| HPFS (n = 733) | NHS (n = 833) |  | ||||
---|---|---|---|---|---|---|---|
 | Number of cases/Total number with allele (%) | Age-adjusted OR [95% CI] | Multivariable OR* [95% CI] | Number of cases/Total number with allele (%) | Age-adjusted OR [95% CI] | Multivariable OR* [95% CI] | p-value for sex *SNP interaction |
For GFR <60 ml/min/1.73 m 2 | Â | Â | Â | Â | Â | Â | Â |
   AGT1R T573C (C-allele) | 54/480 (11%) | 0.68 [0.42, 1.09] | 0.60 [0.36, 1.00] | 68/569 (12%) | 1.11 [0.68, 1.82] | 0.96 [0.57, 1.61] | 0.21 |
   AGT1R A1166C (C-allele) | 51/346 (15%) | 1.59 [0.99, 2.49] | 1.63 [1.01, 2.65] | 50/402 (12%) | 1.18 [0.76, 1.83] | 1.28 [0.80, 2.04] | 0.54 |
   AGT M235T (Thr) | 57/469 (12%) | 0.98 [0.61, 1.56] | 0.91 [0.55, 1.49] | 68/527 (13%) | 1.62 [0.99, 2.69] | 1.46 [0.85, 2.50] | 0.25 |
For prevalent CHD | Â | Â | Â | Â | Â | Â | Â |
   AGT1R T573C (C-allele) | 133/480 (28%) | 1.26 [0.85, 1.85] | 1.36 [0.91, 2.02] | 148/569 (26%) | 1.07 [0.75, 1.53] | 1.02 [0.69, 1.49] | 0.45 |
   AGT1R A1166C (C-allele) | 105/346 (30%) | 1.62 [1.14, 2.29] | 1.57 [1.10, 2.24] | 99/402 (25%) | 0.84 [0.61, 1.16] | 0.85 [0.61, 1.20] | 0.008 |
   AGT M235T (Thr) | 120/469 (26%) | 0.95 [0.66, 1.35] | 0.92 [0.64, 1.33] | 154/527 (29%) | 1.72 [1.20, 2.47] | 1.66 [1.13, 2.43] | 0.03 |