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. 2016 Mar 10;2:16004. doi: 10.1038/npjparkd.2016.4

Table 2. Association between rs6812193 and rs6825004 genotypes and Parkinson’s disease.

Status Controls (n=272)
PD Cases (n=548)
P-value for PD risk OR for PD (95% CI) a
  N (%) GCase enzymatic activity b μmol/l/h (s.d.) N (%) GCase enzymatic activity b μmol/l/h (s.d.)
rs6812193
 C/C 115 (42.3%) 11.97 (3.31) 273 (49.8%) 11.82 (3.16) 0.057 Reference
             
 C/T 123 (45.2%) 11.96 (2.90) 229 (41.8%) 11.70 (3.09)   0.52 (0.30–0.89); P=0.018
 T/T 34 (12.5%) 12.07 (4.43) 46 (8.4%) 11.98 (3.10)   0.62 (0.36–1.07); P=0.086
 C 353 (64.8%)   775 (70.7%)   0.0175 0.71 (0.56–0.90); P=0.004c
 T 191 (35.2%)   321 (29.3%)      
             
rs6825004 d
 C/C 125 (46.1%) 11.94 (3.35) 243 (44.4%) 11.63 (2.88) 0.562 Reference
             
 C/G 115 (42.4%) 11.90 (3.22) 229 (41.9%) 11.97 (3.42)   1.03 (0.74–1.45); P=0.833
 G/G 31 (11.4%) 12.42 (3.33) 75 (13.7%) 11.76 (3.04)   0.79 (0.48–1.30); P=0.788
 C 365 (67.3%)   715 (65.3%)   0.438 1.17 (0.93–1.47); P=0.182c
 G 177 (32.7%)   379 (34.7%)      

Abbreviations: CI, confidence interval; OR, odds ratio; PD, Parkinson's disease.

a

OR calculated in models adjusted for age, gender, LRRK2 and GBA mutation status.

b

There was no difference in GCase activity among the genotypes, either in controls or in PD cases. Values presented here after excluding GBA and LRRK2 p.G2019S carriers.

c

Model included sex, age, rs6812193 genotype, and rs6825004 genotype.

d

rs6825004 was missing on one PD and one control participant.