Positive associations between single nucleotide polymorphisms in the IGF2 gene region and body mass index in adult males

We previously demonstrated an association between the insulin-like growth factor 2 (IGF2) gene 3 ' -untranslated region (3 ' -UTR) ApaI polymorphism and body mass index (BMI) in over 2500 middle-aged Caucasoid males. In the same cohort, we have now tested association with 11 more markers, including seven novel single nucleotide polymorphisms (SNPs), spanning > 30 kb across the IGF2 gene. Three SNPs showed significant positive associations with BMI: 6815 AIT in the IGF2 P1 promoter (P = 0.00012, n = 2394) and the newly identified SNPs 1156 CIT in intron 2 (P = 0.017, n = 1567) and 1926 C/G in the 3 ' -UTR (P = 0.0062, n = 1872). There was strong pairwise linkage disequilibrium (LD) between the ApaI and 1926 C/G sites, whereas LD between ApaI and 6815 Al T, and between ApaI and 1156 TIC, was minimal. Univariately 6815 AIT, 1156 TIC and ApaI explained 1.03,1.02 and 0.67% of the variation in BMI. Multi-way analysis of variance (ANOVA) models showed that 6815 AIT and 1156 TIC explained a further 0.4 and 0.8% of the variation beyond that accounted for by ApaI and the association of 1926 C/G with BMI disappeared after adjustment. The 6815 AIT, 1156 TIC and ApaI markers in effect constitute independent affirmations of our original hypothesized candidate gene region. In a stepwise multi-way ANOVA model, all three terms were significantly independently associated with BMI. The total proportion of BMI variance explained by this model was 2.25%, strongly suggesting that IGF2 genetic variation is a significant determinant of body weight in middle-aged males.