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Resistance to Thyroid Hormone

  • Chapter
Diseases of the Thyroid

Part of the book series: Contemporary Endocrinology ((COE,volume 2))

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Abstract

The concept of a hormone-resistant disease has been introduced around the 1940s by Fuller Albright by studying the rickets resistant to Vitamin D therapy and the “Pseudohypoparathyroidism—an example of Seabright-Bantam syndrome” (1,2).He called the disease “pseudo,” as the patients showed clinical features of hypoparathyroidism, but the injection of parathyroid hormone was not followed by the expected increases of serum calcium levels and urinary phosphate excretion. Thus, the term “pseudo” entered into the medical vocabulary to indicate an endocrine disorder resembling a known disease, but accompanied by failure of the end-organ to respond to the specific hormone. Several examples of insensitivity to many hormones, including insulin, corticosteroids, androgens, estrogens, anterior and posterior pituitary hormones, have been reported in the last 50 yr. Moreover, it is now clearly demonstrated that genetic mutations of hormone receptor proteins or proteins involved in the signal transduction are the underlying cause of most clinical conditions that we prefer today to call not “pseudo,” but “resistance to thyroid hormone action.”

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References

  1. Albright F, Butler AM, Bloombreg E. Rickets resistant to vitamin D therapy. Am J Dis Child 1937; 54: 531–547.

    Google Scholar 

  2. Albright F, Burnett CH, Smith PH, Parson W. Pseudohypoparathyroidism—an example of “Seabright-Bantam syndrome”. Endocrinology 1942; 30: 922–932.

    CAS  Google Scholar 

  3. Sunthornthepvarakul T, Gottschalk ME, Hayashi Y, Refetoff S. Resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene. N Engl J Med 1995; 332: 155–160.

    CAS  Google Scholar 

  4. Refetoff S, DeWind LT, DeGroot LJ. Familial syndrome combining deaf-mutism, stippled epiphyses, goiter and abnormally high PBI: possible target organ refractoriness to thyroid hormone. J Clin Endocr 1967; 27: 279–294.

    PubMed  CAS  Google Scholar 

  5. Lamberg BA. Congenital euthyroid goiter and partial peripheral resistance to thyroid hormones. Lancet 1973; 1: 854–857.

    PubMed  CAS  Google Scholar 

  6. Lamberg BA, Sandström R, Rosengârd, Säarinen P, Evered DC. Sporadic and familial partial peripheral resistance to thyroid hormone. In: Harland WA, Orr JS eds. Thyroid hormone metabolism. Academic, London, 1975, pp. 139–161.

    Google Scholar 

  7. Bode HH, Danon M, Weintraub BD, Maloof F, Crawford JD. Partial target organ resistance to thyroid hormone. J Clin Invest 1973; 52: 776–782.

    PubMed  CAS  Google Scholar 

  8. Agerbaek H. Congenital goiter presumably resulting from tissue resistance to thyroid hormones. Israel J Med Sci 1973; 52: 1859, 1860.

    Google Scholar 

  9. Schneider G, Keiser HR, Bardin CW. Peripheral resistance to thyroxine: a cause of short stature in a boy without goiter. Clin Endocrinol (Oxf) 1975; 4: 111–118.

    CAS  Google Scholar 

  10. Gershengorn MC, Weintraub BD. Thyrotropin-induced hyperthyroidism caused by selective pituitary resistance to thyroid hormone: a new syndrome of “inappropriate secretion of TSH” J Clin Invest 1975; 56: 633–642.

    PubMed  CAS  Google Scholar 

  11. Faglia G, Beck-Peccoz P, Piscitelli G, Medri G. Inappropriate secretion of thyrotropin by the pituitary. Horm Res 1987; 26: 79–99.

    PubMed  CAS  Google Scholar 

  12. Kaplan MM, Swartz SL, Larsen PR. Partial peripheral resistance to thyroid hormone. Am J Med 1981; 70: 1115–1121.

    PubMed  CAS  Google Scholar 

  13. Refetoff S. Syndrome to thyroid hormone resistance. Am J Physiol 1982; 243: E88–E98.

    PubMed  CAS  Google Scholar 

  14. Refetoff S, Weiss RE, Usala S. The syndromes of resistance to thyroid hormone. Endocr Rev 1993; 14: 384–399.

    Google Scholar 

  15. Lamberg BA, Rosengard S, Liewendahl K, Saarinen P, Evered DC. Familial partial peripheral resistance to thyroid hormones. Acta Endocrinol (Copenh) 1978; 87: 303–312.

    CAS  Google Scholar 

  16. Elewaut A, Mussche M, Vermeulen A. Familial partial target organ resistance to thyroid hormone. J Clin Endocrinol Metab 1976; 43: 575–581.

    PubMed  CAS  Google Scholar 

  17. Novogroder M, Utiger R, Boyar R, Levine LS. Juvenile hyperthyroidism with elevated thyrotropin (TSH) and normal 24-hour FSH, LH, GH and prolactin secretory patterns. J Clin Endocrinol Metab 1977; 45: 1053–1059.

    Google Scholar 

  18. Tamagna EI, Carlson HE, Hershman JM, Reed AW. Pituitary and peripheral resistance to thyroid hormone. Clin Endocrinol (Oxf) 1979; 10: 431–441.

    CAS  Google Scholar 

  19. Refetoff S, DeGroot LJ, Barsano CP. Defective thyroid hormone feedback regulation in the syndrome of peripheral resistance to thyroid hormone. J Clin Endocrinol Metab 1980; 51: 41–45.

    PubMed  CAS  Google Scholar 

  20. Vandalem JL, Pirens G, Hennen G. Familial inappropriate TSH secretion: evidence suggesting a dissociated pituitary resistance to T3 and T4. J Endocrinol Invest 1981; 4: 413–422.

    PubMed  CAS  Google Scholar 

  21. Brooks MH, Barbato AT, Collins S, Garbincius J, Neidballa RG, Hoffman D. Familial thyroid hormone resistance. Am J Med 1981; 71: 414–421.

    PubMed  CAS  Google Scholar 

  22. Linde R, Alexander N, Island DP, Rabin D. Familial insensitivity of pituitary and periphery tissue to thyroid hormone: a case report in two generations and a review of the literature. Metabolism 1982; 31: 510–513.

