Table 5. ORs between NINJ2 haplotypes and the risk of dementia.
Co-dominant model | Additive model | |||||||||
Haplotype | Prevalence in controls, % | 0 copies | 1 copy | 2 copies | OR (95%CI) | |||||
Case/Control | OR | Case/Control | OR (95%CI) | p | Case/Control | OR (95%CI) | p | |||
AD (Global test p = 0.03) | ||||||||||
HAP1: AGAGG | 38.0 | 99/162 | 1.00 | 119/196 | 1.20 (0.82–1.74) | 0.35 | 51/61 | 1.30 (0.79–2.14) | 0.30 | 1.15 (0.91–1.46) |
HAP2: CAGGA | 23.8 | 169/241 | 1.00 | 99/161 | 0.98 (0.69–1.41) | 0.93 | 5/19 | 0.32 (0.11–0.94) | 0.04 | 0.83 (0.61–1.12) |
HAP3: CGGGG | 16.8 | 179/289 | 1.00 | 81/114 | 1.17 (0.80–1.71) | 0.42 | 7/14 | 0.67 (0.24–1.86) | 0.44 | 1.03 (0.75–1.42) |
HAP4: CAAGG | 10.0 | 221/335 | 1.00 | 43/70 | 0.83 (0.53–1.31) | 0.43 | 2/6 | 0.21 (0.04–1.18) | 0.08 | 0.72 (0.48–1.08) |
HAP5: CGAAG | 8.9 | 225/348 | 1.00 | 45/71 | 1.08 (0.69–1.70) | 0.74 | 4/2 | 2.99 (0.49–18.21) | 0.23 | 1.19 (0.79–1.78) |
VaD (Global test p = 0.70) | ||||||||||
HAP1: AGGGG | 38.0 | 45/162 | 1.00 | 54/198 | 1.19 (0.73–1.95) | 0.51 | 15/61 | 0.91 (0.45–1.87) | 0.82 | 1.01 (0.73–1.40) |
HAP2: CAAGA | 23.8 | 64/240 | 1.00 | 45/162 | 1.04 (0.65–1.67) | 0.84 | 6/19 | 1.31 (0.46–3.70) | 0.59 | 1.09 (0.74–1.59) |
HAP3: CGAGG | 16.8 | 81/291 | 1.00 | 32/113 | 1.17 (0.71–1.95) | 0.60 | 1/14 | 0.21 (0.03–1.76) | 0.15 | 0.92 (0.60–1.42) |
HAP4: CAGGG | 10.0 | 93/337 | 1.00 | 17/70 | 0.69 (0.37–1.32) | 0.25 | 3/6 | 0.78 (0.17–3.69) | 0.77 | 0.76 (0.46–1.27) |
HAP5: CGGAG | 8.9 | 86/348 | 1.00 | 28/71 | 1.42 (0.82–2.45) | 0.20 | 0/2 | NA | NA | 1.27 (0.75–2.15) |
Cumulative frequency | 97.5 |
Abbreviation: NA, not applicable.
All models were adjusted for age and gender.