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. 2011 Sep 16;6(9):e24292. doi: 10.1371/journal.pone.0024292

Table 1. Analysis of the association of PTPN22 1858C>T SNP with RA patients and healthy subjects.

Genotype
Group C/C C/T T/T T Allele HWE (p)1 OR (95%CIs)2 Allelic p 3
Females RA patients (n = 313) (mean age: 55.7±13.7) 276 (91.6%) 36 (11.5%) 1 (0.3%) 38 (6.1%) 1.00 1.56 (0.95–2.55) 0.074
Healthy controls (n = 377) (mean age: 55.5±14.1) 348 (92.3%) 28 (7.4%) 1 (0.3%) 30 (4.0%) 0.45
Males RA patients (n = 83) (mean age: 59.7±12.2) 76 (91.6%) 7 (8.4%) 0 (0.0%) 7 (4.2%) 1.00 1.72 (0.54–5.52) 0.359
Healthy controls (n = 100) (mean age: 59.4±12.0) 95 (95.0%) 5 (5.0%) 0 (0.0%) 5 (2.5%) 1.00
All RA patients (n = 396) (mean age: 56.6±13.4) 352 (88.9%) 43 (10.9%) 1 (0.2%) 45 (5.7%) 1.00 1.58 (1.01–2.49) 0.045
Healthy controls (n = 477) (mean age: 56.3±14.0) 443 (92.9%) 33 (6.9%) 1 (0.2%) 35 (3.7%) 0.48
1

HWE: Hardy-Weinberg equilibrium.

2

Odds ratios expressed as carriers of T1858 allele vs. non-carriers considering healthy controls as control group.

3

Fisher's exact test of odds ratios.