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. 2015 Sep 21;21:2809–2827. doi: 10.12659/MSM.894273

Supplementary Table 13.

Distribution of genotypes of the 46438521G>C – NEIL1, c.2285T>C – PARP-1, c.–1370T>A – POLG, c.580C>T – XRCC1 and c.1196A>G – XRCC1 polymorphisms in patients with undefined form of Fuchs dystrophy and controls.

Polymorphism genotype/allele Controls FECD Crude OR (95% CI) p Adjusted OR* (95% CI) p
Number (frequency)
g.46438521G>C NEIL1
 C/C 98 (0.28) 6 (0.22) 0.61 (0.20–1.83) 0.379 0.61 (0.20–1.83) 0.379
 C/G 240 (0.68) 20 (0.74) 1.34 (0.55–3.27) 0.513 1.66 (0.60–4.62) 0.331
 G/G 15 (0.04) 1 (0.04) 0.86 (0.11–6.82) 0.892 0.73 (0.08–6.34) 0.773
 C 436 (0.62) 32 (0.59) 0.82 (0.38–1.79) 0.625 0.76 (0.32–1.79) 0.532
 G 270 (0.38) 22 (0.41) 1.21 (0.56–2.63) 0.625 0.31 (0.56–3.07) 0.532
c.2285T>C PARP-1
 A/A 239 (0.68) 22 (0.81) 2.10 (0.77–5.68) 0.145 2.65 (0.85–8.30) 0.093
 A/G 114 (0.32) 5 (0.19) 0.48 (0.18–1.29) 0.145 0.38 (0.12–1.18) 0.093
 G/G 0 (0.00) 0 (0.00)
 A 592 (0.84) 49 (0.91) 2.10 (0.77–5.68) 0.145 2.65 (0.85–8.30) 0.093
 G 114 (0.16) 5 (0.09) 0.48 (0.18–1.29) 0.145 0.38 (0.12–1.18) 0.093
c.–1370T>A POLG
 A/A 46 (0.13) 6 (0.22) 1.91 (0.73–4.97) 0.187 1.63 (0.544–4.88) 0.382
 A/T 203 (0.57) 14 (0.52) 0.80 (0.36–1.74) 0.568 1.34 (0.55–3.29) 0.519
 T/T 104 (0.30) 7 (0.26) 0.84 (0.34–2.04) 0.697 0.47 (0.16–1.40) 0.178
 A 295 (0.42) 26 (0.48) 1.37 (0.74–2.52) 0.318 1.61 (0.83–3.13) 0.156
 T 411 (0.58) 28 (0.52) 0.62 (0.32–1.20) 0.156 0.62 (0.32–1.20) 0.156
c.580C>T XRCC1
 C/C 305 (0.86) 25 (0.93) 1.97 (0.45–8.57) 0.368 1.38 (0.29–6.43) 0.678
 C/T 48 (0.14) 2 (0.07) 0.51 (0.12–2.21) 0.368 0.72 (0.15–3.36) 0.678
 T/T 0 (0.00) 0 (0.00)
 C 653 (0.92) 52 (0.96) 2.21 (0.51–9.60) 0.291 1.40 (0.30–6.49) 0.668
 T 53 (0.08) 2 (0.04) 0.45 (0.10–1.97) 0.291 0.71 (0.15–3.31) 0.668
c.1196A>G XRCC1
 A/A 72 (0.20) 10 (0.37) 2.30 (1.01–5.23) 0.048 2.16 (1.16–7.26) 0.022
 A/G 218 (0.62) 15 (0.56) 0.77 (0.35 0 1.70) 0.525 0.58 (0.24–1.41) 0.228
 G/G 63 (0.18) 2 (0.07) 0.39 (0.08–1.59) 0.182 0.29 (0.03–2.25) 0.235
 A 362 (0.51) 35 (0.65) 2.06 (1.07–3.96) 0.030 2.58 (1.18–5.67) 0.018
 G 344 (0.49) 19 (0.35) 0.49 (0.25–0.93) 0.030 0.39 (0.18–0.85) 0.018

p values <0.05 along with corresponding ORs are in bold;

*

OR adjusted for co-occurrence of visual impairment, sex, age and family history for FECD.