Kdr. Setchell et al., Isoflavone content of infant formulas and the metabolic fate of these phytoestrogens in early life, AM J CLIN N, 68(6), 1998, pp. 1453S-1461S
Soy-based infant formulas have been in use for >30 y. These formulas are ma
nufactured from soy protein isolates and contain significant amounts of phy
toestrogens of the isoflavone class. As determined by HPLC, the isoflavone
compositions of commercially available formulas are similar qualitatively a
nd quantitatively and are consistent with the isoflavone composition of soy
protein isolates. Genistein, found predominantly in the form of glycosidic
conjugates, accounts for > 65% of the isoflavones in soy-based formulas. T
otal isoflavone concentrations of soy-based formulas prepared for infant fe
eding range from 32 to 47 mg/L, whereas isoflavone concentrations in human
breast milk are only 5.6 +/- 4.4 mu g/L ((x) over bar +/- SD, ia = 9). Infa
nts fed soy-based formulas are therefore exposed to 22-45 mg isoflavones/d
(6-11 mg.kg body wt(-1).d(-1)), whereas the intake of these phytoestrogens
from human milk is negligible (<0.01 mg/d). The metabolic fate of isoflavon
es from soy-based infant formula is described. Plasma isoflavone concentrat
ions reported previously for 4-mo-old infants fed soy-based formula were 65
4-1775 mu g/L ((x) over bar: 979.7 mu g/L; Lancet 1997:350;23-7), significa
ntly higher than plasma concentrations of infants fed either cow-milk formu
la ((x) over bar +/- SD: 9.4 +/- 1.2 mu g/L) or human breast milk (4.7 +/-
1.3 mu g/L). The high steady state plasma concentration of isoflavones in i
nfants fed soy-based formula is explained by reduced intestinal biotransfor
mation, as evidenced by low or undetectable concentrations of equol and oth
er metabolites, and is maintained by constant daily exposure from frequent
feeding. Isoflavones circulate at concentrations that are 13 000-22000-fold
higher than plasma estradiol concentrations in early life. Exposure to the
se phytoestrogens early in life may have long-term health benefits for horm
one-dependent diseases.