Increased risk of coeliac disease in patients with congenital hypothyroidism

Hormone Research in Paediatrics

Volumn 76, Issue 3, 2011, Pages 186-192

  Stagi, Stefano ^a   Manoni, Cristina ^a   Cecchi, Cecilia ^a   Chiarelli, Francesco ^b   De Martino, Maurizio ^a  

^a UNIVERSITY OF FLORENCE   (Italy)

^b UNIVERSITY OF CHIETI   (Italy)

Author keywords

Coeliac disease; Congenital hypothyroidism; Intestinal absorption; L Thyroxine

Indexed keywords

ENDOMYSIUM ANTIBODY; GLIADIN ANTIBODY; IMMUNOGLOBULIN A; PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE ANTIBODY;

ARTICLE; AUTOIMMUNE DISEASE; CELIAC DISEASE; CHILD; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; FAMILY HISTORY; FEMALE; GEOGRAPHIC DISTRIBUTION; HISTOPATHOLOGY; HUMAN; ITALY; JEJUNUM BIOPSY; MAJOR CLINICAL STUDY; MALE; PRESCHOOL CHILD; PREVALENCE; PRIORITY JOURNAL; RISK FACTOR; SCHOOL CHILD;

EID: 80054726932     PISSN: 16632818     EISSN: 16632826     Source Type: Journal    
DOI: 10.1159/000328723     Document Type: Article

References (32)

