Table 3. Two-way analyses of complement factor H 402 and rs11200638.
PAR% |
(95% CI) |
M-H test: p-value |
||||
Model for rs11200638 |
CFH 402 |
rs11200638 |
CFH 402 |
rs11200638 |
LRT p-value |
AIC value |
Full |
3.4 (0, 9.7) |
58.3 (50.5, 64.1) |
0.07 |
8.30E-08 |
0.03 |
221.8 |
Recessive |
4.6 (0, 10.7) |
44 (40.5, 54.0) |
0.23 |
6.20E-09 |
0.12 |
221.5 |
Multiplicative |
1.7 (0, 7.8) |
79.8 (73.0, 88.1) |
* |
* |
0.02 |
225.7 |
Dominant | 2.2 (0, 13.7) | 58.6 (43.9, 78.9) | 0.91 | 5.80E-04 | 0.1 | 246.9 |
Four genotypic models for rs11200638 are considered: Let r0, r1, and r2 be the marginal relative risks for genotypes GG, GA, and AA. Then, recessive model implies r0=r1; multiplicative model implies r1=r0r2; dominant model implies r2=r1; full model does not have any restriction on relative risks except that r0, r1, r2>0. The 95% confidence intervals (CI) of population attributable risk (PAR) were obtained via a bootstrap re-sampling method with 999 replicates. Mantel-Hanzel (M-H) tests are conducted for one SNP association adjusted for the other SNP; likelihood ratio tests (LRT) for joint single nucleotide polymorphism (SNP) association under a two-way multiplicative model: the relative risk (or OR) for any genotype pair (A, B) relative to the baseline pair (A0, B0) is the product of relative risk (or OR) of A relative to A0 and that of B relative to B0. AIC denotes the Akaike's information criterion to access goodness-of-fit for the rs11200638 model.