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. 2016 Mar 10;11(3):e0149441. doi: 10.1371/journal.pone.0149441

Table 1. Association studies for CTLA4 gene exon 1 +49A/G and 3’UTR CT60A/G polymorphisms and TG gene exon 33 polymorphism in autoimmune hypothyroidism patients.

SNP Genotype or allele Patients (Frequency) n = 49 Controls (Frequency) n = 62 P for Association Odds ratio (95% CI)
CTLA4 Exon1 (+49A/G) AA 8(0.16) 32(0.52) R 1
AG 28(0.57) 21(0.34) 0.0004a 5.333(2.043 to 13.92)
GG 13(0.27) 9(0.14) 0.0019b 5.778(1.829 to 18.25)
A 44(0.45) 85(0.69) 0.0004c
G 54(0.55) 39(0.31)
CTLA4 (CT60A/G) 3’UTR AA 4(0.08) 22(0.35) R 1
AG 15(0.31) 17(0.27) 0.0110a 4.853(1.360 to 17.31)
GG 30(0.61) 23(0.37) 0.0005b 7.174(2.169 to 23.73)
A 23(0.23) 61(0.49) <0.0001c
G 75(0.77) 63(0.51)
TG Exon33 TT 4(0.08) 29(0.47) R 1
TC 28(0.57) 27(0.43) 0.0003a 7.519(2.329 to 24.27)
CC 17(0.35) 6(0.10) < 0.0001b 20.54(5.065 to 83.30)
T 36(0.37) 85(0.69) <0.0001c
C 62(0.63) 39(0.31)

‘n’ represents number of Patients/ Controls, CI refers to Confidence Interval, R refers to Reference Group

a and b represents Patients vs. Controls (genotype) using chi-squared test with 2 × 2 contingency table for AA vs AG and AA vs GG of +49A/G and CT60, and respectively for TT vs CT and TT vs CC of TG exon33.

c represents Patients vs. Controls (allele) using chi-squared test with 2 × 2 contingency table.