Table 2.
Results of Z and/or S allele carriage determining α1AT deficiency (under a codominant model) and association with WG*
Genotype | Cases, no. (%) | Controls, no. (%) | OR (95% CI) | P |
---|---|---|---|---|
All genotypes | ||||
MM | 353 (81.5) | 371 (88.1) | 1 (reference) | – |
MS and MZ | 70 (16.2) | 50 (11.9) | 1.47 (0.98–2.22) | 0.06 |
SS, ZZ, and SZ | 10 (2.3) | 0 (0) | 14.58 (2.33–∞) | 0.002 |
S genotypes excluded | ||||
MM | 353 (92.2) | 371 (95.4) | 1 (reference) | – |
MZ | 26 (6.8) | 18 (4.6) | 1.52 (0.79–2.99) | 0.24 |
ZZ | 4 (1.0) | 0 (0) | 5.53 (0.69–∞) | 0.11 |
Z genotypes excluded | ||||
MM | 353 (88.0) | 371 (92.1) | 1 (reference) | – |
MS | 44 (11.0) | 32 (7.9) | 1.44 (0.87–2.41) | 0.16 |
SS | 4 (1.0) | 0 (0) | 5.53 (0.69–∞) | 0.11 |
OR = odds ratio; 95% CI = 95% confidence interval (see Table 1 for other definitions).