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儿童自身免疫性甲状腺炎所致严重甲状腺功能减退症的临床和生化特征。

Clinical and Biochemical Characteristics of Severe Hypothyroidism Due to Autoimmune Thyroiditis in Children.

机构信息

Department of Paediatrics and Endocrinology, Medical University of Warsaw, Warsaw, Poland.

出版信息

Front Endocrinol (Lausanne). 2020 Jul 8;11:364. doi: 10.3389/fendo.2020.00364. eCollection 2020.

Abstract

In the majority of countries, autoimmune thyroiditis is the main cause of acquired hypothyroidism in children. Typically, the natural course of the disease is initially insidious and the diagnosis is incidental. There are some children who develop severe hypothyroidism without a proper diagnosis. The aim of the study was to analyze the clinical and biochemical profiles of children with severe primary hypothyroidism due to autoimmune thyroiditis. We analyzed the records of 354 patients diagnosed between 2009 and 2019 with autoimmune thyroiditis. Only patients with TSH above 100 μIU/mL, associated with decreased free thyroxine and the presence of antithyroid antibodies, were enrolled in the study. The analysis encompassed clinical symptoms, thyroid and biochemical status, bone age, and imaging. Twenty-six children were enrolled in the study. The mean age at diagnosis was 10.26 ± 3.3 years, with a female preponderance of 1.8:1. The most frequent symptom was growth impairment (77%) and weight gain (58%). Goiters were present in 42% of patients. Less common findings were pituitary hypertrophy (four patients) and hypertrichosis (three patients). Median values at the time of diagnosis were TSH 454.3 uIU/ml (295.0-879.4), anti-TPO antibodies 1,090 IU/ml, and anti-Tg antibodies 195 IU/ml. Anti-TSHR ab were evaluated only in six out of the 26 patients. The characteristic biochemical profile was correlated with the grade of hypothyroidism, and the strongest correlations were found with CBC parameters, lipid profile, aminotransferases, and creatine. In children with severe hypothyroidism, the most sensitive symptoms are growth arrest and weight gain despite the fact that, in some children, the auxological parameters at presentation could be within normal values for the population. The specific biochemical profile closely correlates to the severity of thyroid hormone deficiency and involves mostly erythropoiesis, liver function, and kidney function. Pituitary enlargement should be considered in each child with severe hypothyroidism. It is necessary to conduct prospective studies evaluating the actual frequency of anti-TSHR antibodies and pituitary enlargement in children with extremely high TSH, especially those presenting without goiters.

摘要

在大多数国家,自身免疫性甲状腺炎是儿童获得性甲状腺功能减退症的主要原因。通常,疾病的自然病程起初隐匿,诊断为偶发。有些儿童会发展为严重的甲状腺功能减退症,而没有得到适当的诊断。本研究旨在分析自身免疫性甲状腺炎引起的严重原发性甲状腺功能减退症患儿的临床和生化特征。

我们分析了 2009 年至 2019 年间诊断为自身免疫性甲状腺炎的 354 名患者的记录。仅纳入 TSH 高于 100 μIU/ml、游离甲状腺素降低且存在抗甲状腺抗体的患者进行研究。分析内容包括临床症状、甲状腺和生化状态、骨龄和影像学检查。

本研究纳入了 26 名患儿。诊断时的平均年龄为 10.26 ± 3.3 岁,女性占比为 1.8:1。最常见的症状是生长发育迟缓(77%)和体重增加(58%)。42%的患者存在甲状腺肿。较少见的发现包括垂体肥大(4 例)和多毛症(3 例)。诊断时的中位值为 TSH 454.3 uIU/ml(295.0-879.4)、抗甲状腺过氧化物酶抗体 1090 IU/ml 和抗甲状腺球蛋白抗体 195 IU/ml。仅对 26 名患儿中的 6 名进行了抗促甲状腺激素受体抗体检测。特征性生化特征与甲状腺功能减退的严重程度相关,与 CBC 参数、血脂谱、氨基转移酶和肌酸密切相关。

在严重甲状腺功能减退的儿童中,最敏感的症状是生长停滞和体重增加,尽管在一些儿童中,就诊时的生长参数可能在人群正常值范围内。特定的生化特征与甲状腺激素缺乏的严重程度密切相关,主要涉及红细胞生成、肝功能和肾功能。对于每个患有严重甲状腺功能减退症的儿童,都应考虑是否存在垂体增大。有必要开展前瞻性研究,评估 TSH 极高的儿童,尤其是那些没有甲状腺肿的儿童,其抗促甲状腺激素受体抗体和垂体增大的实际发生率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f408/7360718/a4f96ad1562a/fendo-11-00364-g0001.jpg

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