A. Malamitsi-puchner et al., Heparin-binding angiogenic factors (basic fibroblast growth factor and vascular endothelial growth factor) in early neonatal life, PEDIAT RES, 45(6), 1999, pp. 877-880
This study investigated whether serum levels of the potent angiogenic facto
rs basic fibroblast growth factor (bFGF) and vascular endothelial growth fa
ctor (VEGF), which are abundantly produced in utero by the placenta and fet
al tissues, change after birth at term, consequent to diminished angiogenic
but increased adaptational demands in extrauterine life. Moreover, whether
serum levels of the above factors correlate with sex, birth weight, or mod
e of delivery was also evaluated. One milliliter of blood was drawn from 30
healthy, appropriate for gestational age, full-term infants on d 1 (N1) an
d 4 (N4) postnatally. In 10 of the above cases maternal and umbilical cord
blood samples were also drawn. Serum was analyzed by enzyme immunoassays, u
sing commercial kits. Levels of bFGF and VEGF were significantly lower in m
aternal serum than in umbilical cord (p = 0.02 and 0.036, respectively) or
N1 (p = 0.009 and 0.006, respectively) and N4 serum (p = 0.009 and 0.006, r
espectively). Levels of bFGF in umbilical cord serum did not differ signifi
cantly from those in N1 and N4. In contrast, levels of VEGF rose in N1, dif
fering significantly from levels in umbilical cord serum (p = 0.008). Both
factors did not change from N1 to N4. Neither bFGF nor VEGF serum levels de
pended on sex, mode of delivery, or birth weight. In conclusion, bFGF level
s in neonates do not differ from levels in fetuses, possibly reflecting dim
inished angiogenesis in extrauterine life, which already has started in ute
ro. On the contrary, neonatal levels of VEGF rise significantly after birth
, possibly signifying adaptation demands, in addition to angiogenesis, as V
EGF is also considered a regulator of normal function.