P Agretti; A Pinchera; V Rosellini; A Perri; P Collecchi; P Vitti; L Chiovato
Journal:  J Clin Endocrinol Metab       Date:  2000-03       Impact factor: 5.958

8.  Imparied cyclic-AMP response to thyrotrophin in congenital hypothyroidism with thyroglobulin deficiency.

Authors:  G A Medeiros-Neto; M Knobel; M D Bronstein; J Simonetti; F F Filho; E Mattar
Journal:  Acta Endocrinol (Copenh)       Date:  1979-09

9.  Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism.

Authors:  Luisella Alberti; Maria Carla Proverbio; Sabine Costagliola; Roberto Romoli; Benedetta Boldrighini; Maria Cristina Vigone; Giovanna Weber; Giuseppe Chiumello; Paolo Beck-Peccoz; Luca Persani
Journal:  J Clin Endocrinol Metab       Date:  2002-06       Impact factor: 5.958

Review 10.  Familial unresponsiveness to thyrotropin by autosomal recessive inheritance.

Authors:  J Takamatsu; M Nishikawa; M Horimoto; N Ohsawa
Journal:  J Clin Endocrinol Metab       Date:  1993-12       Impact factor: 5.958

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  16 in total

1.  Consecutive mutational events in a TSHR allele of Arab families with resistance to thyroid stimulating hormone.

Authors:  Chutintorn Sriphrapradang; Alina German; Alexandra M Dumitrescu; Samuel Refetoff
Journal:  Thyroid       Date:  2012-02-07       Impact factor: 6.568

Review 2.  Role and Mechanisms of Actions of Thyroid Hormone on the Skeletal Development.

Authors:  Ha-Young Kim; Subburaman Mohan
Journal:  Bone Res       Date:  2013-06-28       Impact factor: 13.567

Review 3.  Detection and treatment of congenital hypothyroidism.

Authors:  Annette Grüters; Heiko Krude
Journal:  Nat Rev Endocrinol       Date:  2011-10-18       Impact factor: 43.330

4.  The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation.

Authors:  Chutintorn Sriphrapradang; Yardena Tenenbaum-Rakover; Mia Weiss; Marla S Barkoff; Osnat Admoni; Dallasheh Kawthar; Gianluigi Caltabiano; Leonardo Pardo; Alexandra M Dumitrescu; Samuel Refetoff
Journal:  J Clin Endocrinol Metab       Date:  2011-04-13       Impact factor: 5.958

Review 5.  The molecular causes of thyroid dysgenesis: a systematic review.

Authors:  I C Nettore; V Cacace; C De Fusco; A Colao; P E Macchia
Journal:  J Endocrinol Invest       Date:  2013-05-22       Impact factor: 4.256

Review 6.  Update in TSH receptor agonists and antagonists.

Authors:  Marvin C Gershengorn; Susanne Neumann
Journal:  J Clin Endocrinol Metab       Date:  2012-09-27       Impact factor: 5.958

7.  Long-term outcome of loss-of-function mutations in thyrotropin receptor gene.

Authors:  Yardena Tenenbaum-Rakover; Shlomo Almashanu; Ora Hess; Osnat Admoni; Ahmad Hag-Dahood Mahameed; Naama Schwartz; Stavit Allon-Shalev; Dani Bercovich; Samuell Refetoff
Journal:  Thyroid       Date:  2015-01-28       Impact factor: 6.568

Review 8.  Thyrotropin receptor-associated diseases: from adenomata to Graves disease.

Authors:  Terry F Davies; Takao Ando; Reigh-Yi Lin; Yaron Tomer; Rauf Latif
Journal:  J Clin Invest       Date:  2005-08       Impact factor: 14.808

9.  Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children.

Authors:  F Teofoli; M Camilot; L Tatò
Journal:  J Endocrinol Invest       Date:  2007-02       Impact factor: 4.256

10.  Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism.

Authors:  P Agretti; G De Marco; C Di Cosmo; B Bagattini; E Ferrarini; L Montanelli; P Vitti; M Tonacchera
Journal:  J Endocrinol Invest       Date:  2014-01-09       Impact factor: 4.256

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