Table 2 Association of UCHL1 S18Y polymorphism with sporadic Parkinson’s disease in a Japanese population
From: UCHL1 S18Y variant is a risk factor for Parkinson’s disease in Japan
n (%) | |||||
|---|---|---|---|---|---|
Model | Genotype | Cases (N = 229) | Controls (N = 357) | Crude OR (95 % CI) | Adjusted OR (95 % CI)* |
Co-dominant | CC | 61 (26.6) | 96 (26.9) | 1.00 | 1.00 |
CA | 98 (42.8) | 183 (51.3) | 0.84 (0.56 − 1.26) | 0.85 (0.56 − 1.30) | |
AA | 70 (30.6) | 78 (21.9) | 1.41 (0.90 − 2.23) | 1.41 (0.88 − 2.27) | |
Additive | 1.19 (0.94 − 1.50) | 1.19 (0.94 − 1.51) | |||
Dominant | 1.01 (0.70 − 1.47) | 1.02 (0.69 − 1.51) | |||
Recessive | 1.57 (1.08 − 2.30) | 1.57 (1.06 − 2.31) | |||