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. 2020 Oct 3;17(19):7247. doi: 10.3390/ijerph17197247

Table 5.

Odds ratios (ORs) and 95% confidence intervals (CIs) of clinical status and HMGB1 rs1360485 genotypic frequencies in 579 patients with prostate cancer.

Variable Genotypic Frequencies
rs1360485 TT (N = 347) TC + CC (N = 232) OR (95% CI) p-Value
PSA at diagnosis (ng/mL)
≤10 161 (46.4%) 109 (47.0%) 1.00 p = 0.890
>10 186 (53.6%) 123 (53.0%) 0.977 (0.700–1.363)
Pathologic Gleason grade group
1 + 2 + 3 299 (86.2%) 185 (79.7%) 1.00 p = 0.041 *
4 + 5 48 (13.8%) 47 (20.3%) 1.583 (1.017–2.462)
Clinical T stage
1 + 2 302 (87.0%) 199 (85.8%) 1.00 p = 0.664
3 + 4 45 (13.0%) 33 (14.2%) 1.113 (0.686–1.805)
Pathologic T stage
2 197 (56.8%) 109 (47.0%) 1.00 p = 0.021 *
3 + 4 150 (43.2%) 123 (53.0%) 1.482 (1.061–2.070)
Pathologic N stage
N0 326 (93.9%) 204 (87.9%) 1.00 p = 0.011 *
N1 21 (6.1%) 28 (12.1%) 2.131 (1.178–3.852)
Seminal vesicle invasion
No 279 (80.4%) 173 (74.6%) 1.00 p = 0.096
Yes 68 (19.6%) 59 (25.4%) 1.399 (0.941–2.081)
Perineural invasion
No 97 (28.0%) 58 (25.0%) 1.00 p = 0.431
Yes 250 (72.0%) 174 (75.0%) 1.164 (0.797–1.700)
Lymphovascular invasion
No 296 (85.3%) 186 (80.2%) 1.00 p = 0.105
Yes 51 (14.7%) 46 (19.8%) 1.435 (0.926–2.226)
D’Amico classification
Low/Intermediate risk 178 (51.3%) 102 (44.0%) 1.00 p = 0.084
High risk 169 (48.7%) 130 (56.0%) 1.342 (0.961–1.875)

The ORs and their 95% CIs were estimated by logistic regression models. * p-value < 0.05 = statistically significant.