    PubMed  CAS  Google Scholar 

  23. Bantle JP, Seeling S, Mariash CN, Ulstrom RA, Oppenheimer JH. Resistance to thyroid hormones: a disorder frequently confused with Graves’ disease. Arch Intern Med 1982; 142: 1867–1871.

    PubMed  CAS  Google Scholar 

  24. Rösler A, Litvin Y, Hage C, Gross J, Cerasi E. Familial hyperthyroidism due to inappropriate thyrotropin secretion successfully treated with triiodothyronine. J Clin Endocrinol Metab 1982; 54: 76–82.

    PubMed  Google Scholar 

  25. Spanheimer RG, Bar RS, Hayford JC. Hyperthyroidism caused by inappropriate thyrotropin secretion. Arch Intern Med 1982; 142: 1283–1289.

    PubMed  CAS  Google Scholar 

  26. Gharib H, Carpenter PC, Scheithauer BW, Service FJ. The spectrum of inappropriate pituitary thyrotropin secretion associated with hyperthyroidism. Mayo Clin Proc 1982; 57: 556–563.

    PubMed  CAS  Google Scholar 

  27. Cooper DS, Ladenson PW, Nisula BC, Dunn JF, Chapman EM, Ridgway EC. Familial thyroid hormone resistance. Metabolism 1982; 31: 504–509.

    PubMed  CAS  Google Scholar 

  28. Refetoff S, Salazar A, Smith TJ, Scherberger NH. The consequences of in appropriate treatment because of failure to recognize the syndrome of pituitary and peripheral tissue resistance to thyroid hormone. Metabolism 1983; 32: 822–834.

    PubMed  CAS  Google Scholar 

  29. Pagliara AS, Caplan RH, Gundersen CB, Wickus GG, Elston III ACV. Peripheral resistance to thyroid hormone in a family: heterogeneity of clinical presentation. J Pediatr 1983; 103: 228–234.

    PubMed  CAS  Google Scholar 

  30. Takamatsu J, Majima M, Miki K, Kuma K, Mozai T. Serum ferritin as a marker of thyroid hormone action on peripheral tissues. J Clin Endocrinol Metab 1985; 61: 672–676.

    PubMed  CAS  Google Scholar 

  31. Magner JA, Petrick P, Menezes-Ferreira MM, Stelling M, Weintraub BD. Familial generalized resistance of thyroid hormones: report of three kindreds and correlation of patterns of affected tissues with the binding of [125I]triiodothyronine to fibroblast nuclei. J Endocrinol Invest 1986; 9: 459–469.

    PubMed  CAS  Google Scholar 

  32. Hopwood NJ, Sauder SE, Shapiro B, Sisson JC. Familial partial peripheral and pituitary resistance to thyroid hormone: a frequently missed diagnosis? Pediatrics 1986; 78: 1114–1122.

    PubMed  CAS  Google Scholar 

  33. Hughes IA, Ichikawa K, DeGroot LJ, John R, Jones MK, Hall R, Scanlon MF. Non-adenomatous inappropriate TSH hypersecretion and euthyroidism requires no treatment. Clin Endocrinol (Oxf) 1987; 27: 475–483.

    CAS  Google Scholar 

  34. Smallridge RC, Parker RA, Wiggs EA, Rajagopal KR, Fein HG. Thyroid hormone resistance in a large kindred: physiologic, biochemical, pharmacologic and neuropsychologic studies. Am J Med 1989; 86: 289–296.

    PubMed  CAS  Google Scholar 

  35. Refetoff S, DeGroot LJ, Benard B, DeWind LT. Studies of a sibship with apparent hereditary resistance to the intracellular action of thyroid hormone. Metabolism 1972; 21: 723–756.

    PubMed  CAS  Google Scholar 

  36. Crino A, Borrelli P, Salvatori R, Cortelazzi D, Roncoroni R, Beck-Peccoz P. Anti-iodothyronine autoantibodies in a girl with hyperthyroidism due to pituitary resistance to thyroid hormones. J Endocrinol Invest 1992; 15: 113–120.

    PubMed  CAS  Google Scholar 

  37. Connel JMC, McCruden DC, Davies DL, Alexander WD. Bromocriptine for inappropriate thyrotropin secretion. Ann Intern Med 1982; 96: 251–252.

    Google Scholar 

  38. Beck-Peccoz P, Piscitelli G, Cattaneo MG, Faglia G. Successful treatment of hyperthyroidism due to nonneoplastic pituitary TSH hypersecretion with 3,5,3 ’-triiodothyroacetic acid (TRIAC). J Endocrinol Invest 1983; 6: 217–223.

    PubMed  CAS  Google Scholar 

  39. Sriwatanakul K, McCormick K, Woolf P. Thyrotropin (TSH)-induced hyperthyroidism: response of TSH to dopamine and its agonists. J Clin Endocrinol Metab 1984; 58: 255–261.

    PubMed  CAS  Google Scholar 

  40. Takamatsu J, Mozai T, Kuma K. Bromocriptine therapy for hyperthyroidism due to increased thyrotropin secretion. J Clin Endocrinol Metab 1984; 58: 934–936.

    PubMed  CAS  Google Scholar 

  41. Drucker D, Josse R. Inappropriate TSH secretion with abnormal thyrotroph sensitivity to dopamine. Clin Invest Med 1985; 8: 117–120.

    PubMed  CAS  Google Scholar 

  42. Williams G, Kraenzlin M, Sandler L, Burrin J, Law A, Bloom S, Joplin GF. Hyperthyroidism due to non-tumoural inappropriate TSH secretion: effects of a long-acting somatostatin analogue (SMS 201–995). Acta Endocrinol (Copenh) 1986; 113: 42–46.

    CAS  Google Scholar 

  43. Hamon P, Bovier-Lapierre M, Robert M, Peynaud D, Pugeat M, Orgiazzi J. Hyperthyroidism due to selective pituitary resistance to thyroid hormones in a 15-month-old boy: efficacy of D-thyroxine therapy. J Clin Endocrinol Metab 1988; 67: 1089–1093.

    PubMed  CAS  Google Scholar 

  44. Salmela PI, Wide L, Juustila H, Ruokonen A. Effects of thyroid hormones (T4, T3), bromocriptine and TRIAC on inappropriate TSH hypersecretion. Clin Endocrinol (Oxf) 1988; 28: 497–507.

