Polymorphism in the IGF-I Gene: Clinical Relevance for Short Children Born Small for Gestational Age (SGA)
Nicolette Arends,
Linda Johnston,
Anita Hokken-Koelega,
Cornelia van Duijn,
Maria de Ridder,
Martin Savage and
Adrian Clark
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 adultlife
of type 2 diabetes, hypertension and cardiovascular disease(CVD). The
fetal insulin hypothesis postulates that genes involvinginsulin
resistance could effect birth weight and disease inlater life
(Hattersley, 1999). Besides insulin, there is extensiveevidence that
insulin-like growth factor-I and -II (IGF-I, IGF-II)play an important
role in fetal growth. We hypothesized thatminor genetic variation in
the IGF-I gene could influence pre-and postnatal growth. Three
microsatellite markers located inthe IGF-I gene in 124 short children
(height < -1.88 SDS)who were born small for gestational age (SGA)
and their parentswere studied. SGA was defined as both a birth weight
and birthlength below -1.88 SDS for gestational age. Two polymorphic
markersshowed transmission disequilibrium. Allele 191 of the IGF1.PCR1
markerwas transmitted more frequently from parent to child
(2 = 4.8and p = 0.02) and allele 198 of the 737/738
marker was transmittedless frequently from parent to child ( = 4.5
and p = 0.03).Children carrying the 191-allele had significantly lower
IGF-1levels than children not carrying this allele (-1.1 SDS vs.
-0.05SDS; p = 0.03). Also, head circumference SDS remained smallerin
children with allele 191 compared to children without allele191 (-2.1
SDS vs. -0.9 SDS; p = 0.003). Our results show thatgenetically
determined low IGF-I levels may lead to a reductionin birth weight,
length and head circumference and to persistentshort stature and small
head circumference in later life (proportionatesmall). Since low IGF-I
levels are associated with type 2 diabetesand CVD, we propose that the
IGF-I gene may provide a link betweenlow birth weight and such
diseases in later life.
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