Variation at the Insulin Gene VNTR (Variable Number Tandem Repeat) Polymorphism and Early Growth

Author:

Bennett Amanda J.1,Sovio Ulla2,Ruokonen Aimo3,Martikainen Hannu4,Pouta Anneli5,Taponen Saara345,Hartikainen Anna-Liisa4,King Vanessa J.2,Elliott Paul2,Järvelin Marjo-Riitta25,McCarthy Mark I.16

Affiliation:

1. Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford, U.K

2. Department of Epidemiology and Public Health, Imperial College (St. Mary’s Campus), London, U.K

3. Department of Clinical Chemistry, University of Oulu, Oulu, Finland

4. Department of Obstetrics and Gynaecology, University of Oulu, Oulu, Finland

5. Department of Public Health Science and General Practice, University of Oulu, Oulu, Finland

6. Wellcome Trust Centre for Human Genetics, Churchill Hospital, Oxford, U.K

Abstract

Variation at the insulin gene (INS-)VNTR (variable number of tandem repeats) minisatellite polymorphism has been reported to be associated with both early growth and adult metabolic phenotypes. However, the samples studied have been small and the relationship between INS-VNTR variation and parameters of early growth inconsistent, with four previous studies producing conflicting results. We have studied the relationship between INS-VNTR class (measured by genotyping the nearby −23HphI variant with which it is in tight linkage disequilibrium) and early growth in 5,646 members of the Northern Finnish Birth Cohort of 1966. Comparing class III homozygotes with other genotypes using multivariate linear regression analysis, we found no significant associations with any early growth measure (birth weight, birth length, ponderal index, and head circumference at 1 year), even after stratifying subjects by growth trajectory during infancy and/or birth order. For example, among infants with limited postnatal growth realignment (n = 2,470), class III/III infants were no heavier at birth (difference [±SE] in the means [fully adjusted], 58 ± 51 g; P = 0.26) than class I/− infants. No significant associations were detected following reanalysis with an additive model (for example, for birth weight, β = 20 g [95% CI −3 to 44], P = 0.09). Studies of this large population-based cohort have failed to generate convincing evidence that INS-VNTR variation influences early growth.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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