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早产儿血浆皮质醇与慢性肺病的关联

Association of plasma cortisol and chronic lung disease in preterm infants.

作者信息

Banks B A, Stouffer N, Cnaan A, Ning Y, Merrill J D, Ballard R A, Ballard P L

机构信息

Department of Pediatrics, University of Pennsylvania and Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104-4318, USA.

出版信息

Pediatrics. 2001 Mar;107(3):494-8. doi: 10.1542/peds.107.3.494.

Abstract

BACKGROUND

It has been suggested that preterm infants may have developmental immaturity of the hypothalamic-pituitary-adrenal axis, and that decreased cortisol response to stress increases risk of chronic lung disease (CLD) secondary to inflammatory lung injury.

METHODS

To investigate the relationship between endogenous corticosteroid and CLD, we measured plasma cortisol during the first 28 days of life in a subset of neonates in the North American Thyrotropin-Releasing Hormone (TRH) Collaborative Trial. Analyses were performed on 314 infants, 24 to 32 weeks' gestation, whose mothers received 1 or 2 courses of antenatal corticosteroids plus TRH or placebo.

RESULTS

Mean cortisol was 3.1 microg/dL (range: 0.1-17.9) at birth, reached maximal levels at 24 hours (19.4 microg/dL, range: 0.8-124.6), and decreased to 5.9 microg/dL (range: 0.2-24.7) at 14 to 28 days of age; levels during the first week were not associated with gestational age. The Clinical Risk Index for Babies (CRIB), a neonatal assessment tool that is correlated with risk of mortality, was positively associated with cortisol level on days 1 and 3 through 7. TRH versus placebo treatment did not influence cortisol levels at any time point. To examine the relationship between cortisol and adverse outcome of death or CLD at 36 weeks' postmenstrual age (CLD36), logistic regression models adjusting for known contributing clinical factors (gestational age and CRIB score) were fit. There was a statistically borderline negative association between median cortisol level at 3 to 7 days and CLD36. After adjusting for gestational age and CRIB score, the predicted probability of CLD36 was only minimally influenced by the cortisol concentration.

CONCLUSION

In preterm infants, basal plasma cortisol concentration during the first week is a weak predictor for CLD36. Possible benefits as well as risks of supplemental, low-dose cortisol treatment of high-risk preterm infants remain to be determined.

摘要

背景

有人提出,早产儿可能存在下丘脑 - 垂体 - 肾上腺轴发育不成熟的情况,且皮质醇对应激的反应降低会增加因炎症性肺损伤继发慢性肺病(CLD)的风险。

方法

为了研究内源性皮质类固醇与CLD之间的关系,我们在北美促甲状腺激素释放激素(TRH)协作试验的一部分新生儿出生后的前28天内测量了血浆皮质醇。对314名妊娠24至32周的婴儿进行了分析,这些婴儿的母亲接受了1或2个疗程的产前皮质类固醇加TRH或安慰剂治疗。

结果

出生时平均皮质醇为3.1微克/分升(范围:0.1 - 17.9),在24小时时达到最高水平(19.4微克/分升,范围:0.8 - 124.6),并在14至28日龄时降至5.9微克/分升(范围:0.2 - 24.7);第一周内的水平与胎龄无关。婴儿临床风险指数(CRIB)是一种与死亡风险相关的新生儿评估工具,在第1天和第3天至第7天与皮质醇水平呈正相关。TRH与安慰剂治疗在任何时间点都不影响皮质醇水平。为了研究皮质醇与月经后36周时死亡或CLD不良结局(CLD36)之间的关系,我们建立了调整已知相关临床因素(胎龄和CRIB评分)的逻辑回归模型。在3至7天时的中位皮质醇水平与CLD36之间存在统计学上接近显著的负相关。在调整胎龄和CRIB评分后,CLD36的预测概率仅受到皮质醇浓度的轻微影响。

结论

在早产儿中,第一周的基础血浆皮质醇浓度是CLD36的一个弱预测指标。补充低剂量皮质醇治疗高危早产儿的潜在益处和风险仍有待确定。

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