Literature DB >> 15613581

Contribution of genetic factors to neonatal transient hypothyroidism.

D-M Niu1, C-Y Lin, B Hwang, T-S Jap, C-J Liao, J-Y Wu.   

Abstract

BACKGROUND: The causes of neonatal transient hypothyroidism (NTH) remain incompletely understood. Whether it is influenced by genetic background is rarely discussed and remains unproven. A defect in thyroid peroxidase is a common cause of dyshormonogenesis of the thyroid gland in Taiwanese, with a novel mutation (2268insT) present in nearly 90% of alleles studied.
OBJECTIVE: To determine if the presence of this common mutation is associated with NTH in Taiwan.
METHODS: A mismatched primer was designed and used for this specific 2268insT mutation to screen 1000 normal babies and 260 babies with confirmed NTH.
RESULTS: The carrier rate for 2268insT in normal babies (1/200) was significantly lower than in babies with NTH (1/13; p<0.0001).
CONCLUSIONS: The results strongly suggest that the presence of this thyroid peroxidase mutation contributes to the development of NTH. Likely pathogenetic explanations include the effect of the stress of extrauterine adaptation during labour on an immature pituitary-thyroid axis in genetically predisposed individuals, combined with environmental triggers such as iodine deficiency, perinatal iodine exposure, and/or goitrogen contamination.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15613581      PMCID: PMC1721821          DOI: 10.1136/adc.2003.039065

Source DB:  PubMed          Journal:  Arch Dis Child Fetal Neonatal Ed        ISSN: 1359-2998            Impact factor:   5.747


  18 in total

1.  Further evidence for a strong genetic influence on the development of autoimmune thyroid disease: the California twin study.

Authors:  Daniel A Ringold; John T Nicoloff; Matthew Kesler; Heather Davis; Ann Hamilton; Thomas Mack
Journal:  Thyroid       Date:  2002-08       Impact factor: 6.568

2.  Subclinical hypothyroidism in early childhood: a frequent outcome of transient neonatal hyperthyrotropinemia.

Authors:  Francesca Calaciura; Rosa Maria Motta; Giuseppe Miscio; Graziella Fichera; Daniela Leonardi; Anna Carta; Vincenzo Trischitta; Vittorio Tassi; Lidia Sava; Riccardo Vigneri
Journal:  J Clin Endocrinol Metab       Date:  2002-07       Impact factor: 5.958

3.  Three-year follow-up of borderline congenital hypothyroidism.

Authors:  A L Daliva; B Linder; J DiMartino-Nardi; P Saenger
Journal:  J Pediatr       Date:  2000-01       Impact factor: 4.406

4.  Transient neonatal hypothyroidism probably related to immaturity of thyroidal iodine organification.

Authors:  O Nose; T Harada; K Miyai; N Hata; M Ogawa; I Maki; S Kanaya; S Kimura; K Shimizu; H Yabuuchi
Journal:  J Pediatr       Date:  1986-04       Impact factor: 4.406

5.  Neonatal screening for congenital hypothyroidism in Europe. Report of the Newborn Committee of the European Thyroid Association.

Authors:  F Delange
Journal:  Acta Endocrinol Suppl (Copenh)       Date:  1979

6.  Neonatal thyroid function after propylthiouracil therapy for maternal Graves' disease.

Authors:  R G Cheron; M M Kaplan; P R Larsen; H A Selenkow; J F Crigler
Journal:  N Engl J Med       Date:  1981-02-26       Impact factor: 91.245

7.  Tolerance of phenylalanine after ntravenous administration in phenylketonurics, heterozygous carriers, and normal adults.

Authors:  H J Bremer; W Neumann
Journal:  Nature       Date:  1966-03-12       Impact factor: 49.962

8.  Transient hypothyroidism associated with prematurity, sepsis, and respiratory distress.

Authors:  W Schönberger; W Grimm; W Gempp; E Dinkel
Journal:  Eur J Pediatr       Date:  1979-10       Impact factor: 3.183

Review 9.  Screening for congenital hypothyroidism used as an indicator of the degree of iodine deficiency and of its control.

Authors:  F Delange
Journal:  Thyroid       Date:  1998-12       Impact factor: 6.568

10.  High prevalence of a novel mutation (2268 insT) of the thyroid peroxidase gene in Taiwanese patients with total iodide organification defect, and evidence for a founder effect.

Authors:  Dau-Ming Niu; Betau Hwang; Yum-Kung Chu; Chun-Ju Liao; Pei-Ling Wang; Ching-Yuang Lin
Journal:  J Clin Endocrinol Metab       Date:  2002-09       Impact factor: 5.958

View more
  4 in total

1.  Clinical presentation of primary congenital hypothyroidism: experience before mass screening.

Authors:  Husref Tahirović; Alma Toromanović
Journal:  Bosn J Basic Med Sci       Date:  2005-11       Impact factor: 3.363

Review 2.  Genetic causes of congenital hypothyroidism due to dyshormonogenesis.

Authors:  Helmut Grasberger; Samuel Refetoff
Journal:  Curr Opin Pediatr       Date:  2011-08       Impact factor: 2.856

3.  The role of initial clinical and laboratory findings in infants with hyperthyrotropinemia to predict transient or permanent hypothyroidism.

Authors:  Tolga Unüvar; Korcan Demir; Ayhan Abacı; Atilla Büyükgebiz; Ece Böber
Journal:  J Clin Res Pediatr Endocrinol       Date:  2013-09-10

4.  Genetic analysis in children with transient thyroid dysfunction or subclinical hypothyroidism detected on neonatal screening.

Authors:  Mari Satoh; Keiko Aso; Sayaka Ogikubo; Atsuko Ogasawara; Tsutomu Saji
Journal:  Clin Pediatr Endocrinol       Date:  2009-11-11
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.