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. 2017 May 10;2017:4191365. doi: 10.1155/2017/4191365

Table 3.

Distributions of IL-31 SNPs among cases and controls and their associations with DCM susceptibility.

Genotype rs4758680 Genotype rs7977932
Cases
n (%)
Controls
n (%)
OR (95%CI) P value Cases
n (%)
Controls
n (%)
OR (95%CI) P value
Model
 Codominant CC 275 (83.1%) 361 (73.2%) 1.00 CC 271 (81.9%) 401 (81.3%) 1.00
CA 43 (13.0%) 114 (23.1%) 0.50 (0.34–0.72) 0.001 CG 56 (16.9%) 87 (17.6%) 1.05 (0.73–1.52) 0.930
AA 13 (3.9%) 18 (3.6%) 0.95 (0.46–1.96) GG 4 (1.2%) 5 (1.0%) 0.84 (0.22–3.17)

 Dominant CC 275 (83.1%) 361 (73.2%) 1.00 CC 271 (81.9%) 401 (81.3%) 1.00
CA/AA 56 (16.9%) 132 (26.8%) 0.56 (0.39–0.79) <0.001 CG/GG 60 (18.1%) 92 (18.7%) 1.04 (0.72–1.49) 0.850

 Recessive CC/CA 318 (96.1%) 475 (96.3%) 1.00 CC/CG 327 (98.8%) 488 (99.0%) 1.00
AA 13 (3.9%) 18 (3.6%) 0.93 (0.45–1.92) 0.840 GG 4 (1.2%) 5 (1.0%) 0.84 (0.22–3.14) 0.790

 Overdominant CC/AA 288 (87.0%) 379 (76.9%) 1.00 CC/GG 275 (83.1%) 406 (82.4%) 1.00
CA 43 (13.0%) 114 (23.1%) 0.50 (0.34–0.73) <0.001 CG 56 (16.9%) 87 (17.6%) 1.05 (0.73–1.52) 0.790
Allele Allele
C 593 (89.6%) 836 (84.8%) 1.00 C 598 (90.3%) 889 (90.2%) 1.00
A 69 (10.4%) 150 (15.2%) 0.65 (0.48–0.88) 0.005 G 64 (9.7%) 97 (9.8%) 1.02 (0.73–1.42) 0.909

OR: odds ratio; CI: confidence interval; SNP analysis adjusted for age, gender, LVEDD, and LVEF.