عنوان به زبان ديگر :
Insulin Gene Variable Number of Tandem Repeat Genotype, Early Growth and Glucose Metabolism in Adult Life
پديد آورندگان :
Eriksson J. نويسنده , Osmond C. نويسنده , Forsen J. نويسنده , Kajantie E . نويسنده , Barker De JP. نويسنده , Laakso M. نويسنده
چكيده لاتين :
The predisposition to type 2 diabetes is T programmed early in life and genotypes
promoting survival during nutritional
adversity could increase the risk
of type 2 diabetes. The insulin gene and variation
in the insulin gene variable number of tandem
repeats (VNTR) polymorphism has been
suggested to modify birth size and diabetes susceptibility.
Materials and Methods: We assessed the association
between the insulin gene VNTR genotypes,
early growth and glucose and insulin metabolism
in adult life in 488 subjects participating in
the Helsinki Birth Cohort Study.
Results: Body size at birth did not differ significantly
between the INS VNTR genotypes. One
additional type III allele was associated with a
13 g decrease (95% CI -55 to 81 g; p=O.7) in birth
weight. Fasting glucose concentration was highest
in the carriers of the III/Ill genotype. The
cumulative incidence of type 2 diabetes did not
differ between the genotypes. Interactions between
birth size and insulin VNTR genotype in
relation to fasting glucose (p for interaction =
0.08 for birth weight, p=0.05 for birth length) and
2-hour insulin (p for interaction =0.04) were ob-
served.
Conclusions: These interactions between body
size at birth and genotype reflect interactions between
the insulin VNTR gene and the intrauterine
environment. Our findings are consistent
with the hypothesis of developmental plasticity,
where one genotype can give rise to different
phenotypes dependent on the early environment.