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
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
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.