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

Citation
P. Vanhaesebrouck et al., 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, Pediatric research, 36(1), 1994, pp. 71-76
Citations number
24
Categorie Soggetti
Pediatrics
Journal title
ISSN journal
00313998
Volume
36
Issue
1
Year of publication
1994
Part
1
Pages
71 - 76
Database
ISI
SICI code
0031-3998(1994)36:1<71:APOTPI>2.0.ZU;2-X
Abstract
N-terminal propeptide of type III procollagen (PIIINP) concentration w as measured in cord serum, amniotic fluid, and maternal serum from hig h-risk pregnancies. The fetal PIIINP variability was shown to be indep endent of the maternal serum PIIINP values. Although a highly signific ant 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 co ncentration in cord serum or amniotic fluid of small-for-gestational-a ge infants was significantly lower compared with that of appropriate-f or-gestational-age infants matched for postconceptional age. PIIINP as say may thus serve as a dynamic biochemical indicator of deviant fetal growth. The PIIINP results were also related to the severity or durat ion of intrauterine growth retardation, as indicated by significantly lower propeptide cord serum values in nonmalformed small-for-gestation al-age infants with small head circumference, known as an index for th e chronicity of fetal nutritional deprivation. Preeclampsia, maternal diabetes or smoking, and congenital anomalies appeared not to be assoc iated 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 pro peptides or their fragments usually are excreted by the fetal kidneys into the amniotic fluid. We suggest that determination of the PIIINP l ever in amniotic fluid or cord serum, obtained by amniocentesis and pe rcutaneous umbilical sampling, may be a helpful adjunctive biochemical parameter in future research protocols assessing fetuses at risk for intrauterine growth retardation.