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. Author manuscript; available in PMC: 2010 Oct 1.
Published in final edited form as: Arthritis Rheum. 2010 Jun;62(6):1712–1717. doi: 10.1002/art.27426

Table 1.

Maternal–offspring HLA–DRB1 compatibility in SLE families compared with paternal–offspring compatibility (father controls) and independent healthy maternal–offspring pairs (healthy controls)*

SLE,
no. (%)
Father controls Healthy controls


HLA–DRB1 compatibility No. (%) OR (95% CI) P No. (%) OR (95% CI) P
Overall
  Unidirectional child-to-parent 96 (13.6) 93 (13.2) 1.01 (0.73–1.41) 0.94 17 (9.0) 1.32 (0.91–2.98) 0.10
  Unidirectional parent-to-child 74 (10.5) 72 (10.2) 1.01 (0.70–1.46) 0.99 22 (11.7) 0.85 (0.56–1.68) 0.89
  Bidirectional 87 (12.3) 99 (14.0) 0.87 (0.62–1.20) 0.38 21 (11.2) 0.65 (0.69–2.08) 0.61
  Not increased 450 (63.6) 443 (62.7) Reference 128 (68.1) Reference
Male and nulligravid female SLE offspring§
  Unidirectional child-to-parent 27 (13.9) 25 (12.9) 0.96 (0.50–1.82) 0.88 17 (9.0) 1.56 (0.78–3.21) 0.19
  Unidirectional parent-to-child 15 (7.7) 19 (9.8) 0.70 (0.31–1.53) 0.36 22 (11.7) 0.67 (0.31–1.43) 0.29
  Bidirectional 22 (11.3) 35 (18.0) 0.56 (0.29–1.04) 0.06 21 (11.2) 1.03 (0.51–2.08) 0.99
  Not increased 130 (67.0) 115 (59.3) Reference 128 (68.1) Reference
*

Histocompatibility was estimated using 2-digit DRB1 typing resolution. SLE = systemic lupus erythematosus; OR = odds ratio; 95% CI = 95% confidence interval.

By Fisher’s exact test.

Comparing 707 maternally affected offspring pairs with 707 paternally affected offspring pairs and 188 independent healthy controls.

§

Comparing 194 maternally affected offspring pairs in which the affected offspring was either a male or a nulligravid female with 194 paternally affected offspring pairs and 188 independent healthy controls.