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早产儿的甲状腺功能与 2 岁时的神经发育。

Thyroid function in preterm infants and neurodevelopment at 2 years.

机构信息

Division of Population Health & Genomics, School of Medicine, University of Dundee, Dundee, UK

Medical Student, Medical School, Ninewells Hospital and Medical School, Dundee, UK.

出版信息

Arch Dis Child Fetal Neonatal Ed. 2020 Sep;105(5):504-509. doi: 10.1136/archdischild-2018-316742. Epub 2020 Feb 20.

Abstract

OBJECTIVES

Postnatal thyroid dysfunction is common in preterm infants but the relationship between mild dysfunction and neurodevelopment is unclear. Our aim is to describe the relationship between thyroid function and neurodevelopment.

DESIGN

Cohort analysis.

PATIENTS

1275 infants born under 31 weeks' gestation; there were no exclusion criteria.

SETTING

The infants were part of a UK daily iodine supplementation trial.

MAIN OUTCOMES

Thyroid-stimulating hormone, thyroid-binding globulin and total thyroxine levels were measured in dried blood spots on postnatal days 7, 14, 28 and the equivalent of 34 weeks' gestation. Neurodevelopment was measured using the Bayley-III Scales of infant development at 2 years of age.

RESULTS

No infant was identified as hypothyroid through routine screening. The 3% of infants consistently in the top decile of gestationally age-adjusted thyroid-stimulating hormone levels had a reduction in cognitive score of 7 Bayley units when compared with those not in the top decile (95% CI -13 to -1). A reduction in motor composite score of 6 units (95% CI -12 to <-0.1) and fine motor score of 1 unit (95% CI -2 to -0.1) was also identified. The 0.7% of infants consistently in the bottom decile of age-adjusted thyroxine levels had a reduction in motor composite score of 14 units (95% CI -25 to -2) and its two subset scores, fine and gross motor, of 2 units (95% CI respectively -4.5 to <-0.1 and -4.3 to -0.3).

CONCLUSIONS

Preterm infants with consistent 'mild' thyroid dysfunction score less on neurodevelopmental tests at 2 years of age. Many of these infants will not be detected by current clinical protocols or screening programmes.

摘要

目的

早产儿产后甲状腺功能障碍很常见,但轻度功能障碍与神经发育之间的关系尚不清楚。我们旨在描述甲状腺功能与神经发育之间的关系。

设计

队列分析。

患者

1275 名胎龄小于 31 周的婴儿;无排除标准。

设置

这些婴儿是英国每日补充碘试验的一部分。

主要结果

在出生后第 7、14、28 天和相当于 34 周胎龄时,通过干血斑测量促甲状腺激素、甲状腺结合球蛋白和总甲状腺素水平。在 2 岁时使用贝利婴幼儿发育量表测量神经发育。

结果

没有婴儿通过常规筛查被确定为甲状腺功能减退。3%的婴儿持续处于促甲状腺激素水平与胎龄相适应的最高十分位数,其认知评分比不在最高十分位数的婴儿低 7 个贝利单位(95%CI-13 至-1)。运动综合评分降低 6 个单位(95%CI-12 至-0.1),精细运动评分降低 1 个单位(95%CI-2 至-0.1)。0.7%的婴儿持续处于与年龄相适应的甲状腺素水平的最低十分位数,其运动综合评分降低 14 个单位(95%CI-25 至-2),其两个亚组评分,精细运动和粗大运动评分,降低 2 个单位(95%CI 分别为-4.5 至<-0.1 和-4.3 至-0.3)。

结论

持续性“轻度”甲状腺功能障碍的早产儿在 2 岁时神经发育测试得分较低。许多这样的婴儿不会被现行的临床方案或筛查计划检测到。

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