先天性甲状腺功能减退:目前的观点

D. Dayal, R. Prasad
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引用次数: 19

摘要

先天性甲状腺功能减退症(CH)是最常见的儿科内分泌疾病,估计患病率为1:20 00至1:4 000,在没有常规新生儿筛查(NBS)计划的国家,这是一个未得到充分认识的问题。甲状腺发育不良(TD)是原发性CH最常见的原因,约占所有病例的85%;其余大多数患者都有激素生成障碍。在引入常规NBS后,越来越多地发现瞬态CH和异位腺体CH。CH的临床特征往往很微妙,导致诊断延迟,最终导致智力低下。在发达国家,国家统计局的检测和早期治疗已经在很大程度上消除了由这种疾病引起的智力障碍。在一些国家,较低的促甲状腺激素(TSH)筛查截止值和出生人口统计数据的变化与报告的CH发病率增加有关。然而,较低的促甲状腺激素截止值检测到的额外病例往往是轻度或短暂性甲状腺功能减退。诊断CH是根据血清TSH和甲状腺素(T4)的浓度。甲状腺超声、放射性核素显像、血清甲状腺球蛋白(TG)水平和特异性基因检测有助于确定确切的病因诊断。不能获得后来的测试不应该阻止儿科医生开始治疗。开始治疗的年龄和左旋甲状腺素的起始剂量是决定长期预后的关键因素。婴儿需要更高剂量的左甲状腺素,剂量为10-15 μg/kg/天,根据T4和TSH水平进行滴定,并经常重复。CH患儿同时存在其他先天性异常,增加了发病率。全世界约70%的婴儿并非出生在已建立国家卫生系统规划的地区,因此没有及早发现和治疗。因此,在没有国家统计局的国家中,由CH引起的智力迟钝的经济负担仍然是一个重大的公共卫生挑战。即使在国家统计局十分发达的国家,由卫生保健造成的卫生负担仍然很高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital hypothyroidism: current perspectives
Congenital hypothyroidism (CH), the most common pediatric endocrine disorder with an estimated prevalence of 1:2,000 to 1:4,000, is an under-recognized problem in countries without routine newborn screening (NBS) programs. Thyroid dysgenesis (TD) is the most com- mon cause of primary CH accounting for approximately 85% of all cases; most of the remaining patients have dyshormonogenesis. Transient CH and CH with eutopic gland, are increasingly being identified after introduction of routine NBS. The clinical features of CH are often subtle resulting in delayed diagnosis and eventually poor intellectual outcome. In developed countries, detection by NBS and early initiation of treatment has largely eliminated the intellectual dis- ability caused by this disorder. The lower screening thyroid stimulating hormone (TSH) cutoff and changes in birth demographics in some countries have been associated with an increase in the reported incidence of CH. However, the additional cases detected by the lower TSH cutoff tend to have either milder or transient hypothyroidism. Diagnosis of CH is made on the basis of serum concentrations of TSH and thyroxine (T4). Thyroid ultrasound, radionuclide scintigraphy, serum thyroglobulin (TG) levels and specific genetic tests help ascertaining the exact etiological diagnosis. Non-availability of later tests should not deter the pediatrician from initiation of treat- ment. Age at initiation of treatment and starting dose of levothyroxine are critical factors that determine the long-term outcome. Higher doses of levothyroxine at 10-15 μg/kg/day are required in infants, with titration based on T4 and TSH levels, which are repeated frequently. Coexistence of other congenital anomalies in children with CH adds to the morbidity. Approximately 70% of babies worldwide are not born in an area with an established NBS program and hence are not detected and treated early. Consequently, the economic burden of mental retardation due to CH remains a significant public health challenge in countries without NBS. The health burden owing to CH continues to be high even in countries with well-developed NBS.
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