Table 1.
HLA Alleles | SS ~ HLA | SSA ~ HLA | epigIFN ~ HLA | epigIFN ~ HLA + SSA | SS ~ HLA (positive epigIFN) | SS ~ HLA (negative epigIFN) | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
beta.HLA | P.HLA | beta.HLA | P.HLA | beta.HLA | P.HLA | beta.HLA | P.HLA | beta.HLA | P.HLA | beta.HLA | P.HLA | |
DRB1_0301 | 1.14 | 2.07E-07 | 0.27 | 1.02 x 10–04 | − 0.17 | 9.16 x 10–05 | − 0.06 | 0.142 | 1.40 | 7.14 x 10–09 | − 0.30 | 0.470 |
DQB1_0201 | 1.16 | 1.39E-07 | 0.29 | 2.03 x 10–05 | − 0.18 | 6.55 x 10–05 | − 0.05 | 0.210 | 1.44 | 2.58 x 10–09 | − 0.29 | 0.493 |
β reflects the additive effect of allele dosage for different HLA alleles and P is the associated significance level. The association between HLA genetic variation, SS and SSA was determined by means of logistic regression adjusted by sex and age. The association between HLA genetic variation and epigIFN was determined by linear regression models adjusted by sex, age, cell proportions and batch effects.
epigIFN refers to the epigenetic IFN signature. DNA methylation at IFI44L gene (cg13452062) was used as a proxy for epigIFN. Patients exhibiting DNAm > 0.8 were classified as negative epigIFN. Patients exhibiting DNAm < 0.8 were classified as positive epigIFN.