Neonatal thyroid-stimulating hormone screening as an indirect method for the assessment of iodine deficiency in Estonia

被引:9
作者
Mikelsaar, RV
Viikmaa, M
机构
[1] Univ Tartu, Inst Gen & Mol Pathol, Dept Human Biol & Genet, EE-50411 Tartu, Estonia
[2] Univ Tartu, Inst Mol & Cell Biol, EE-50411 Tartu, Estonia
关键词
iodine deficiency; neonatal screening; congenital hypothyroidism; thyroid-stimulating hormone hyperthyrotropinemia;
D O I
10.1159/000023496
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
According to neonatal thyroid screening the incidence of congenital hypothyroidism in Estonia is 1:2,860. Transient hyperthyrotropinemia with a raised thyroid-stimulating hormone level of 5 mu U/ml occurred in 17.7% of infants and was not associated with low birth weight, small birth length, low gestational age or congenital anomalies. Based on WHO criteria (WHO/UNICEF, 1994) it corresponds to mild iodine deficiency in Estonia (3% or less is in iodine-sufficient areas). This is in agreement with the previously reported median urinary iodine content of 65 mu g/l in children. The frequency of infants with TSH >5 mu U/ml was 16.4, 21 and 17.2% in three regions (north, central and south) of Estonia, respectively, indicating mild to moderate iodine deficiency. These findings show the possibility of using the results of newborn screening for congenital hypothyroidism to assess the severity of iodine deficiency in Estonia. The introduction of universal iodine prophylaxis is recommended. Copyright (C) 2000 S. Karger AG, Basel.
引用
收藏
页码:284 / 286
页数:3
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