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高危妊娠脐带血和羊水中III型前胶原氨基端前肽:一种动态评估胎儿生长异常的生化方法

Aminoterminal propeptide of type III procollagen in cord blood and amniotic fluid of high-risk pregnancies: a biochemical approach to the dynamic assessment of deviant fetal growth.

作者信息

Vanhaesebrouck P, Kint J, Van Kets H, Govaert P, Smets K, Defoort P, Leroy J

机构信息

Department of Pediatrics and Neonatal Medicine, University Hospital Gent, Belgium.

出版信息

Pediatr Res. 1994 Jul;36(1 Pt 1):71-6. doi: 10.1203/00006450-199407001-00012.

Abstract

N-terminal propeptide of type III procollagen (PIIINP) concentration was measured in cord serum, amniotic fluid, and maternal serum from high-risk pregnancies. The fetal PIIINP variability was shown to be independent of the maternal serum PIIINP values. Although a highly significant negative correlation was found between the fetal propeptide level and gestational age in both appropriate-for-gestational-age neonates (n = 504) and small-for-gestational-age infants (n = 98), the PIIINP concentration in cord serum or amniotic fluid of small-for-gestational-age infants was significantly lower compared with that of appropriate-for-gestational-age infants matched for postconceptional age. PIIINP assay may thus serve as a dynamic biochemical indicator of deviant fetal growth. The PIIINP results were also related to the severity or duration of intrauterine growth retardation, as indicated by significantly lower propeptide cord serum values in nonmalformed small-for-gestational-age infants with small head circumference, known as an index for the chronicity of fetal nutritional deprivation. Preeclampsia, maternal diabetes or smoking, and congenital anomalies appeared not to be associated with any alteration of fetal propeptide concentration, provided they did not cause fetal growth deceleration. The finding of extremely high cord serum PIIINP values in six newborn infants with the Potter malformation sequence led to the speculation that large amounts of propeptides or their fragments usually are excreted by the fetal kidneys into the amniotic fluid. We suggest that determination of the PIIINP level in amniotic fluid or cord serum, obtained by amniocentesis and percutaneous umbilical sampling, may be a helpful adjunctive biochemical parameter in future research protocols assessing fetuses at risk for intrauterine growth retardation.

摘要

在高危妊娠的脐带血血清、羊水和母体血清中检测了III型前胶原N端前肽(PIIINP)的浓度。结果显示,胎儿PIIINP的变异性与母体血清PIIINP值无关。尽管在适于胎龄儿(n = 504)和小于胎龄儿(n = 98)中,胎儿前肽水平与胎龄之间均发现了高度显著的负相关,但小于胎龄儿脐带血血清或羊水中的PIIINP浓度与按孕龄匹配的适于胎龄儿相比显著降低。因此,PIIINP检测可作为胎儿生长异常的动态生化指标。PIIINP结果还与宫内生长迟缓的严重程度或持续时间有关,小头围的非畸形小于胎龄儿脐带血血清前肽值显著降低,这被视为胎儿营养剥夺慢性化的指标。先兆子痫、母体糖尿病或吸烟以及先天性异常,只要不导致胎儿生长减速,似乎与胎儿前肽浓度的任何改变均无关联。在6例患有波特序列征的新生儿中发现脐带血血清PIIINP值极高,这使得人们推测大量的前肽或其片段通常由胎儿肾脏排入羊水中。我们建议,通过羊膜腔穿刺术和经皮脐血取样获得的羊水或脐带血血清中PIIINP水平的测定,可能是未来评估有宫内生长迟缓风险胎儿的研究方案中一个有用的辅助生化参数。

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