    CAS  Google Scholar 

  45. Beck-Peccoz P, Mariotti S, Guillausseau PJ, Medri G, Piscitelli G, Bertoli A, Barbarino A, Rondena M, Chanson P, Pinchera A, Faglia G. Treatment of hyperthyroidism due to inappropriate secretion of thyrotropin with the somatostatin analog SMS 201–995. J Clin Endocrinol Metab 1989; 68: 208–214.

    PubMed  CAS  Google Scholar 

  46. Dorey F, Strauch G, Gayno JP. Thyrotoxicosis due to pituitary resistance to thyroid hormones. Successful control with D-thyroxine: a study in three patients. Clin Endocrinol (0x0. 1990; 32: 221–227.

    CAS  Google Scholar 

  47. Aguilar Diosdado M, Escobar-Jimenez L, Fernandez Soto ML, Garcia Curiel A, Escobar-Jimenez F. Hyperthyroidism due to a familial pituitary resistance to thyroid hormone: success-ful control with 3,5,3 ’-triiodothyroacetic associated to propranolol. J Endocrinol Invest 1991; 14: 663–668.

    Google Scholar 

  48. Kourides IA, Ridgway EC, Weintraub BD, Bigos ST, Gershengorn MC, Maloof F. Thyrotropin-induced hyperthyroidism: use of alpha and beta subunit levels to identify patients with pituitary tumors. J Clin Endocrinol Metab 1977; 45: 534–543.

    PubMed  CAS  Google Scholar 

  49. Beck-Peccoz P, Roncoroni R, Mariotti S, Medri G, Marcocci C, Brabant G, Forloni F, Pinchera A, Faglia G. Sex hormone-binding globulin measurement in patients with inappropriate secretion of thyrotropin (IST): evidence against selective pituitary thyroid hormone resistance in nonneoplastic IST. J Clin Endocrinol Metab 1990; 71: 19–25.

    PubMed  CAS  Google Scholar 

  50. Beck-Peccoz P, Persani L, Faglia G. Glycoprotein hormone a-subunit in pituitary adenomas. Trends Endocrinol Metab 1992; 3: 41–45.

    PubMed  CAS  Google Scholar 

  51. Wortsman J, Premachandra BN, Williams K, Burman KD, Hay ID, Davis PJ. Familial resistance to thyroid hormone associated with decrease transport across the plasma membrane. Ann Intern Med 1983; 98: 904–909.

    PubMed  CAS  Google Scholar 

  52. Refetoff S, Matalon R, Bigazzi M. Metabolism of L-thyroxine (T4) and L-triiodothyronine (T3) by human fibroblasts in tissue culture: evidence for cellular binding proteins and conversion of T4 to T3. Endocrinology 1972; 91: 934–947.

    PubMed  CAS  Google Scholar 

  53. Holm AC, Kagedal B. Kinetics of triiodothyronine uptake by erythrocytes in hyperthyroidism, hypothyroidism and thyroid hormone resistance. J Clin Endocrinol Metab 1989; 69: 364–368.

    PubMed  CAS  Google Scholar 

  54. Oppenheimer JH, Koerner D, Schwartz HL, Surks M. Specific-nuclear triiodothyronine binding sites in a rat liver and kidney. J Clin Endocrinol Metab 1972; 35: 330–333.

    PubMed  CAS  Google Scholar 

  55. Bernal J, Refetoff S, DeGroot LJ. Abnormalities of triiodothyronine binding to lymphocyte and fibroblast nuclei from a patient with peripheral resistance to thyroid hormone action. J Clin Endocrinol Metab 1978; 47: 1266–1272.

    PubMed  CAS  Google Scholar 

  56. Eil C, Fein HG, Smith TJ, Furlanetto RW, Bourgeois M, Stelling MW, Weintraub BD. Nuclear binding of [125I] triiodothyronine in dispersed cultured skin fibroblasts from patients with resistance to thyroid hormone. J Clin Endocrinol Metab 1982; 57: 502–510.

    Google Scholar 

  57. Menezes-Ferreira MM, Eil C, Wortsman J, Weintraub BD. Decrease nuclear uptake of [125I] triiodo-L-thyronine in fibroblasts from patients with peripheral thyroid hormone resistance. J Clin Endocrinol Metab 1984; 59: 1081–1087.

    PubMed  CAS  Google Scholar 

  58. Ichikawa K, Hughes IA, Horwitz AL, DeGroot LJ. Characterization of nuclear thyroid hormone receptors of cultured skin fibroblasts from patients with resistance to thyroid hormone. Metabolism 1987; 36: 392–399.

    PubMed  CAS  Google Scholar 

  59. Chait A, Kanter R, Green W, Kenny M. Defective thyroid hormone action in fibroblasts cultured from subjects with the syndrome of resistance to thyroid hormones. J Clin Endocrinol Metab 1982; 54: 767–772.

    PubMed  CAS  Google Scholar 

  60. Murata Y, Refetoff S, Horwitz AL, Smith TJ. Hormonal regulation of glycosaminoglycan accumulation in fibroblasts from patients with resistance to thyroid hormone. J Clin Endocrinol Metab 1983; 57: 1233–1239.

    PubMed  CAS  Google Scholar 

  61. Ceccarelli P, Refetoff S, Murata Y. Resistance to thyroid hormone diagnosed by the reduced response of fibroblasts to the triiodothyronine induced suppression of fibronectin synthesis. J Clin Endocrinol Metab 1987; 65: 242–246.

    PubMed  CAS  Google Scholar 

  62. Galli G, Tanini A, Toccafondi R. Triiodothyronine and growth rate of fibroblasts from patients with generalized resistance to thyroid hormone. Ann Endocrinol (Paris) 1988; 49: 189 (Abstract).

    Google Scholar 

  63. Sap J, Munoz A, Damm K, Goldberg Y, Ghysdael J, Lentz A, Beng H, Vennström B. The c-erbA proteins is a high-affinity receptor for thyroid hormone. Nature 1986; 324: 635–640.

    PubMed  CAS  Google Scholar 

  64. Weinberger C, Thompson CC, Ong ES, Lebo R, Gruol DJ, Evans RM. The c-erbA gene encodes a thyroid hormone receptor. Nature 1986; 324: 641–646.

