Variation at the Insulin Gene VNTR (Variable Number Tandem Repeat) Polymorphism and Early Growth
Studies in a Large Finnish Birth Cohort
- Amanda J. Bennett1,
- Ulla Sovio2,
- Aimo Ruokonen3,
- Hannu Martikainen4,
- Anneli Pouta5,
- Saara Taponen345,
- Anna-Liisa Hartikainen4,
- Vanessa J. King2,
- Paul Elliott2,
- Marjo-Riitta Järvelin25 and
- Mark I. McCarthy16
- 1Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Oxford, U.K
- 2Department of Epidemiology and Public Health, Imperial College (St. Mary’s Campus), London, U.K
- 3Department of Clinical Chemistry, University of Oulu, Oulu, Finland
- 4Department of Obstetrics and Gynaecology, University of Oulu, Oulu, Finland
- 5Department of Public Health Science and General Practice, University of Oulu, Oulu, Finland
- 6Wellcome Trust Centre for Human Genetics, Churchill Hospital, Oxford, U.K
- Address correspondence and reprint requests to Prof. Mark McCarthy, Robert Turner Professor of Diabetes, Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital Site, Old Road, Headington, Oxford, OX3 7LJ, U.K. E-mail: mark.mccarthy{at}drl.ox.ac.uk
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.
- ALSPAC, Avon Longitudinal Study of Parents and Children
- ARMS, amplification refractory mutation system
- GDM, gestational diabetes mellitus
- NFBC66, Northern Finland Birth Cohort of 1966
- VNTR, variable number of tandem repeats
Footnotes
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- Accepted April 26, 2004.
- Received February 2, 2004.
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