Boelen Anita, Heijboer Annemieke C
Eur Thyroid J. 2025 Feb 10;14(1). doi: 10.1530/ETJ-24-0325. Print 2025 Feb 1.
Thyroid hormone (TH) is essential for brain development in utero and during the first 2 to 3 years of life. The negative effects of TH deficiency on brain development are irreversible. Early detection of TH deficiency in neonates (congenital hypothyroidism (CH) through newborn screening (NBS)) allows for early treatment, thereby preventing brain damage. Screening for CH began in 1973 with the measurement of total thyroxine (T4) in dried blood spots. The enhanced sensitivity of thyroid-stimulating hormone (TSH) measurement has prompted a shift in the approach to NBS for CH. Currently, worldwide, the majority of NBS programs for CH employ TSH as the primary screening marker. However, a select few programs still utilize T4 as the primary marker, enabling the detection of both primary and central CH. This review provides an overview of the laboratory aspects of the screening on CH from the start of screening to the present.
甲状腺激素(TH)对于胎儿期及生命最初2至3年的大脑发育至关重要。TH缺乏对大脑发育的负面影响是不可逆的。通过新生儿筛查(NBS)早期发现新生儿甲状腺激素缺乏(先天性甲状腺功能减退症(CH))可实现早期治疗,从而预防脑损伤。CH筛查始于1973年,当时通过检测干血斑中的总甲状腺素(T4)进行。促甲状腺激素(TSH)检测灵敏度的提高促使CH的NBS方法发生了转变。目前,在全球范围内,大多数CH的NBS项目都将TSH作为主要筛查标志物。然而,仍有少数项目仍将T4作为主要标志物,从而能够检测原发性和中枢性CH。本综述概述了从筛查开始至今CH筛查的实验室相关情况。