    PubMed  CAS  Google Scholar 

  65. Evans R. The steroid and thyroid hormone receptor superfamily Science 1988; 240: 889–895.

    CAS  Google Scholar 

  66. Lazar MA, Chin WW. Nuclear thyroid hormone receptors. J Clin Invest 1990; 86: 1777–1782.

    PubMed  CAS  Google Scholar 

  67. Lazar MA. Thyroid hormone receptors: multiple forms, multiple possibilities. Endocr Rev 1993; 14: 184–193.

    PubMed  CAS  Google Scholar 

  68. Nakai A, Seino S, Sakurai A, Szilak I, Bell GI, DeGroot LJ. Characterization of a thyroid hor-mone receptor expressed in human kidney and other tissues. Proc Nati Acad Sci USA 1988; 85: 2781–2785.

    CAS  Google Scholar 

  69. Schwartz HL, Lazar MA, Oppenheimer JH. Widespread distribution of immunoreactive thyroid hormone 02 receptor (TRß2) in the nuclei of extapituitary rat tissues. J. Biol. Chem 1994;269:24, 777–24, 782.

    Google Scholar 

  70. Darling DS, Beebe JS, Burnside J, Winslow ER, Chin WW. 3,5,3 ’-triiodothyronine (T3) receptor-auxiliary protein (TRAP) binds DNA and forms heterodimers with the T3 receptor. Mol Endocrinol 1991; 5: 73–84.

    PubMed  CAS  Google Scholar 

  71. Graupner G, Wills KN, Tzukerman M, Zhang KK, Pfahl M. Thyroid hormone receptors repress estrogen receptor activation of a TRE. Mol Endocrinol 1991; 5: 365–372.

    PubMed  CAS  Google Scholar 

  72. Chin WW, Yen PM. T3 or not T3: the slings and arrows of outrageous TR function. Endocrinology 1996; 137: 387–389.

    PubMed  CAS  Google Scholar 

  73. Horlein AJ, Naar A, Heinzel T, Torchia J, Gloss B, Kurokawa R, Ryan A, Kamei Y, Soderstrom M, Glass CK, Rosenfeld MG. Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor. Nature 1995; 377: 397–404.

    PubMed  CAS  Google Scholar 

  74. Takeshita A, Yen PM, Misiti S, Cardona GR, Liu Y, Chin WW. Molecular cloning and properties of a full-length putative thyroid hormone receptor coactivator. Endocrinology 1996; 137: 3594–3597.

    PubMed  CAS  Google Scholar 

  75. Usala SJ, Bale AE, Gesundheit N, Weinberger C, Lash RW, Wondisford FE, McBride OW, Weintraub BD. Tight linkage between the syndrome of generalized thyroid hormone resistance and the human c-erbAß gene. Mol Endocrinol 1988; 2: 1217–1220.

    PubMed  CAS  Google Scholar 

  76. Sakurai A, Takeda K, Ain K, Ceccarelli P, Nakai A, Seino S, Bell GI, Refetoff S, DeGroot LJ. Generalized resistance to thyroid hormone associated with a mutation in the ligand-binding domain of the human thyroid hormone receptor ß. Proc Natl Acad Sci USA 1989; 86: 8977–8981.

    PubMed  CAS  Google Scholar 

  77. Usala SJ, Tennyson GE, Bale AE, Lash RW, Gesundheit N, Wondisford FE, Accili D, Hauser P, Weintraub BD. A base mutation of the c-erbAß thyroid hormone receptor in a kindred with generalized thyroid hormone resistance. Molecular heterogeneity in two other kindreds. J Clin Invest 1990; 85: 93–100.

    PubMed  CAS  Google Scholar 

  78. Announcement. A registry for resistance to thyroid hormone resistance. Mol Endocrinol 1994; 8: 1558.

    Google Scholar 

  79. Takeda K, Weiss RE, Refetoff S. Rapid localization of mutations in the thyroid hormone receptor ß gene by denaturing gradient ge electrophoresis in eighteen families with thyroid hormone resistance. J Clin Endocrinol Metab 1992; 74: 712–719.

    PubMed  CAS  Google Scholar 

  80. Beck-Peccoz P, Chatterjee VKK, Chin WW, DeGroot LJ, Jameson JL, Nakamura H, Refetoff S, Usala SJ, Weintraub BD. Nomenclature of thyroid hormone receptor ß-gene mutations in resistance to thyroid hormone: consensus statement from the First Workshop on Thyroid Hormone Resistance, July 10–11, 1993, Cambridge, United Kingdom. J Clin Endocrinol Metab 1994; 78: 990–993.

    PubMed  CAS  Google Scholar 

  81. Adams M, Matthews C, Colllingwood TN, Tone Y, Beck-Peccoz P, Chatterjee VKK. Genetic analysis of 29 kindreds with generalized and pituitary resistence to thyroid hormone. Identification of thirteen novel mutations in the hormone receptor ß gene. J Clin Invest 1994; 94: 506–515.

    PubMed  CAS  Google Scholar 

  82. Hayashi Y, Sunthornthepvarakul T, Refetoff S. Mutations of CpG dinucleotides located in the triiodothyronine (T3)-binding domain of the thyroid hormone receptor (TR) ß gene that appears to be devoid of natural mutations may not be detected because they are unlikely to produce the clinical phenotype of resistance to thyroid hormone. J Clin Invest 1994; 94: 607–615.

    PubMed  CAS  Google Scholar 

  83. Nakamura H, Miyoshi Y, Sasaki S, Tagami T, Nakao K, Taniyama M, Yoshimi T. Comparison among three truncated T3 receptors identified in patients with generalized thyroid hormone resistance (GRTH). Thyroid 1994;4(Supp1.1):S-73(Abstract).

    Google Scholar 

  84. Groenhout EG, Dorin RI. Generalized thyroid hormone resistance due to a deletion of the car-boxy terminus of the c-erbAß receptor. Mol Cell Endocrinol 1994; 99: 81–86.

    PubMed  CAS  Google Scholar 

  85. Parrilla R, Mixon AJ, McPherson JA, McClaskey JH, Weintraub BD. Characterization of seven novel mutations of the c-erbAß gene in unrelated kindreds with generalized thyroid hor-mone resistance. Evidence of two “hot spot” regions of the ligand binding domain. J Clin Invest 1991; 88: 2123–2130.

