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A study of the etiology of transient congenital hypothyroidism in Niigata Prefecture, Japan

  • Keisuke Nagasaki
  • Satoshi Narumi
  • Kiyomi Abe
  • Tadashi Asami
  • Hidetoshi Sato
  • Yohei Ogawa
  • Toru Kikuchi
  • Tomonobu Hasegawa
  • Akihiko Saitoh
Open Access
Oral presentation

Keywords

Iodine Iodine Deficiency Iodine Concentration Congenital Hypothyroidism Propylthiouracil 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Background

Several conditions have been known to causetransient congenital hypothyroidism (TCH), including transplacental passage of TSH receptor blocking antibody (TSBAb), maternal antithyroid drug usage, iodine deficiency, iodine excess, fetal prematurity and inactivatingDUOX2 mutations. However, the underlying etiology of TCH is not determined in some cases. In this study, we conducted the first systematic investigation on the etiology of TCH, using screening population-based cohort in Niigata Prefecture, Japan.

Methods

Between April 2003 and March 2009, 148,100 newborns were screened for CH in Niigata prefecture, and 159 patients were considered positive for CH. We diagnosed patients as having TCH that fulfilled the following two criteria: 1) serum TSH level >30 mU/L and serum FT4 level <1.5 ng/dLat the initial examination, 2) serum TSH level <5 mU/L while investigative discontinuation of thyroxine replacement at 2 years of age. A total of 9 patients (1/16,500) diagnosed with TCH were evaluated. To determine the etiology of TCH, we examined the following: 1) maternal medical history, 2)gestational age and birth weight, 3) maternal anti-thyroid antibodies, 4) urinary iodine concentration at initial visit, and 5) DNA sequence of DUOX2.

Results

Among the nine TCH patients, one had extremely high maternal TSBAb level, one was exposed to propylthiouracil, and two were exposed to excessive iodine.Furthermore, we found that five had biallelicDUOX2 mutations.

Conclusions

DUOX2 mutations were the majorcause of TCH in our cohort study.

Copyright information

© Nagasaki et al; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Authors and Affiliations

  • Keisuke Nagasaki
    • 1
  • Satoshi Narumi
    • 2
  • Kiyomi Abe
    • 2
  • Tadashi Asami
    • 3
  • Hidetoshi Sato
    • 1
  • Yohei Ogawa
    • 1
  • Toru Kikuchi
    • 1
  • Tomonobu Hasegawa
    • 2
  • Akihiko Saitoh
    • 1
  1. 1.Division of Pediatrics, Department of Homeostatic Regulation and DevelopmentNiigata University Graduate School of Medical andDental SciencesNiigataJapan
  2. 2.Department of PediatricsKeio University School of MedicineTokyoJapan
  3. 3.Department of Nursing, Faculty of Nursing, Social Welfare, and PsychologyNiigata Seiryo UniversityNiigataJapan

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