• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

新生儿先天性甲状腺功能减退症筛查:巴西米纳斯吉拉斯州28年的经验。

Neonatal screening for congenital hypothyroidism: 28-year experience in the state of Minas Gerais, Brazil.

作者信息

Braga Nathalia Teixeira Palla, Alves Debora Patrícia da Silva Sousa, Colosimo Enrico Antônio, Dias Vera Maria Alves, Januário José Nélio, Silva Ivani Novato

机构信息

Pediatric Endocrinology Service, Hospital das Clínicas, Universidade Federal de Minas Gerais, Brazil.

Pediatric Endocrinology Service, Hospital das Clínicas, Universidade Federal de Minas Gerais, Brazil.

出版信息

J Pediatr (Rio J). 2025 May-Jun;101(3):430-437. doi: 10.1016/j.jped.2024.12.007. Epub 2025 Mar 18.

DOI:10.1016/j.jped.2024.12.007
PMID:40037552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12039367/
Abstract

OBJECTIVE

The objective of this study was to determine the incidence of congenital hypothyroidism (CH) in Minas Gerais, Brazil, and evaluate the development of the Minas Gerais Neonatal Screening Program (PTN-MG) over the past 30 years.

METHOD

This was a retrospective longitudinal cohort study since the implementation of neonatal screening for CH, in 1994. Bloodspots on filter paper are collected, between the third and fifth day of life, at primary healthcare units, with a TSH threshold of 10 mIU/L. The identification of an abnormal result triggers an active search for the child to confirm the diagnosis. The incidence of CH and its variation over the years, the percentage of permanent cases, and the age at sample collection and treatment initiation were analyzed.

RESULTS

The incidence of CH was 1:3,298 live births among 6,864,719 newborns screened, with no trend of change over the years (p = 0.08). The median age at sample collection decreased from 11 to 5 days (p < 0.01) and at treatment initiation from 88 to 16 days (p < 0.01). Among the confirmed patients, 77 % had permanent CH, thyroid dysgenesis accounted for 43.6 % of cases, gland-in-situ for 56.3 %.

CONCLUSION

The incidence of CH has remained stable in Minas Gerais over the past 28 years. The PTN-MG is a public health program with an active monitoring and control sector that has shown significant improvements in its indicators since its implementation. The experience of the program has shown that rigorous monitoring and follow-up of infants have been an essential strategy for achieving satisfactory results.

摘要

目的

本研究的目的是确定巴西米纳斯吉拉斯州先天性甲状腺功能减退症(CH)的发病率,并评估米纳斯吉拉斯州新生儿筛查项目(PTN-MG)在过去30年中的发展情况。

方法

这是一项回顾性纵向队列研究,自1994年实施CH新生儿筛查以来。在生命的第三天至第五天,在基层医疗单位采集滤纸血斑,促甲状腺激素(TSH)阈值为10 mIU/L。异常结果的识别会促使积极寻找患儿以确诊。分析了CH的发病率及其多年来的变化、永久性病例的百分比以及样本采集和开始治疗的年龄。

结果

在6,864,719名接受筛查的新生儿中,CH的发病率为1:3,298活产,多年来无变化趋势(p = 0.08)。样本采集的中位年龄从11天降至5天(p < 0.01),开始治疗的中位年龄从88天降至16天(p < 0.01)。在确诊患者中,77%患有永久性CH,甲状腺发育不全占病例的43.6%,甲状腺原位占56.3%。

结论

在过去28年中,米纳斯吉拉斯州CH的发病率一直保持稳定。PTN-MG是一个拥有积极监测和控制部门的公共卫生项目,自实施以来其指标有显著改善。该项目的经验表明,对婴儿进行严格的监测和随访是取得满意结果的关键策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c71/12039367/521a814ef02a/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c71/12039367/b1de413891ff/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c71/12039367/215b5e68714e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c71/12039367/a8e11e55eccf/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c71/12039367/521a814ef02a/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c71/12039367/b1de413891ff/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c71/12039367/215b5e68714e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c71/12039367/a8e11e55eccf/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c71/12039367/521a814ef02a/gr4.jpg

