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. Author manuscript; available in PMC: 2011 Dec 1.
Published in final edited form as: Arthritis Rheum. 2010 Dec;62(12):3760–3767. doi: 10.1002/art.27742

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).