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. Author manuscript; available in PMC: 2007 Jan 4.
Published in final edited form as: N Engl J Med. 2006 Jul 20;355(3):241–250. doi: 10.1056/NEJMoa062418

Table 2.

Incidence of Diabetes According to Genotype at the rs12255372 and rs7903146 Variants.*

Variable No. of Participants Genotype at rs12255372 Hazard Ratio for GT vs. GG (95% CI) P Value GT P Value Hazard Ratio for TT vs. GG (95% CI) P Value TT P Value PAR
GG GT TT
no. of cases of diabetes (cases/100 person-yr)
Overall cohort 2951 302 (7.4) 260 (8.0) 69 (10.6) 1.08 (0.92–1.29) 0.35 1.53 (1.17–2.01) 0.002 0.11
Whites 1657 140 (6.8) 165 (8.0) 45 (10.8) 1.19 (0.94–1.50) 0.14 1.67 (1.18–2.37) 0.004 0.14
African Americans 600 67 (8.6) 56 (8.6) 16 (10.3) 1.02 (0.71–1.47) 0.90 0.50 1.24 (0.70–2.17) 0.46 0.35 0.13
Hispanics 489 62 (7.6) 30 (6.7) <15 (10.2) 0.83 (0.53–1.31) 0.42 0.18 1.70 (0.75–3.87) 0.21 0.93 0.10
Asians 124 20 (8.0) <15 (7.7) <15 (13.0) 0.88 (0.36–2.15) 0.78 0.58 1.42 (0.17–11.7) 0.75 0.95 0.18
American Indians 81 <15 (6.6) <15 (11.8) <15 (0.0) 1.93 (0.39–9.63) 0.42 0.58 NA NA 0.97 NA
Genotype at rs7903146 Hazard Ratio for CT vs. CC (95%3CI) P Value CT P Value Hazard Ratio for TT vs. CC (95% CI) P Value TT P Value PAR
CC CT TT
no. of cases of diabetes (cases/100 person-yr)
Overall cohort 2983 305 (7.6) 255 (7.6) 77 (10.8) 1.00 (0.84–1.19) 0.99 1.55 (1.20–2.01) <0.001 0.06
Whites 1671 147 (7.3) 153 (7.4) 51 (10.9) 1.03 (0.81–1.30) 0.82 1.62 (1.16–2.25) 0.004 0.05
African Americans 605 64 (8.5) 62 (8.9) <15 (9.7) 1.09 (0.76–1.56) 0.65 0.82 1.20 (0.66–2.17) 0.55 0.36 0.10
Hispanics 497 61 (7.4) 29 (6.6) <15 (12.7) 0.89 (0.56–1.41) 0.62 0.60 2.26 (1.14–4.50) 0.02 0.46 0.18
Asians 128 22 (9.2) <15 (6.4) <15 (8.9) 0.55 (0.23–1.33) 0.19 0.26 0.92 (0.11–7.48) 0.94 0.66 −0.12
American Indians 82 <15 (6.7) <15 (7.5) <15 (0.0) 1.15 (0.35–3.78) 0.82 0.84 NA NA 0.97 NA
*

CI denotes 95 percent confidence interval, PAR population attributable risk (calculated with data from the placebo group), and NA not available because of insufficient data.

In instances where the number of cases is less than 15, exact numbers were not reported to protect the confidentiality of participants, per DPP publication policy.

The P value is for the interaction between the genotype and the race or ethnic group, with the largest groups (whites and those who were homozygous for the major allele) serving as the reference group.