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轻度新生儿促甲状腺激素血症患儿3岁时甲状腺功能结局及神经预后的单中心前瞻性研究。

Single-center prospective study on thyroid function outcomes and neurological prognoses at 3 years of age in children with mild neonatal hyperthyrotropinemia.

作者信息

Sun Guoyu, Zhang Rui, Zhang Jianing, Zhou Yanxia, Tang Zezhong, Liu Lili, Hou Xinlin

机构信息

Department of Pediatrics, Peking University First Hospital, Beijing, China.

出版信息

Front Endocrinol (Lausanne). 2025 Jul 3;16:1548086. doi: 10.3389/fendo.2025.1548086. eCollection 2025.

DOI:10.3389/fendo.2025.1548086
PMID:40678318
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12267032/
Abstract

OBJECTIVE

To explore early management strategies for full-term neonates with TSH 5-10 mU/L and normal FT4.

METHODS

In this single-center longitudinal prospective study, 88 neonates diagnosed at 7-14 days were followed to age three.

RESULTS

94.3% (83/88) had transient TSH elevation; 77 normalized within two months without treatment, while six received levothyroxine (3-5µg/kg/day). Five neonates (5.7%) exhibited persistent hyperthyrotropinemia and had significantly higher initial TSH. No hyperthyroidism was observed. Following up to 3 years old, only one child (1/81, 1.2%) exhibited development delay in personal-social development. Neonates with transient hyperthyrotropinaemia scored higher in problem-solving and personal-social domains than those with persistent hyperthyrotropinaemia. Neonatal FT4 at 7-14 days, timing of TSH normalization, and maternal early-pregnancy FT4 influenced the neurodevelopment of neonates. Infants of mothers with gestational diabetes scored lower in the personal-social domain.

CONCLUSIONS

Persistent hyperthyrotropinemia occurs in 5.7% of mild cases and is associated with higher initial TSH. Levothyroxine at 3-5 µg/kg/day is both adequate and safe. The majority of neonates got a normal neurodevelopment by age 3, and the subtle difference between transient and persistent hyperthyrotropinemia was impacted by both maternal and neonatal factors.

摘要

目的

探讨促甲状腺激素(TSH)水平为5 - 10 mU/L且游离甲状腺素(FT4)正常的足月儿的早期管理策略。

方法

在这项单中心纵向前瞻性研究中,对88例在7 - 14日龄时被诊断的新生儿进行随访至3岁。

结果

94.3%(83/88)有短暂性TSH升高;77例未经治疗在两个月内TSH恢复正常,而6例接受了左甲状腺素治疗(3 - 5μg/kg/天)。5例新生儿(5.7%)表现为持续性促甲状腺激素血症,且初始TSH显著更高。未观察到甲状腺功能亢进。随访至3岁时,仅1名儿童(1/81,1.2%)在个人 - 社会发展方面出现发育迟缓。短暂性促甲状腺激素血症的新生儿在解决问题和个人 - 社会领域的得分高于持续性促甲状腺激素血症的新生儿。7 - 14日龄时的新生儿FT4、TSH恢复正常的时间以及母亲孕早期FT4影响新生儿的神经发育。患有妊娠期糖尿病母亲的婴儿在个人 - 社会领域得分较低。

结论

5.7%的轻度病例会出现持续性促甲状腺激素血症,且与更高的初始TSH相关。3 - 5μg/kg/天的左甲状腺素既足够又安全。大多数新生儿在3岁时神经发育正常,短暂性和持续性促甲状腺激素血症之间的细微差异受到母亲和新生儿因素的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1d/12267032/4d9208696076/fendo-16-1548086-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1d/12267032/f6e6e61610a7/fendo-16-1548086-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1d/12267032/a8672752069f/fendo-16-1548086-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1d/12267032/1e0368d9b807/fendo-16-1548086-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1d/12267032/4d9208696076/fendo-16-1548086-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1d/12267032/f6e6e61610a7/fendo-16-1548086-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1d/12267032/a8672752069f/fendo-16-1548086-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1d/12267032/1e0368d9b807/fendo-16-1548086-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d1d/12267032/4d9208696076/fendo-16-1548086-g004.jpg

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