相似文献

1
Neonatal screening for congenital hypothyroidism: 28-year experience in the state of Minas Gerais, Brazil.新生儿先天性甲状腺功能减退症筛查:巴西米纳斯吉拉斯州28年的经验。
J Pediatr (Rio J). 2025 May-Jun;101(3):430-437. doi: 10.1016/j.jped.2024.12.007. Epub 2025 Mar 18.
2
Incidence of congenital hypothyroidism in the city of Uberaba/Minas Gerais and etiological evaluation of the affected subjects.乌贝拉巴市/米纳斯吉拉斯州先天性甲状腺功能减退症的发病率及患病者的病因学评估。
Arq Bras Endocrinol Metabol. 2012 Jul;56(5):305-12. doi: 10.1590/s0004-27302012000500005.
3
Screening for congenital hypothyroidism in extreme premature and/or very low birth weight newborns: the importance of a specific protocol.极低出生体重儿和/或超早产儿先天性甲状腺功能减退症的筛查:特定方案的重要性
J Pediatr Endocrinol Metab. 2010 Jan-Feb;23(1-2):45-52. doi: 10.1515/jpem.2010.23.1-2.45.
4
A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH).一项针对新生儿筛查采用低促甲状腺激素(TSH)临界值水平的7年经验显示,先天性甲状腺功能减退症(CH)的发生率出人意料。
Clin Endocrinol (Oxf). 2009 Nov;71(5):739-45. doi: 10.1111/j.1365-2265.2009.03568.x. Epub 2009 Mar 28.
5
The etiologies and incidences of congenital hypothyroidism before and after neonatal TSH screening program implementation: a study in southern Thailand.新生儿促甲状腺激素筛查项目实施前后先天性甲状腺功能减退症的病因及发病率:泰国南部的一项研究
J Pediatr Endocrinol Metab. 2018 Jun 27;31(6):609-617. doi: 10.1515/jpem-2017-0340.
6
Changes in the incidence and etiology of congenital hypothyroidism detected during 30 years of a screening program in central Serbia.塞尔维亚中部一项筛查计划30年间先天性甲状腺功能减退症的发病率及病因变化。
Eur J Pediatr. 2016 Feb;175(2):253-9. doi: 10.1007/s00431-015-2630-5. Epub 2015 Sep 7.
7
Primary Congenital Hypothyroidism in Children Below 3 Years Old - Etiology and Treatment With Overtreatment and Undertreatment Risks, a 5-Year Single Centre Experience.3 岁以下儿童原发性先天性甲状腺功能减退症-有过度治疗和治疗不足风险的病因和治疗,5 年单中心经验。
Front Endocrinol (Lausanne). 2022 Jun 27;13:895507. doi: 10.3389/fendo.2022.895507. eCollection 2022.
8
Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidism.先天性甲状腺功能减退症由于甲状腺发育缺陷和筛查时 TSH 轻度升高:来自意大利先天性甲状腺功能减退症婴儿国家登记处的数据。
J Clin Endocrinol Metab. 2013 Apr;98(4):1403-8. doi: 10.1210/jc.2012-3273. Epub 2013 Feb 26.
9
Newborn Screening for Congenital Hypothyroidism: the Benefit of Using Differential TSH Cutoffs in a 2-Screen Program.新生儿先天性甲状腺功能减退症筛查:在双筛查程序中使用差异化 TSH 切点的益处。
J Clin Endocrinol Metab. 2021 Jan 1;106(1):e338-e349. doi: 10.1210/clinem/dgaa789.
10
Evolution to permanent or transient conditions in children with positive neonatal TSH screening tests in Sergipe, Brazil.巴西塞尔希培州新生儿促甲状腺激素筛查试验呈阳性的儿童发展为永久性或暂时性病症的情况。
Arch Endocrinol Metab. 2016 Oct;60(5):450-456. doi: 10.1590/2359-3997000000189. Epub 2016 Aug 25.

本文引用的文献

1
The newborn screening tests in Brazil: regional and socioeconomic prevalence and inequalities in 2013 and 2019.巴西的新生儿筛查测试:2013年和2019年的区域及社会经济患病率与不平等情况
J Pediatr (Rio J). 2024 May-Jun;100(3):296-304. doi: 10.1016/j.jped.2023.11.008. Epub 2023 Dec 31.
2
Epidemiological profile of congenital hypothyroidism at a southern Brazilian state.巴西南部一州先天性甲状腺功能减退症的流行病学特征。
Arch Endocrinol Metab. 2023 May 12;67(4):e000606. doi: 10.20945/2359-3997000000606.
3
Outcomes of lowered newborn screening thresholds for congenital hypothyroidism.
降低先天性甲状腺功能减退症新生儿筛查阈值的结果。
J Paediatr Child Health. 2023 Aug;59(8):955-961. doi: 10.1111/jpc.16425. Epub 2023 May 15.
4
Incidence of primary congenital hypothyroidism over 24 years in Finland.芬兰 24 年原发性先天性甲状腺功能减退症的发病率。
Pediatr Res. 2023 Feb;93(3):649-653. doi: 10.1038/s41390-022-02118-4. Epub 2022 Jun 3.
5
Transient vs Permanent Congenital Hypothyroidism in Ontario, Canada: Predictive Factors and Scoring System.加拿大安大略省的暂时性与永久性先天性甲状腺功能减退症:预测因素和评分系统。
J Clin Endocrinol Metab. 2022 Feb 17;107(3):638-648. doi: 10.1210/clinem/dgab798.
6
Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010.欧洲新生儿筛查再审视:国际新生儿筛查学会对2010年以来现状与发展的观点
Int J Neonatal Screen. 2021 Mar 5;7(1):15. doi: 10.3390/ijns7010015.
7
Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology.先天性甲状腺功能减退症:2020-2021 年共识指南更新——一项由 ENDO-欧洲参考网络倡议发起并得到欧洲儿科内分泌学会和欧洲内分泌学会认可的倡议。
Thyroid. 2021 Mar;31(3):387-419. doi: 10.1089/thy.2020.0333.
8
Impact of the reduction in TSH cutoff level to 6 mIU/L in neonatal screening for congenital hypothyroidism in Santa Catarina: final results.降低新生儿先天性甲状腺功能减退症筛查中 TSH 截断值至 6 mIU/L 对圣卡塔琳娜州的影响:最终结果。
Arch Endocrinol Metab. 2021 Nov 1;64(6):816-823. doi: 10.20945/2359-3997000000299. Epub 2020 Oct 21.
9
The impact of demographic factors on newborn TSH levels and congenital hypothyroidism screening.人口统计学因素对新生儿 TSH 水平和先天性甲状腺功能减退症筛查的影响。
Clin Endocrinol (Oxf). 2019 Sep;91(3):456-463. doi: 10.1111/cen.14044. Epub 2019 Jun 11.
10
Incidence of Congenital Hypothyroidism Over 37 Years in Ireland.爱尔兰 37 年来先天性甲状腺功能减退症的发病率。
Pediatrics. 2018 Oct;142(4). doi: 10.1542/peds.2018-1199.