Williams Fiona L R, Ogston Simon A, van Toor Hans, Visser Theo J, Hume Robert
Community Health Sciences, University of Dundee, Ninewells Hospital and Medical School, Dundee DD1 9SY, Scotland, United Kingdom.
J Clin Endocrinol Metab. 2005 Nov;90(11):5954-63. doi: 10.1210/jc.2005-1049. Epub 2005 Aug 16.
Transient hypothyroxinemia is common in infants less than 30 wk gestation and is associated with neurodevelopmental deficits. Reductions in T4 and T3 levels with TSH unchanged are the key features of severe illness using surrogate indices of overall severity of illness, but these do not inform the impact of individual disease conditions or drug use.
Our objective was to investigate the contribution of postnatal factors to the variations in serum levels of iodothyronines, thyroid-binding globulin, and TSH.
We recruited a cohort of infants (23-34 wk gestation; n = 780) between January 1998 and September 2001.
The study involved 11 level III Scottish neonatal intensive care units and included cohorts of infants delivered at 23-34 wk gestation.
We assessed serum levels of iodothyronines, thyroid-binding globulin, and TSH at 7, 14, and 28 d adjusted for the potentially significant postnatal influences (n = 31).
Serum levels of TSH, free T4, T3, and T4 are variably but significantly associated with bacteremia, endotracheal bacterial cultures, persistent ductus arteriosus, necrotizing enterocolitis, cerebral ultrasonography changes, oxygen dependence at 28 d, and the use of aminophylline, caffeine, dexamethasone, diamorphine, and dopamine.
There are many more associations of postnatal factors with transient hypothyroxinemia than had previously been considered in preterm infants. Alternative strategies should be considered for correction of hypothyroxinemia rather than sole reliance on the direct therapy of hormone replacement. A more oblique preventative approach may be necessary through reduction in the incidence or severity of individual illness(es). Similarly, alternatives to those drugs that interfere with the hypothalamic-pituitary-thyroid axis should be evaluated (e.g. other inotropics instead of dopamine).
短暂性甲状腺素血症在孕周小于30周的婴儿中很常见,且与神经发育缺陷有关。使用疾病总体严重程度的替代指标时,T4和T3水平降低而TSH不变是重症疾病的关键特征,但这些指标无法说明个体疾病状况或药物使用的影响。
我们的目的是研究出生后因素对血清甲状腺素、甲状腺结合球蛋白和TSH水平变化的影响。
我们在1998年1月至2001年9月期间招募了一组婴儿(孕周23 - 34周;n = 780)。
该研究涉及11个苏格兰三级新生儿重症监护病房,纳入了孕周为23 - 34周的婴儿队列。
我们在调整了潜在的显著出生后影响因素后(n = 31),于第7、14和28天评估了血清甲状腺素、甲状腺结合球蛋白和TSH水平。
TSH、游离T4、T3和T4的血清水平与菌血症、气管内细菌培养、动脉导管未闭、坏死性小肠结肠炎、脑超声检查变化、第28天的氧依赖以及氨茶碱、咖啡因、地塞米松、二醋吗啡和多巴胺的使用存在不同程度但显著的关联。
与之前对早产儿的认识相比,出生后因素与短暂性甲状腺素血症的关联更多。应考虑采用替代策略来纠正甲状腺素血症,而不是单纯依赖激素替代的直接治疗。可能需要通过降低个体疾病的发生率或严重程度来采取更间接的预防方法。同样,应评估那些干扰下丘脑 - 垂体 - 甲状腺轴的药物的替代品(例如用其他正性肌力药物替代多巴胺)。