Umbilical cord blood
samples were collected from 12,804 consecutive deliveries, and cord
plasma samples were collected from 585 singleton infants born in
Norway at term after uncomplicated pregnancies. These were analyzed
for plasma leptin, IGF-I, IGFBP-1 and IGFBP-3. Data were analyzed
following log transformation of IGFBP-1 and leptin values. Linear
regression analysis was used to determine the contribution of maternal
and infant factors to umbilical levels of these hormones. The mean
age of the mothers of these infants was 28 years. Seven percent had
smoked at the beginning of the pregnancy, and 36 percent were
primiparous. Male infants had a higher birth weight and length than
girls, but girls had a higher ponderal index. Leptin and IGF-I levels
were higher in the cord blood of female infants than in males. None of
the maternal factors which were analyzed, including pre-pregnancy
weights, smoking, or number of previous pregnancies were significantly
associated with levels of cord leptin. IGF-I, IGFBP-3, and leptin
increased proportionately with increasing birth weight. Levels of
IGF-I and leptin were the strongest predictors of both birth weight
and birth length, and were independent of length of gestation,
maternal age, parity, pre-pregnancy weight, smoking and offspring
sex.
The authors conclude
that their data suggest that the sexual dimorphism in the regulation
of leptin and IGF concentrations, which previously was demonstrated in
later childhood, may already be established at birth. They also
suggest a possible role for leptin and/or the IGF–I system in relation
to birth size and to the risk of diseases such as non-insulin
dependent diabetes and cardiovascular disease which have been shown to
be frequent in low birth weight infants.
Editor’s Comment:
These findings have important implications for understanding the
relationship between low birth weight and adult morbidity - especially
cardiovascular disease, hypertension, and type 2
diabetes. It would appear that leptin, IGF-I, and IGFBP-I,
which have been shown to be important factors in growth in utero, may
be important in understanding the risk of developing these adult
diseases. It would be very important to follow a cohort of children
from birth through adulthood with serial measurements of IGF-I,
IGFBP-3, and leptin in order to better understand how these factors
change over time and how they might contribute to the development of
serious adult disorders. Studies such as those by
Vatten et al in Norway support the importance of conducting
such difficult epidemiological studies.
William L. Clarke,
MD