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. 2013 Jun 11;8(6):e65657. doi: 10.1371/journal.pone.0065657

Table 5. Genotype and allele frequencies of the SEPS1 G-105A polymorphism in controls and three sub-categories of SPTB neonates.

Cases (%) Controls (%) (n = 673) OR (95% CI) P value
P1 (n = 26) P2 (n = 97) P3 (n = 446) P1 vs. Controls P2 vs. Controls P3 vs. Controls P1 vs. Controls P2 vs. Controls P3 vs. Controls
Genotypes
GG 16 (64.0) 79 (81.4) 363 (81.8) 597 (88.7) Reference Reference Reference Reference Reference Reference
GA 9 (36.0) 18 (18.6) 72 (16.2) 75 (11.1)
AA 0 0 9 (2.0) 1 (0.2)
GA + AA 9 (36.0) 18 (18.6) 81 (18.2) 76 (11.3)
GG vs. GA + AA 4.42 (1.89–10.35)a 1.79 (1.02–3.15)a 1.75 (1.25–2.46)a 0.002a 0.053a 0.001a
GG vs. GA + AA 4.46 (1.86–10.73)b 1.81 (1.03–3.19)b 1.76 (1.25–2.47) b 0.002b 0.050b 0.001b
Alleles
 G allele 0.82 0.91 0.90 0.94 <0.001c 0.054c <0.001c
 A allele 0.18 0.09 0.10 0.06

NOTE: Due to genotyping failure, the actual sample size, respectively, was 566 and 673 for cases and controls. P1, extremely preterm neonates; P2, very preterm neonates; P3, moderately preterm neonates.

Abbreviations: OR, odds ratio; CI, confidence interval.

a

ORs and P values obtained against reference by χ 2 test (2×2).

b

ORs and P values were calculated by multivariate logistic regression, adjusted for maternal age at delivery (year) and neonatal sex.

c

Two-sided χ2 test for distribution of allelic frequencies (df = 1).