    PubMed  CAS  Google Scholar 

  86. Usala SJ, Menke JB, Watson TL, Wondisford FE, Weintraub BD, Brard J, Bradle WEC, Ono S, Mueller OT, Bercu BB. A homozygous deletion in the c-erbAß thyroid hormone receptor gene in a patient with generalized thyroid hormone resistance: isolation and characterization of the mutant receptor. Mol Endocrinol 1991; 5: 327–335.

    PubMed  CAS  Google Scholar 

  87. Weiss RE, Weinberg M, Refetoff S. Identical mutations in unrelated families with generalized resistance to thyroid hormone occur in cytosine-guanine-rich areas of the thyroid hormone receptor beta gene. J Clin Invest 1993; 91: 2408–2415.

    PubMed  CAS  Google Scholar 

  88. Cooper DN, Yousoufian M. The CpG dinucleotide and human genetic disease. Hum Genet 1988; 78: 151–155.

    PubMed  CAS  Google Scholar 

  89. Ono S, Schwartz I, Mueller O, Root A, Usala S, Bercu B. Homozygosity for a dominant negative thyroid hormone receptor gene responsible for generalized thyroid hormone resistance. J Clin Endocrinol Metab 1991; 73: 990–994.

    PubMed  CAS  Google Scholar 

  90. Takeda K, Sakurai A, DeGroot LJ, Refetoff S. Recessive inheritance of thyroid hormone resistance caused by complete deletion of the protein-coding region of the thyroid hormone receptor-0 gene. J Clin Endocrinol Metab 1992; 74: 49–55.

    PubMed  CAS  Google Scholar 

  91. Mixson AJ, Renault JC, Ransom S, Bodenner DL, Weintraub BD. Identification of a novel mutation in the gene encoding the ß-triiodothyronine receptor in a patient with apparent selective pituitary resistance to thyroid hormone. Clin Endocrinol (Oxf) 1993; 38; 227–234.

    CAS  Google Scholar 

  92. Sasaki S, Nakamura H, Tagami T, Miyoshi Y, Nogimori T, Mitsuma T, Imura H. Pituitary resistance to thyroid hormone associated with a base mutation in the hormone binding domain of the human 3,5,3 ’-triiodothyroinine receptor beta. J Clin Endocrinol Metab 1993; 76: 1254–1258.

    PubMed  CAS  Google Scholar 

  93. Behr M, Loos U. 1992. A point mutation (Ala 229 to Thr) in the hinge domain of the c-erbAß thyroid hormone receptor gene in a family with generalised thyroid hormone resistance syndrome. Mol Endocrinol 1992; 6: 1119–1126.

    Google Scholar 

  94. Geffner ME, Su F, Ross NS, Hershman JM, Van Dop C, Menke JB, Hao E, Stanzak RK, Eaton T, Samuels HH, Usala S. An arginine to histidine mutation in codon 311 of the c-erbAß gene results in a mutant thyroid hormone receptor that does not mediate a dominant negative phenotype. J Clin Invest 1993; 91: 538–546.

    PubMed  CAS  Google Scholar 

  95. Burman K, Djuh Y, Nicholson D, Rhooms P, Wartofsky L, Fein H, Usala S, Hao E, Bradley W, Berard J, Smallridge R. Generalized thyroid hormone resistance: identification of an arginine to cystine mutation in codon 315 of the c-erbAß thyroid hormone receptor. J Endocrinol Invest 1992; 15: 573–579.

    PubMed  CAS  Google Scholar 

  96. Cugini CJ, Leidy J, Chertow B, Brard J, Bradley E, Menke J, Hao E, Usala S. An arginine to histidine mutation in codon 315 of the c-erbAß thyroid hormone receptor in a kindred with generalized resistance to thyroid hormone results in a receptor with significant 3,5,3 ’-triiodothyronine binding activity. J Clin Endocrinol Metab 1992; 74: 1164–1170.

    PubMed  CAS  Google Scholar 

  97. Adams M, Nagaya T, Tone Y, Jameson JL, Chatterjee VK. Functional properties of a novel mutant thyroid hormone receptor in a family with generalised thyroid hormone resistance syndrome. Clin Endocrinol (Oxf) 1992; 36: 281–289.

    CAS  Google Scholar 

  98. Boothroyd C, Hayward N, Hickman P, Ward G, Cameron D. Single base mutation in the hormone binding domain of the thyroid hormone receptor ß gene in generalized thyroid hormone resistance demonstrated by single stranded conformation polymorphism analysis. Biochem Biophys Res Comm 1991; 178: 606–612.

    PubMed  CAS  Google Scholar 

  99. Sasaki S, Nakamura H, Tagami T, Miyoshi Y, Tanaka K, Imura H. A point mutation of the T3 receptor ßl gene in a kindred of generalized resistance to thyroid hormone. Mol Cell Endocrinol 1992; 84: 159–166.

    PubMed  CAS  Google Scholar 

  100. Weiss RE, Chyna B, Duell PB, Hayashi Y, Sunthornthepvarakul T, Refetoff S 1994 A point mutation (C446R) in the thyroid hormone receptor-0 gene of a family with resistance to thyroid hormone. J Clin Endocrinol Metab 1994; 78: 1253–1256.

    Google Scholar 

  101. Refetoff S, Weiss RE, Wing JR. Resistance to thyroid hormone in subjects from two unrelated families is associated with a point mutation in the thyroid hormone receptor ß gene resulting in a replacement of the normal proline 453 with serine. Thyroid 1994; 4: 249–253.

    PubMed  CAS  Google Scholar 

  102. Shuto Y, Wakabayashi I, Amuro N, Minami S, Okazaki T. A point mutation in the 3,5,3 ’-triiodothyronine-binding domain of thyroid hormone receptor-ß associated with a family with generalized resistance to thyroid hormone. J Clin Endocrinol Metab 1992; 75: 213–217.

    PubMed  CAS  Google Scholar 

  103. Collingwood TN, Adams M, Tone Y, Chatterjee VKK. Spectrum of transcriptional, dimerization, and dominant negative properties of twenty different mutant thyroid hormone beta-receptors in thyroid hormone resistance syndrome. Mol Endocrinol 1994; 8: 1262–1277.

