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Department of Pediatrics, Division of Endocrinology (N.A., A.H.-K.), Sophia Childrens Hospital/Erasmus University Rotterdam, The Netherlands; Department of Endocrinology, St. Bartholomews and the Royal London School of Medicine and Dentistry (L.J., M.S., A.C.), London, United Kingdom; and Department of Epidemiology and Biostatistics (C.v.D., M.d.R.), Erasmus University Rotterdam, The Netherlands
Abstract
Low birth weight is associated with an increased risk in adult life
of type 2 diabetes, hypertension and cardiovascular disease (CVD). The
fetal insulin hypothesis postulates that genes involving insulin
resistance could effect birth weight and disease in later life
(Hattersley, 1999). Besides insulin, there is extensive evidence that
insulin-like growth factor-I and -II (IGF-I, IGF-II) play an important
role in fetal growth. We hypothesized that minor genetic variation in
the IGF-I gene could influence pre- and postnatal growth. Three
microsatellite markers located in the IGF-I gene in 124 short children
(height < -1.88 SDS) who were born small for gestational age (SGA)
and their parents were studied. SGA was defined as both a birth weight
and birth length below -1.88 SDS for gestational age. Two polymorphic
markers showed transmission disequilibrium. Allele 191 of the IGF1.PCR1
marker was transmitted more frequently from parent to child
(
2 = 4.8 and p = 0.02) and allele 198 of the 737/738
marker was transmitted less frequently from parent to child (
= 4.5
and p = 0.03). Children carrying the 191-allele had significantly lower
IGF-1 levels than children not carrying this allele (-1.1 SDS vs.
-0.05 SDS; p = 0.03). Also, head circumference SDS remained smaller in
children with allele 191 compared to children without allele 191 (-2.1
SDS vs. -0.9 SDS; p = 0.003). Our results show that genetically
determined low IGF-I levels may lead to a reduction in birth weight,
length and head circumference and to persistent short stature and small
head circumference in later life (proportionate small). Since low IGF-I
levels are associated with type 2 diabetes and CVD, we propose that the
IGF-I gene may provide a link between low birth weight and such
diseases in later life.
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