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28 周以下早产儿甲状腺素补充治疗后 42 个月的神经发育结局:一项随机对照试验。

Neurodevelopmental Outcomes at 42 Months After Thyroxine Supplementation in Infants Below 28 Weeks' Gestation: A Randomized Controlled Trial.

机构信息

Department of Women's and Children's Health, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.

Department of Paediatrics, Southport and Ormskirk Hospital NHS Trust, Ormskirk, United Kingdom.

出版信息

Thyroid. 2020 Jul;30(7):948-954. doi: 10.1089/thy.2019.0293. Epub 2020 Mar 17.

Abstract

Infants below 28 weeks' gestation have low thyroid hormone plasma levels compared with more mature infants and this may contribute to their risk of developmental disability. We aimed at determining the effect of supplementation with levothyroxine (LT4) for extremely premature infants born below 28 weeks' gestations on neurodevelopmental outcomes at 42 months. An explanatory double-blind, randomized, placebo-controlled trial consecutively recruited 153 infants below 28 weeks' gestation from 5 neonatal units in the United Kingdom. Infants were either supplemented with LT4 started intravenously during the first 5 days after birth and then changed to oral LT4 when enteral feeds were fully established (8 μg/kg birthweight/day as a single daily dose) or given placebo until 32 weeks' corrected gestational age. Neurodevelopmental outcomes at 42 months (range 40-43) were evaluated in 59 of these infants (30 LT4-supplemented, 29 placebo) by using Bayley III Mental and Psychomotor Developmental Indices. Cognition outcomes was correlated with plasma free thyroxine (fT4) level at 36 weeks and diffusion tensor imaging (DTI) markers. The LT4 supplemented group performed significantly better in motor, language, and cognitive function domains. The mean of the difference between each group (95% confidence intervals [CI], -value) was motor domain 6.96 ([0.55-13.38],  = 0.034); language domain 8.93 ([0.16-17.70],  = 0.041); and cognition domain 6.35 ([0.14-12.55],  = 0.045). Neurodevelopmental outcome at 42 months had some associations with the trial's primary outcome (subarachnoid space width and motor outcome,  = 0.03), plasma fT4 level at 36 weeks (fT4 and cognition outcome,  = 0.01), and DTI at 36 weeks with cognition outcomes ( > 0.05). Our data suggest that early supplementation with LT4 may improve long-term neurodevelopment in infants born below 28 weeks' gestation, but larger trials are warranted as the current reported improvements shown are not strong enough to warrant a change in practice.

摘要

早产儿胎龄小于 28 周时甲状腺激素血浆水平较低,这可能会增加其发育障碍的风险。本研究旨在确定补充左旋甲状腺素(LT4)对胎龄小于 28 周的极早产儿的影响,以评估其 42 个月时的神经发育结局。

一项解释性、双盲、随机、安慰剂对照试验连续纳入了英国 5 家新生儿单位的 153 名胎龄小于 28 周的婴儿。婴儿要么接受 LT4 补充治疗,出生后 5 天内静脉内给药,然后在完全建立肠内喂养时改为口服 LT4(8μg/kg 出生体重/天,单次剂量),要么接受安慰剂直至校正胎龄 32 周。在这些婴儿中(30 名 LT4 补充组,29 名安慰剂组),有 59 名在 42 个月时(范围 40-43 个月)进行了贝利 III 精神和运动发育指数评估。认知结局与 36 周时的游离甲状腺素(fT4)水平和弥散张量成像(DTI)标志物相关。

LT4 补充组在运动、语言和认知功能领域的表现明显更好。每组之间差异的平均值(95%置信区间[CI], 值)为运动域 6.96(0.55-13.38), = 0.034;语言域 8.93(0.16-17.70), = 0.041;认知域 6.35(0.14-12.55), = 0.045。42 个月时的神经发育结局与试验的主要结局(蛛网膜下腔宽度和运动结局, = 0.03)、36 周时的 fT4 水平(fT4 和认知结局, = 0.01)和 36 周时的 DTI 与认知结局( > 0.05)有一定关联。

我们的数据表明,早期补充 LT4 可能改善胎龄小于 28 周的早产儿的长期神经发育,但需要更大规模的试验,因为目前报告的改善程度不够强,不足以改变实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1617/7374616/63cb722a500c/thy.2019.0293_figure1.jpg

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