Table 4.
Univariate Five-State Markov Model for AMD Progression
SNP | Gene | Effective Allele/Genotype | Worse Eye Transition |
|||||||
---|---|---|---|---|---|---|---|---|---|---|
1 → 2 |
2 → 3 |
3 → 4 |
3 → 5 |
|||||||
HR* | P | HR* | P | HR* | P | HR* | P | |||
rs1061170 | CFH | C | 1.01 (0.89, 1.16) | 0.83 | 1.26 (1.09, 1.45) | 1.3 × 10−3 | 1.62 (1.37, 1.91) | 8.4 × 10−9 | 1.61 (1.37, 1.89) | 5.3 × 10−9 |
rs10490924 | ARMS2/HTRA1 | T | 1.14 (0.98, 1.33) | 0.09 | 1.4 (1.2, 1.64) | 2.8 × 10−5 | 1.51 (1.28, 1.78) | 7.6 × 10−7 | 1.52 (1.29, 1.78) | 3.4 × 10−7 |
rs9332739 | C2 | C† | 0.9 (0.66, 1.23) | 0.52 | 0.82 (0.55, 1.21) | 0.31 | 0.56 (0.31, 1.03) | 0.06 | 0.44 (0.23, 0.86) | 0.02 |
rs641153 | CFB | T† | 0.91 (0.72, 1.16) | 0.45 | 0.79 (0.59, 1.07) | 0.13 | 0.64 (0.42, 0.97) | 0.03 | 0.53 (0.34, 0.82) | 4.3×10−3 |
rs2230199 | C3 | G | 1.11 (0.95, 1.29) | 0.18 | 1.2 (1.01, 1.42) | 0.03 | 1.36 (1.13, 1.63) | 9.4×10−4 | 1.3 (1.09, 1.55) | 4.3×10−3 |
rs10033900 | CFI | T | 1.13 (1, 1.28) | 0.05 | 1.03 (0.89, 1.18) | 0.70 | 1.29 (1.09, 1.52) | 3.2×10−3 | 0.95 (0.8, 1.11) | 0.49 |
rs10468017 | LIPC | TT† | 0.71 (0.5, 1) | 0.05 | 0.85 (0.56, 1.28) | 0.44 | 0.81 (0.5, 1.31) | 0.39 | 0.64 (0.38, 1.08) | 0.10 |
rs9621532 | TIMP3 | C† | 0.99 (0.73, 1.34) | 0.94 | 1.06 (0.77, 1.47) | 0.71 | 0.69 (0.44, 1.08) | 0.11 | 0.71 (0.47, 1.09) | 0.12 |
rs3764261 | CETP | A | 1.08 (0.94, 1.23) | 0.28 | 1.03 (0.89, 1.2) | 0.68 | 1 (0.84, 1.19) | 0.99 | 1.27 (1.08, 1.49) | 4.6×10−3 |
rs1883025 | ABCA1 | T | 0.82 (0.71, 0.95) | 7.8×10−3 | 0.79 (0.66, 0.95) | 9.7×10−3 | 1 (0.82, 1.21) | 0.97 | 1.02 (0.85, 1.23) | 0.81 |
rs13095226 | COL8A1 | C† | 1.13 (0.91, 1.4) | 0.29 | 0.67 (0.49, 0.9) | 8.0×10−3 | 1.55 (1.18, 2.04) | 1.7×10−3 | 1.36 (1.04, 1.79) | 0.03 |
APOE† | APOE | E4† | 0.98 (0.8, 1.21) | 0.87 | 0.91 (0.7, 1.17) | 0.47 | 0.79 (0.58, 1.07) | 0.12 | 0.88 (0.66, 1.17) | 0.39 |
HR, hazard ratio for a specific transition.
P value is bold for variables significantly (P ≤ 0.05) associated with a specific transition.
Genotypes are combined at the marked SNPs, which are coded 0 for subjects without the effective allele/genotype and 1 for subjects with the effective allele/genotype. APOE haplotypes were defined by alleles in rs7412 and rs429358. SNPs not marked are coded by the number of effective alleles (0, 1, or 2).