    PubMed  CAS  Google Scholar 

  104. Tsukagushi H, Yoshimasa Y, Fujimoto K, Ishii H, Yamamoto T, Yoshimasa T, Yagura T, Takamatsu J. Three novel mutations of thyroid hormone receptor ß gene in unrelated patients with resistance to thyroid hormone: two mutations of the same codon (H435L and H435Q) produce separate subtypes of resistance. J Clin Endocrinol Metab 1995; 80: 3613–3616.

    Google Scholar 

  105. Flynn T, Hollenberg A, Cohen O, Menke J, Usala S, Tollin S, Hegarty M, Wondisford EF. A novel C-terminal domain in the thyroid hormone receptor selectively mediates thyroid hormone inhibition. J Biol Chem 1994;269:32, 713–32, 716.

    Google Scholar 

  106. Chatterjee VKK, Nagaya T, Madison L, Datta S, Rentoumis A, Jameson J. Thyroid hormone resistance syndrome. Inhibition of normal receptor function by mutant thyroid hormone receptors. J Clin Invest 1991; 87: 1977–1984.

    PubMed  CAS  Google Scholar 

  107. Meier CA, Dickstein BM, Ashizawa K, McClaskey JH, Muchmore P, Ransom S C, Menke JB, Hao EH, Usala SJ, Bercu BB, Cheng SY, Weintraub BD. Variable transcriptional activity and ligand binding of mutant 01 3,3,3’-triiodothyronine receptors from four families with generalised resistance to thyroid hormone. Mol Endocrinol 1992; 6: 248–258.

    PubMed  CAS  Google Scholar 

  108. Nagaya T, Madison LD, Jameson JL. Thyroid hormone resistance mutants that cause resistance to thyroid hormone. Evidence for receptor competition for DNA sequences in target genes. J Biol Chem 1992;267:13, 014–13, 019.

    Google Scholar 

  109. Liu RT, Suzuki S, Takeda T, DeGroot LJ. An artificial thyroid hormone receptor mutant without DNA binding can have dominant negative effect. Mol Cell Endocrinol 1996; 120: 85–93.

    PubMed  CAS  Google Scholar 

  110. Chatterjee VKK, Beck-Peccoz P. Thyroid hormone resistance. Bailliére Clin Endocr Metab 1994; 8: 267–283.

    CAS  Google Scholar 

  111. Jameson JL. Mechanism by which thyroid hormone receptor mutations cause clinical syndromes of resistance to thyroid hormone. Thyroid 1994; 4: 485–492.

    PubMed  CAS  Google Scholar 

  112. Yen PM, Chin WW. Molecular mechanism of dominant negative activity by nuclear hormone receptors. Mol Endocrinol 1994; 8: 1450–1454.

    PubMed  CAS  Google Scholar 

  113. Wong R, Zhu XG, Pineda MA, Cheng SY, Weintraub BD. Cell type-dependent modulation of the dominant neagtive action of human mutant thyroid hormone 01 receptors. Mol Med 1995; 1: 306–319.

    PubMed  CAS  Google Scholar 

  114. Zhu XG, Yu CL, McPhie P, Wong R, Cheng SY. Understanding the molecular mechanism of dominant negative action of mutant thyroid hormone ß1-receptors: the important role of the wild-type/mutant receptor heterodimer. Endocrinology 1996; 137: 712–721.

    PubMed  CAS  Google Scholar 

  115. Nagaya T, Eberhardt N, Jameson J. Thyroid hormone resistance syndrome: correlation of dominant negative activity and location of mutations. J Clin Endocrinol Metab 1993; 77: 982–990.

    PubMed  CAS  Google Scholar 

  116. Falcone M, Miyamoto T, Fierro-Renoy F, Macchia E, DeGroot L. Antipeptide polyclonal antibodies specifically recognize each human thyroid hormone receptor isoform. Endocrinology 1992; 131: 2419–2429.

    PubMed  CAS  Google Scholar 

  117. Hayashi Y, Janssen O, Weiss RE, Murata Y, Seo H, Refetoff S. The relative expression of mutant and normal thyroid hormone receptor genes in patients with generalized resistance to thyroid hormone determined by estimation of their specific messenger ribonucleic acid products. J Clin Endocrinol Metab 1993; 76: 64–69.

    PubMed  CAS  Google Scholar 

  118. Mixson AJ, Hauser P, Tennyson G, Renault JC, Bodenner DL, Weintraub BD. Differential expression of mutant and normal beta T3 receptor alleles in kindreds with generalised resistance to thyroid hormones. J. Clin Invest 1993; 91: 2296–2300.

    PubMed  CAS  Google Scholar 

  119. Meier CA, Parkison C, Chen A, Ashizawa K, Meier-Heusler SC, Muchmore P, Cheng S-y, Weintraub BD. Interaction of human 01 thyroid hormone receptor and its mutants with DNA and retinoid X receptor. T3 response element-dependent dominant negative potency. J. Clin. Invest 1993; 92: 1986–1993.

    PubMed  CAS  Google Scholar 

  120. Zavacki AM, Harney JW, Brent GA, Larsen PR. Dominant negative inhibition by mutant thyroid hormone receptors is thyroid hormone response element and receptor isoform specific. Mol Endocrinol 1993; 7: 1319–1330.

    PubMed  CAS  Google Scholar 

  121. Weiss RE, Marcocci C, Bruno-Bossio G, Refetoff S. Multiple genetic factors in the heterogeneity of thyroid hormone resistance. J Clin Endocrinol Metab 1993; 76: 257–259.

    PubMed  CAS  Google Scholar 

  122. Forrest D, Hanebuth E, Smeyne ICI, Everds N, Stewart CL, Wehner JM, Curran T. Recessive resistance to thyroid hormone in mice lacking thyroid hormone receptor beta: evidence for tissue-specific modulation of receptor function. EMBO J 1996; 15: 3006–3015.

    CAS  Google Scholar 

  123. Forrest D, Erway LC, Ng L, Altschuler R, Curran T. Thyroid hormone receptor 13 is essential for development of auditory function. Nature Genet 1996; 13: 354–357.

    PubMed  CAS  Google Scholar 

  124. Barlow C, Meister B, Lardelli M, Lendahl U, Vennström B. Thyroid abnormalities and hepatocellular carcinoma in mice transgenic for v-erbA. EMBO J 1994; 13: 4241–4250.