1. Toublanc JE: Comparison of epidemiological data on congenital hypothyroidism in Europe with those of other parts in the world. Horm Res 1992; 38: 230-235.
2. Park SM, Chatterjee VK: Genetics of congenital hypothyroidism. J Med Genet 2005; 42: 379-389. (Pubitemid 40685678)
3. Selva KA, Harper A, Downs A, Blasco PA, Lafranchi SH: Neurodevelopmental outcomes in congenital hypothyroidism: Comparison of initial T4 dose and time to reach target T4 and TSH. J Pediatr 2005; 147: 775-780. (Pubitemid 41774832)
4. Hrytsiuk I, Gilbert R, Logan S, Pindoria S, Brook CG: Starting dose of levothyroxine for the treatment of congenital hypothyroidism: A systematic review. Arch Pediatr Adolesc Med 2002; 156: 485-491. (Pubitemid 34492582)
5. Csako G, McGriff NJ, Rotman-Pikielny P, Sarlis NJ, Pucino F: Exaggerated levothyroxine malabsorption due to calcium carbonate supplementation in gastrointestinal disorders. Ann Pharmacother 2001; 35: 1578-1583. (Pubitemid 34027459)
6. d'Estéve-Bonetti L, Bennet AP, Malet D, Hoff M, Louvet JP, Caron P: Gluten-induced enteropathy (coeliac disease) revealed by resistance to treatment with levothyroxine and alfacalcidol in a sixty-eight-year-old patient: A case report. Thyroid 2002; 12: 633-636. (Pubitemid 34815522)
7. Barton SH, Murray JA: Celiac disease and autoimmunity in the gut and elsewhere. Gastroenterol Clin North Am 2008; 37: 411-428. (Pubitemid 351680533)
8. Salvatoni A, Maghnie M, Lorini R, Marni E: Hyponatremia and seizures during desmopressin acetate treatment in hypothyroidism. J Pediatr 1990; 116: 835-836. (Pubitemid 20162847)
9. Franzese A, Limauro R, Ecuba P, Campanile F, De Martino F, Tenore A: L-T4 malabsorption determined by intolerance to cow's milk proteins and celiac disease in a patient with congenital hypothyroidism. A clinical case. Minerva Pediatr 1993; 45: 113-116. (Pubitemid 23217638)
10. Eugster EA, LeMay D, Zerin JM, Pescovitz OH: Definitive diagnosis in children with congenital hypothyroidism. J Pediatr 2004; 144: 643-647. (Pubitemid 38594767)
11. De Vijlder JJM, Vulsma T: Hereditary metabolic disorders causing hypothyroidism; in Braverman LE, Utiger RD (eds): Werner and Ingbar's The Thyroid, ed 8. Philadelphia Lippincott Williams & Wilkins, 2000, pp 733- 742.
12. Markou KB, Paraskevopoulou P, Karaiskos KS, Makri M, Georgopoulos NA, Iconomou G, Mengreli C, Vagenakis AG: Hyperthyrotropinemia during iodide administration in normal children and in children born with neonatal transient hypothyroidism. J Clin Endocrinol Metab 2003; 88: 617-621. (Pubitemid 36207800)
13. Stagi S, Giani T, Simonini G, Falcini F: Thyroid function, autoimmune thyroiditis and coeliac disease in juvenile idiopathic arthritis. Rheumatology (Oxford) 2005; 44: 517-520. (Pubitemid 41511144)
14. Stagi S, Simonini G, Ricci L, de Martino M, Falcini F: Coeliac disease in patients with Kawasaki disease. Is there a link? Rheumatology (Oxford) 2006; 45: 847-850.
15. Cacciari E, Milani S, Balsamo A, Spada E, Bona G, Cavallo L, Cerutti F, Gargantini L, Greggio N, Tonini G, Cicognani A: Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr). J Endocrinol Invest 2006; 29: 581-593. (Pubitemid 44446267)
16. Elmlinger MW, Kühnel W, Lambrecht HG, Ranke MB: Reference intervals from birth to adulthood for serum thyroxine (T4), triiodothyronine (T3), free T3, free T4, thyroxine binding globulin (TBG) and thyrotropin (TSH). Clin Chem Lab Med 2001; 39: 973-979. (Pubitemid 33062251)
17. Oberhuber G, Granditsch G, Vogelsang H: The histopathology of coeliac disease: Time for a standardized report scheme for pathologists. Eur J Gastroenterol Hepatol 1999; 11: 1185-1194. (Pubitemid 30433773)
18. Dussault JH: Autoimmunity and congenital hypothyroidism. Arch Fr Pediatr 1987; 44(suppl 1):725-730.
19. Bona G, Chiovato L, Campra D, Paniccia P, Zaffaroni M, Costa L, Tonacchera M, Gallina MR, Giusti LF: Thyroid autoimmunity: Really an important cause of sporadic congenital hypothyroidism? Panminerva Med 1991; 33: 145-151.
20. Tsuboi K, Lima N, Ingbar SH, Medeiros-Neto G: Thyroid atrophy in myxedematous endemic cretinism: Possible role for growthblocking immunoglobulins. Autoimmunity 1991; 9: 201-206.
21. Miller LJ, Gorman CA, Go VL: Gut-thyroid interrelationships. Gastroenterology 1978; 75: 901-911. (Pubitemid 9037641)
22. Siebner R, Merlob P, Kaiserman I, Sack J: Congenital anomalies concomitant with persistent primary congenital hypothyroidism. Am J Med Genet 1992; 44: 57-60.
23. Olivieri A, Stazi MA, Mastroiacovo P, Fazzini C, Medda E, Spagnolo A, De Angelis S, Grandolfo ME, Taruscio D, Cordeddu V, Sorcini M; Study Group for Congenital Hypothyroidism: A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: Data from the Italian Registry for Congenital Hypothyroidism (1991- 1998). J Clin Endocrinol Metab 2002; 87: 557-562. (Pubitemid 34158218)
24. Chao T, Wang JR, Hwang B: Congenital hypothyroidism and concomitant anomalies. J Pediatr Endocrinol Metab 1997; 10: 217-221. (Pubitemid 27223670)
25. Stoll C, Dott B, Alembik Y, Koehl C: Congenital anomalies associated with congenital hypothyroidism. Ann Genet 1999; 42: 17-20. (Pubitemid 29145817)
26. Berant M, Diamond E, Mabriki W, Ben-Yitzhak O: Effects of hypothyroidism on jejunal mucosal function: Study by in situ luminal perfusion in rats. Pediatr Res 1993; 34: 79-83. (Pubitemid 23177765)
27. Van Vliet G: Development of the thyroid gland: Lessons from congenitally hypothyroid mice and men. Clin Genet 2003; 63: 445-455. (Pubitemid 36944090)
28. Castanet M, Polak M, Bonaïti-Pellié C, Lyonnet S, Czernichow P, Léger J; AFDPHE (Association Française pour le Dépistage et la Prévention des Handicaps de l'Enfant): Nineteen years of national screening for congenital hypothyroidism: Familial cases with thyroid dysgenesis suggest the involvement of genetic factors. J Clin Endocrinol Metab 2001; 86: 2009-2014. (Pubitemid 32472912)
29. Caputo M, Brizzolara R, Schiavo M, Salmaso C, Pesce G, Bagnasco M: Occurrence of overt celiac disease in the elderly following total thyroidectomy. J Endocrinol Invest 2006; 29: 831-833. (Pubitemid 44869429)
30. Certo M, Mancini A, Fiumara C, Conte G, Valle D, Abagnale R, Rabitti C, De Marinis L: Gastroenterologic pathology and replacement organotherapy in thyroidectomized patients (in Italian). Minerva Chir 1993; 48: 1319-1323.
31. Harzallah F, Daoud I, Bouzid C, Oueslati A, Kanoun F, Slimane H: Celiac disease revealed by hypocalcemia complicating total thyroidectomy: A case report. Ann Endocrinol (Paris) 2006; 67: 357-359.
32. Collin P, Salmi J, Hällström O, Reunala T, Pasternack A: Autoimmune thyroid disorders and coeliac disease. Eur J Endocrinol 1994; 130: 137-140. (Pubitemid 24112382)