In WHII a set of non-redundant IRS1 SNPs independently associated with T2D was determined by variable selection, Pictilisib purchase using stepwise regression based on the Bayesian information criterion [19]. An additive genetic model was assumed. Of the 23 SNPs, 18 with p < 0.25 on univariate analysis were initially selected for possible inclusion in the multivariate model. Statistically significance was taken as p < 0.01. Following the suggestion of Rothman [20], this more conservative p-value was used in preference to correcting for multiple comparisons. Baseline clinical, biochemical,

and the genetic characteristics of the subjects in WHII and NPHSII are presented in Supplementary Table 3. Subjects who went on to develop T2D were more likely to be obese and hypertensive, and in WHII had, as expected, higher baseline fasting glucose and insulin levels, higher percentage of HbA1c and a higher HOMA-IR

index (all p < 0.001). There were no significant genotype differences between T2D cases and controls; however, in WHII the rs2943641T allele was associated with lower fasting insulin (p = 0.04) and HOMA-IR (p = 0.03) in a mixed regression model over all study phases while adjusting for age, gender, BMI and study phase ( Supplementary Table 4). The overall characteristics of the T2D patients in UDACS, EDS and PREDICT by ethnic group and rs2943641 genotype, are presented in Supplementary Tables 5 and 6. In comparison to European whites, patients of Indian Asian origin had an earlier age of onset of the disease, a lower prevalence of obesity E7080 mouse and were less frequently smokers and carriers of the rs2943641T allele (Supplementary Table 5). No differences in any baseline biochemical measures, including fasting glucose and HbA1c, were observed across genotypes in the two ethnic groups (Supplementary Table 6). In EARSII, there was no ‘case’/‘control’ heterogeneity in age, BMI, BP, fasting glucose or rs2943641 genotype distribution

(Supplementary Table 3) and therefore, ‘cases’ and Meloxicam ‘controls’ were combined in subsequent analyses. No significant differences across genotypes for any of the fasting biochemical variables were observed in this cohort of young individuals; however, rs2943641T allele was associated with lower insulin levels after OGTT (Fig. 1). The effect of rs2943641T appeared to be dominant, with T-allele carriers having area under the curve (AUC) for insulin 13.3% lower than CC homozygotes (p = 0.003). The difference among genotypes was significant at 60 and at 90 min after the OGTT (p = 0.004 and p = 0.03, respectively, Fig. 1). There was no evidence for heterogeneity between ‘cases’ and ‘controls’ for AUCinsulin (p = 0.47), nor were any differences between genotype groups for AUCglucose ( Supplementary Table 7).