    CAS  Google Scholar 

  125. Hayashi Y, Mangoura D, Refetoff S. A mouse model of resistance to thyroid hormone produced by somatic gene transfer of a mutant thyroid hormone receptor. Mol Endocrinol 1996; 10: 100–106.

    PubMed  CAS  Google Scholar 

  126. Wong R, Kutler DI, Vasilyev VV, Ting YT, Willingham M, Cheng SY, Weintraub BD. Trans-genic mice bearing human mutant thyroid hormone $1 receptor (T1431): a model of resistance to thyroid hormone (RTH) associated with fat loss and hyperactivity. Thyroid 1995;5(Supp1.1) 2:S–51(Abstract 101).

    Google Scholar 

  127. Wong GWK, Shek CC, Lam STS, Tsui MKM, Leung SSF. Detection of resistance to thyroid hormone by cord blood screening. Acta Pediatr 1995; 84: 335–336.

    CAS  Google Scholar 

  128. Beck-Peccoz P, Chatterjee VKK. The variable clinical phenotype in thyroid hormone resistance syndrome. Thyroid 1994; 4: 225–231.

    PubMed  CAS  Google Scholar 

  129. Beck-Peccoz P, Asteria C, Romoli R, Mannavola D, Cortelazzi D. In utero diagnosis of thyroid hormone resistance. J Endocrinol Invest 1996;19(Suppl. 6):72(Abstract 144).

    Google Scholar 

  130. Persani L, Asteria C, Tonacchera M, Vitti P, Chatterjee VKK, Beck-Peccoz P. Evidence for the secretion of thyrotropin with enhanced bioactivity in syndromes of thyroid hormone resistance. J Clin Endocrinol Metab 1994; 78: 1034–1039.

    PubMed  CAS  Google Scholar 

  131. Brucker-Davis F, Scarulis MC, Grace MB, Benichou J, Hauser P, Weintraub BD. Genetic and clinical features in 42 kindreds with resistance to thyroid hormone. Ann Intern Med 1995; 123: 572–583.

    PubMed  CAS  Google Scholar 

  132. Calvo R, Obregon MJ, Escobar del Rey F, Morreale de Escobar G. The rat placenta and the transfer of thyroid hormones from the mother to the fetus: effects of maternal thyroid status. Endocrinology 1992; 131: 357–363.

    PubMed  CAS  Google Scholar 

  133. Hauser P, Zametkin AJ, Martinez P, Vitiello B, Matochik JA, Mixson AJ, Weintraub BD. Attention deficit-hyperactivity disorder in people with generalised resistance to thyroid hormone. N. Engl. J. Med 1993; 328: 997–1001.

    PubMed  CAS  Google Scholar 

  134. Weiss RE, Stein M, Duck S, Chyna B, Phillips W, O’Brien T, Gutermuth L, Refetoff S. Low intelligence but not attention deficit hyperattivity disorder is associated with resistence to thyroid hormone caused by mutation R316H in the thyroid hormone receptor beta-gene. J Clin Endocr Metab 1994; 78: 1525–1528.

    PubMed  CAS  Google Scholar 

  135. Elia J, Gulotta C, Rose SR, Marin G, Rapoport J. Thyroid function and attention-deficit hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 1994; 33: 169–172.

    PubMed  CAS  Google Scholar 

  136. Spencer T, Biederman J, Wilens T, Guite J, Harding M. ADHD and thyroid abnormalities: a research note. J Child Psychol Psychiat 1995; 36: 879–885.

    PubMed  CAS  Google Scholar 

  137. Mixson AJ, Parilla R, Ransom SC, Wiggs EA, McClaskey JH, Hauser P, Weintraub BD. Correlation of language abnormalities with localization of mutations in 13 kindreds with generalised resistance to thyroid hormone: Identification of four new mutations. J Clin Endocrinol Metab 1992; 75: 1039–1045.

    PubMed  CAS  Google Scholar 

  138. Leonard CM, Martinez P, Weintraub BD, Hauser P. Magnetic resonance imaging of cerebral anomalies in subjects with resistance to thyroid hormone. Am J Med Genet 1995; 60: 238–243.

    PubMed  CAS  Google Scholar 

  139. Bradley DJ, Twole HC, Young WS. α and β thyroid hormone receptor (TR) gene expression during auditory neurogenesis: evidence for TR isoform specific transcripional regulation in vivo. Proc Natl Acad Sci USA 1994; 91: 439–443.

    PubMed  CAS  Google Scholar 

  140. Lemarchand-Béraud TH, Holm AC, Scazziga BR. Triiodothyronine and thyroxine nuclear receptors in lymphocytes from normal, hyper-and hypothyroid subjects. Acta Endocrinol (Copenh) 1977; 85: 44–54.

    Google Scholar 

  141. Ekins R. Measurement of free hormones in blood. Endocr Rev 1990; 11: 4–5.

    Google Scholar 

  142. Beck-Peccoz P, Piscitelli G, Cattaneo MG, Faglia G, White EL, Barlow JW, Stockigt JR. Evaluation of free thyroxine methods in the presence of iodiothyronine binding autoantibodies. J Clin Endocrinol Metab 1984; 58: 736–739.

    PubMed  CAS  Google Scholar 

  143. Zweig MH, Csako G, Spero M, Escape from blockade of interfering of heterophile antibodies in a two-site immunoradiometric assay for thyrotropin. Clin Chem 1988; 24: 2589–2591.

    Google Scholar 

  144. Beck-Peccoz P, Piscitelli G, Medri G, Faglia G. Thyroid test strategy (letter). Lancet 1985; i: 1456.

    Google Scholar 

  145. Papandreou M, Persani L, Asteria C, Ronin C, Beck-Peccoz P. Variable carbohydrate structure of circulating thyrotropin as studied by lectin affinity chromatography in different clinical conditions. J Clin Endocrinol Metab 1993; 77: 393–398.

    PubMed  CAS  Google Scholar 

  146. Beck-Peccoz P, Persani L. Variable biological activity of thyroid-stimulating hormone. Eur J Endocrinol 1994; 131: 331–340.

    PubMed  CAS  Google Scholar 

  147. Magee B, Sheridan B, Scanlon M, Atkins A. Inappropriate thyroitropin secretion increased dopaminergic tone and preservation of the diurnal rhytm in serum TSH. Clin Endocrinol (Oxf) 1986; 24: 209–215.

