Mitchell M L, Hermos R J
New England Newborn Screening Program, University of Massachusetts Medical Center, Jamaica Plain, MA 02130, USA.
Clin Endocrinol (Oxf). 1998 Jun;48(6):757-60. doi: 10.1046/j.1365-2265.1998.00430.x.
Screening for congenital adrenal hyperplasia (CAH) in newborns has become a routine part of many programmes by measuring levels of 17 alpha-hydroxyprogesterone (17-OHP) in the newborn filter-paper blood specimen. Unfortunately, raised levels of 17-OHP, which are largely the consequence of cross-reacting metabolites, are also found in low birth weight, premature and ill neonates. We speculated that differences in concentrations of cortisol in the newborn screening specimen would aid in distinguishing between CAH positive and CAH negative infants among those with raised levels of 17-OHP.
Comparison of cortisol concentrations was made between newborns with CAH and those without but with raised 17-OHP levels.
Newborn filter-paper blood specimens from 31 infants with transient 17-OHP elevations and 16 infants with confirmed CAH were analysed for cortisol. In addition, assay performance was validated by comparing cortisol values obtained from dried whole blood on filter-paper with the corresponding plasma from 31 adults and six neonates.
Cortisol in filter-paper blood specimens was determined by adapting a commercial radioimmunoassay kit that had been designed for the determination of cortisol in serum.
The mean cortisol level in the CAH negative group was significantly higher than the mean value in the group with documented CAH (means 1190 +/- 795 nmol/l vs 627 +/- 210 nmol/l; P < 0.01). However, approximately half of the CAH negative infants had cortisol values that overlapped those from the CAH positive group. There was no relationship between the magnitude of the 17-OHP elevation and cortisol concentrations.
The measurements of cortisol in dried blood on filter-paper using a commercial radioimmunoassay kit has been shown to be reliable and simple to carry out. The level of cortisol in newborn blood specimens can be used to exclude some infants with elevated 17 alpha-hydroxyprogesterone levels from further testing for CAH. However, overlapping cortisol values between CAH positive and negative infants precludes the assay of cortisol from being used routinely as a reliable means of decision making.
通过检测新生儿滤纸血标本中17α-羟孕酮(17-OHP)水平,对新生儿先天性肾上腺皮质增生症(CAH)进行筛查已成为许多项目的常规部分。遗憾的是,出生体重低、早产及患病的新生儿中也会出现17-OHP水平升高的情况,这主要是交叉反应代谢产物所致。我们推测,新生儿筛查标本中皮质醇浓度的差异有助于在17-OHP水平升高的婴儿中区分CAH阳性和CAH阴性婴儿。
对患有CAH的新生儿与未患CAH但17-OHP水平升高的新生儿的皮质醇浓度进行比较。
对31例17-OHP短暂升高的婴儿和16例确诊为CAH的婴儿的新生儿滤纸血标本进行皮质醇分析。此外,通过比较从滤纸上的干全血获得的皮质醇值与31名成年人及6名新生儿的相应血浆,验证了检测性能。
采用一种专为测定血清中皮质醇设计的商用放射免疫分析试剂盒,对滤纸血标本中的皮质醇进行测定。
CAH阴性组的平均皮质醇水平显著高于确诊为CAH组的平均值(均值分别为1190±795 nmol/l和627±210 nmol/l;P<0.01)。然而,约一半的CAH阴性婴儿的皮质醇值与CAH阳性组的重叠。17-OHP升高幅度与皮质醇浓度之间无相关性。
使用商用放射免疫分析试剂盒测定滤纸上干血中的皮质醇已证明可靠且操作简单。新生儿血标本中的皮质醇水平可用于排除一些17α-羟孕酮水平升高的婴儿进行进一步的CAH检测。然而,CAH阳性和阴性婴儿之间皮质醇值的重叠使得皮质醇检测不能常规用作可靠的决策手段。