MECHANISMS IN ENDOCRINOLOGY The pathophysiology of transient congenital hypothyroidism

被引:20
作者
Peters, Catherine [1 ]
Schoenmakers, Nadia [2 ]
机构
[1] Great Ormond St Hosp Sick Children, Dept Endocrinol, London, England
[2] Univ Cambridge, MRC Inst Metab Sci, Wellcome Trust, Metab Res Labs, Cambridge, England
基金
英国惠康基金;
关键词
THYROID-STIMULATING HORMONE; RECEPTOR-BLOCKING ANTIBODIES; IODINATED CONTRAST-MEDIA; PREGNANT-WOMEN; CONSUMPTIVE HYPOTHYROIDISM; SCREENING-PROGRAM; PREMATURE-INFANTS; MACRO-THYROTROPIN; DUOX2; MUTATIONS; UNITED-STATES;
D O I
10.1530/EJE-21-1278
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Transient congenital hypothyroidism (TCH) refers to congenital hypothyroidism which spontaneously resolves in the first few months or years of life. Currently, there is a paucity of reliable markers predicting TCH at diagnosis, and the diagnosis is established following the withdrawal of levothyroxine therapy around 3 years of age. The incidence of TCH is increasing, and it is a major contributor to the overall increase in the incidence of CH in recent studies. Both genetic factors, in particular mutations affecting DUOX2 and DUOXA2, and environmental factors, for example, iodine deficiency and excess, anti-TSHR antibodies and exposure to antithyroid or iodine-rich medications, may cause TCH. Resolution of TCH in childhood may reflect both normal thyroid physiology (decreased thyroid hormone biosynthesis requirements after the neonatal period) and clearance or cessation of environmental precipitants. The relative contributions and interactions of genetic and environmental factors to TCH, and the extent to which TCH may be prevented, require evaluation in future population-based studies.
引用
收藏
页码:R1 / R16
页数:16
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