Table 2 |
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Association of MICA polymorphism within the second and combined first and second French Caucasian family cohort |
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2nd French family cohort |
1st + 2nd French family cohort |
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(a) All individuals without controlling for LD with HLA-DRB1 |
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Minor allele |
A |
A |
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Frequency in cases/controlsa |
27%/32% |
25%/33% |
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Minor allele transmitted/untransmitted |
37/46 |
63/94 |
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Transmission rate |
45% |
40% |
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TDT P value |
0.328 |
0.015 |
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(b) Subgroup without HLA-DRB1 risk alleles |
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Minor allele transmitted/untransmitted |
12/16 |
18/34 |
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Transmission rate |
43% |
35% |
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TDT P value |
0.450 |
0.027 |
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(c) All individuals, controlling for LD with HLA-DRB1 by conditional logistic regression |
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OR (95% CI)b |
0.68 (0.4–1.15) |
0.56 (0.38–0.83) |
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P value |
0.158 |
0.003 |
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LRTc P value |
0.122 |
0.002 |
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|
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aControls are non-transmitted alleles; bodds ratio of transmission of minor allele versus transmission of major allele as determined in logistic regression; clikelihood ratio test evaluating model including HLA-DRB1 alleles S2 and S3P and MICA-250 versus S2 and S3P only. For the HLA-DRB1 locus, allele L was used as reference. Effects of S2 and S3P alleles are presented in the online supplement (Additional data file 3). CI, confidence interval; LD, linkage disequilibrium; TDT, transmission disequilibrium test. |
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Kirsten et al. Arthritis Research & Therapy 2009 11:R60 doi:10.1186/ar2683 |
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