Department of Endocrinology, Great Ormond Street Hospital for Children, London, UK.
University of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
Eur J Endocrinol. 2022 Jun 20;187(2):R1-R16. doi: 10.1530/EJE-21-1278.
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.
一过性先天性甲状腺功能减退症(TCH)是指在生命最初几个月或几年内自行缓解的先天性甲状腺功能减退症。目前,在诊断时缺乏可靠的预测 TCH 的标志物,并且在大约 3 岁时停止左旋甲状腺素治疗后才做出诊断。TCH 的发病率正在增加,它是近年来 CH 总体发病率增加的主要原因之一。遗传因素,特别是影响 DUOX2 和 DUOXA2 的突变,以及环境因素,如碘缺乏和过量、抗 TSHR 抗体和接触抗甲状腺或富含碘的药物,都可能导致 TCH。儿童时期 TCH 的缓解可能反映了正常的甲状腺生理(新生儿期后甲状腺激素生物合成需求减少)以及环境诱因的清除或停止。遗传和环境因素对 TCH 的相对贡献和相互作用,以及 TCH 可能预防的程度,需要在未来的基于人群的研究中进行评估。