    CAS  Google Scholar 

  148. Saad B, Liu A, Brucker-Davis F, Spencer C, LoPresti J, Nicoloff J. Simplified screening for resistance to thyroid hormone (RTH)- The T3 challenge test (T3CT). Proceedings of the 77th Annual Meeting of the Endocrine Society. 1996, 211 (P1–396, Abstract).

    Google Scholar 

  149. Smallridge RC. Metabolic, physiologic, and clinical indexes of thyroid function. In: Braverman LE, Utiger RD, eds. Werner and Ingbar’s The Thyroid, 7th ed, Rowan Publishers, New York, 1996, pp. 397–405.

    Google Scholar 

  150. Faber J, Perrild H and Johansen JS. Bone Gla protein and sex hormone-binding globulin in nontoxic goiter: parameters for metabolic status at the tissue level. J Clin Endocrinol Metab 1990; 70: 49–55.

    PubMed  CAS  Google Scholar 

  151. Mariotti S, Caturegli P, Barbesino G, Marin M, Del Prete G, Chiovato L, Tonacchera M, De Carli M, Pinchera A. Thyroid function and thyroid autoimmunity independently modulate serum concentration of soluble interleukin 2 (IL-2) receptor (sIL-2R) in thyroid diseases. Clin Endocrinol (Oxf) 1992; 37: 415–422.

    CAS  Google Scholar 

  152. Harvey RD, McHardy KC, Reid IW, Paterson F, Bewsher PD, Duncan A and Robins SP. Measurement of bone collagen degradation in hyperthyroidism and during thyroxine replacement therapy using pyridinium cross-links as specific urinary markers. J Clin Endocrinol Metab 1991; 72: 1189–1194.

    PubMed  CAS  Google Scholar 

  153. Persani L, Giammona E, Cortelazzi D, Beck-Peccoz P. Carboxiterminal cross-linked telopeptide of type I collagen (ICTP) as an index of thyroid hormone effects on the bone. Proceedings of the 77th Annual Meeting of the Endocrine Society. 1995;211(P1–402, Abstract).

    Google Scholar 

  154. Same D, Refetoff S, Rosenfield R, Farriaux J. Sex hormone-binding globulin in the diagnosis of peripheral tissue resistance to thyroid hormone: the value of changes after short term triiodothyronine administration. J Clin Endocrinol Metab 1988; 66: 740–746.

    Google Scholar 

  155. Hayashi Y, Weiss RE, Same DH, Yen PM, Sunthornthepvarakul T, Marcocci C, Chin WW, Refetoff S. Do clinical manifestation of resistance to thyroid hormone correlate with the functional alteration of the corresponding mutant thyroid hormone-ß receptors? J Clin Endocrinol Metab 1995; 80: 3246–3256.

    PubMed  CAS  Google Scholar 

  156. Mixson AJ, Renault JC, Ransom S, Bodenner DL, Weintraub BD. Identification of a novel mutation in the gene encoding the ß-triiodothyronine receptor in a patient with apparent selective pituitary resistance to thyroid hormone. Clin Endocrinol (Oxf) 1993; 38: 227–234.

    CAS  Google Scholar 

  157. Beck-Peccoz P, Brucker-Davis F, Persani L, Smallridge RC, Weintraub BD. Thyrotropinsecreting pituitary tumors. Endocr Rev 1996; 17: 610–638.

    PubMed  CAS  Google Scholar 

  158. Hall WA, Luciano MG, Doppman JL, Patronas NJ, Oldfield EH. Pituitary magnetic resonance imaging in normal human volunteers: occult adenomas in the general population. Ann Intern Med 1994; 120: 817–820.

    PubMed  CAS  Google Scholar 

  159. Watanabe K, Kameya T, Yamauchi A, Yamamoto N, Kuwayama A, Takei I, Maruyama H, Saruta T. Thyrotropin-producing adenoma associated with pituitary resistance to thyroid hormone. J Clin Endocrinol Metab 1993; 76: 1025–1030.

    PubMed  CAS  Google Scholar 

  160. Beck-Peccoz P, Cortelazzi D, Persani L, Preziati D, Chatterjee VKK. Chronic treatment with vitamin A does not modify clinical and biochemical features of patients with thyroid hormone resistance. Thyroid 1994;4 (Suppl. 1) S-88 (Abstract 187).

    Google Scholar 

  161. Weiss RE, Balzano S, Scherberg NH, Refetoff S. Neonatal detection of generalized resistance to thyroid hormone. JAMA 1990; 264: 2245–2250.

    CAS  Google Scholar 

  162. Beck-Peccoz P, Cortelazzi D, Baggiani AM, Marconi AM, Buscaglia M. Evidence for trans-placental passage of 3,5,3 ’-triiodothyroacetic acid (TRIAC) in pregnant women. Thyroid 1993;(Suppl. to volume 3): T-1 (Abstract).

    Google Scholar 

  163. Sato M, Otokida K, Kato M. A case of hyperthyroidism caused by the syndrome of inappropriate secretion of thyroid-stimulating hormone: association of primary hypergonadotropic hypogonadism. Jap J Med 1989; 28: 223–227.

    CAS  Google Scholar 

  164. Dulgeroff A, Geffner M, Koyal S, Wong M, Hershman J. Bromocriptine and TRIAC therapy for hyperthyroidism due to pituitary resistance to thyroid hormone. J Clin Endocrinol Metab 1992; 75: 1071–1075.

    PubMed  CAS  Google Scholar 

  165. Schwartz ID, Bercu BB. Dextrothyroxine in the treatment of generalized thyroid hormone resistance in a boy homozygous for a defect in the T3 receptor. Thyroid 1992; 2: 15–19.

    PubMed  CAS  Google Scholar 

  166. Takeda T, Suzuki S, Liu RT, DeGroot LJ. Triiodothyroacetic acid has unique potential for therapy of resistance to thyroid hormone. J Clin Endocrinol Metab 1995; 80: 2033–2040.

    PubMed  CAS  Google Scholar 

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Beck-Peccoz, P., Asteria, C., Mannavola, D. (1997). Resistance to Thyroid Hormone. In: Braverman, L.E. (eds) Diseases of the Thyroid. Contemporary Endocrinology, vol 2. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-4757-2594-0_11

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