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Guo J, Zhang T, Cao H, et al. Sequencing of the MHC region defines HLA-DQA1 as the major genetic risk for seropositive rheumatoid arthritis in Han Chinese population. Ann Rheum Dis 2019;78:773–80. doi: 10.1136/annrheumdis-2018-214725.
In the text, all DRβ1:96 hours should be DRβ1:96H.
The sentence on page 775, “followed by DQα1:160A (p=6.25×10−17, OR=2.27, 95% CI 1.87 to 2.75)” should be “followed by DQα1:160A (p=6.25×10−17, OR=0.44, 95% CI 0.36 to 0.53)”.
The sentences on page 776,
“DRβ1:96 hours also showed a significant association (p=6.27×10−7, OR=1.59, 95% CI 1.33 to 1.91)” should be “DRβ1:96H also showed a significant association (p=6.27×10−7, OR=0.64, 95% CI 0.53 to 0.77)”.
“Although DRβ1:96 hours became the second independent signal (p=2.80×10−10, OR=1.68, 95% CI 1.43 to 1.97)” should be “although DRβ1:96H became the second independent signal (p=2.80×10−10, OR=0.58, 95% CI 0.49 to 0.68)”.
“DRβ1:96 hours and DRβ1:37N showed similar independent effects (DRβ1:96 hours: p=4.90×10−16, OR=1.64, 95% CI 1.45 to 1.84…” should be “DRβ1:96H and DRβ1:37N showed similar independent effects (DRβ1:96H: p=4.90×10−16, OR=0.60, 95% CI 0.54 to 0.68…”.
Figure 3 has been corrected. In the revised figure 3, the frequencies on Y axis have been presented according to original frequencies instead of the minor frequencies.
Comparison of individual amino acid frequencies within DQα1:160 and DRβ1:11, 13, 57, 71, and 74 in Han Chinese and European populations. The individual amino acid frequencies are plotted in healthy controls (blue) and cases (red). Upper panel shows the amino acid frequencies in Han Chinese population (the data derived from present study). Lower panel shows the amino acid frequencies in European population (the data cited from Raychaudhur’s study6). (A) DQα1:160D and DQα1:160A are common amino acids in Han Chinese, but the two variants have not been detected in European population. Similar frequencies of amino acids were observed at DRβ1 position 11(B), 13(C), 57(D), 71(E), and 74(F) between Han Chinese and European populations.
Supplementary tables 3–6 and 8 have been corrected. In these tables, a few frequencies have now been presented as original frequencies instead of the minor frequencies and the ORs have been revised accordingly.
Logistic regression analysis in discovery cohort, using gender as covariate
Stepwise conditional analysis on HLA-DQα1:160D in discovery cohort, using gender as covariate
Logistic regression analysis in validation cohort, using gender as covariate
Stepwise conditional analysis on HLA-DQα1:160D in validation cohort, using gender as covariate
Stepwise conditional analysis on HLA-DQα1:160D in combined cohort, using gender as covariate