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21 September 2015 : Laboratory Research  

Variation in DNA Base Excision Repair Genes in Fuchs Endothelial Corneal Dystrophy

Katarzyna A. Wójcik BCDEF , Ewelina Synowiec BCDF , Piotr Polakowski D , Janusz Błasiak AEF , Jerzy Szaflik AFG , Jacek P. Szaflik AEG

DOI: 10.12659/MSM.894273

Med Sci Monit 2015; 21:2809-2827

Supplementary Table 1. Distribution of combined genotypes of the g.46438521G>C – NEIL1 and c.2285T>C – PARP-1 polymorphisms and odds ratio (OR) with 95% confidence interval (95% CI) in patients with Fuchs endothelial corneal dystrophy (FECD) and controls.

Combined genotypesControls (n=353)FECD (n=250)Crude OR (95% CI)pAdjusted OR* (95% CI)p
Number (frequency)
C/C – A/A64 (0.18)35 (0.14)0.73 (0.47–1.15)0.1780.90 (0.53–1.53)0.702
C/C – A/G34 (0.10)18 (0.07)0.73 (0.40–1.32)0.296
C/C – G/G0 (0.00)0 (0.00)
C/G – A/A167 (0.47)126 (0.50)1.13 (0.82–1.56)0.4541.11 (0.76–1.62)0.595
C/G – A/G73 (0.21)62 (0.25)1.26 (0.86–1.86)0.2321.42 (0.91–2.25)0.122
C/G – G/G0 (0.00)0 (0.00)
G/G – A/A8 (0.02)5 (0.02)0.88 (0.28–2.73)0.8251.38 (0.90–2.11)0.924
G/G – A/G7 (0.02)4 (0.02)0.80 (0.23–2.77)0.7300.53 (0.13–2.15)0.376
G/G – G/G0 (0.00)0 (0.00)
values
* OR adjusted for co-occurrence of visual impairment, sex, age and family history for FECD.

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Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750