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. 2012 Aug 8;12:41. doi: 10.1186/1471-2466-12-41

Table 3.

Association ofACEgene D/I polymorphism with onset of clinical symptoms of patients in months considering the cohorts toCFTRmutation

Groups ACEgenotype ≤ 3 months > 3 months Total X2 p X2 p OR (CI 5-95%)
Without taking CFTR mutation into account
I/I
38
28
66
0,880
0,644
0.012
0.9136
1.035 (0.555 - 1.931)
I/D
44
37
81
0.473
0.492
0.808 (0.4396 -1.484)
D/D
15
8
23
0.723
0.395
1.486 (0.5937, 3.721)
No identified CFTR mutation
I/I
13
6
19
1,685
0,431
0.825
0.364
1.806 (0.5017 -6.498)
I/D
9
9
18
1.624
0.203
0.438 (0.122 - 1.576)
D/D
3
1
4
0.357
0.977
2.045 (0.194 - 21.58)
One CFTR mutation identified class I, II or III
I/I
10
11
21
5,564
0,062
4.217
0.049
0.297 (0.084 – 0.995)
I/D
14
6
20
0.521
0.471
1.167 (0.775 – 1.757)
D/D
8
1
9
2.951
0.097
5,667 (0,647 – 49,61)
Two CFTR mutation identified class I, II and/or III I/I
15
11
26
0,599 1,026 0.773
0.379
1.527 (0.593 - 3.936)
I/D
21
22
43
0.122
0.727
0.854 (0.352 - 2.072)
D/D 4 6 10 0.511 0.704 0.611 (0.158 - 2.358)

Values below 0.05 for p denote clinical correlation between variables. OR - odds ratio, CI- confidence interval, ≤ − less than or equal to, > − greater, D - deleted allele, I - insertion allele. No identified mutation (44 patients) – patients without of identified mutation in classes I, II or III. One identified mutation (51 patients) – patient with one identified mutation in class I, II, or III. Two identified mutation (85 patients) – patient with two mutations in class I, II or III.