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. 2014 Feb 20;2014:916202. doi: 10.1155/2014/916202

Table 3.

Genotype and allele frequencies distribution in different sepsis status and healthy controls.

Genotype Healthy control N (%) Sepsis (subtype) N (%) Septic shock N (%) Severe sepsis N (%) P value P value*
P 1 P 2 P 3 P 1* P 2* P 3*
rs2910164
Total 206 34 65 127 0.712 0.888 0.0045 0.712 0.888 0.0045
 CC 101 (49.03) 15 (44.12) 31 (47.69) 42 (33.07)
 GG/GC 105 (50.97) 19 (55.88) 34 (52.31) 85 (66.93)
Allele
 C 295 (71.60) 46 (67.65) 91 (70.00) 153 (60.24)
 G 117 (28.40) 22 (32.35) 39 (30.00) 101 (39.76) 0.564 0.740 0.0029 0.712 0.888 0.0045

rs57095329
Total 205 33 62 127 0.560 0.278 0.413 0.613 0.503 0.421
 AA 135 (65.85) 20 (60.61) 46 (74.19) 78 (61.42)
 GG/GA 70 (34.15) 13 (39.39) 16 (25.81) 49 (38.58)
Allele
 A 334 (81.46) 52 (78.79) 105 (84.68) 200 (78.74)
 G 76 (18.54) 14 (21.21) 19 (15.32) 54 (21.26) 0.613 0.503 0.421 0.613 0.503 0.421

OR: odds ratio; 95% CI: 95% confidence interval. *False discovery rate-adjusted P value for multiple hypotheses testing using the Benjamini-Hochberg method. P 1 and P 1*: healthy control group versus sepsis group. P 2 and P 2*: healthy control group versus septic shock group. P 3 and P 3*: healthy control group versus severe sepsis group. Fisher's exact test P 3 = 0.0045, OR = 1.947, 95% CI (1.229–3.083) for genotype in rs2910164; P 3 = 0.0029, OR = 1.664, 95% CI (1.196–2.316) for allele in rs2910164.