PLoS ONE (Jan 2011)

Association of systemic lupus erythematosus clinical features with European population genetic substructure.

  • Elisa Alonso-Perez,
  • Marian Suarez-Gestal,
  • Manuel Calaza,
  • Torsten Witte,
  • Chryssa Papasteriades,
  • Maurizio Marchini,
  • Sergio Migliaresi,
  • Attila Kovacs,
  • Josep Ordi-Ros,
  • Marc Bijl,
  • Maria Jose Santos,
  • Sarka Ruzickova,
  • Rudolf Pullmann,
  • Patricia Carreira,
  • Fotini N Skopouli,
  • Sandra D'Alfonso,
  • Gian Domenico Sebastiani,
  • Ana Suarez,
  • Francisco J Blanco,
  • Juan J Gomez-Reino,
  • Antonio Gonzalez,
  • European Consortium of SLE DNA Collections

DOI
https://doi.org/10.1371/journal.pone.0029033
Journal volume & issue
Vol. 6, no. 12
p. e29033

Abstract

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Systemic Lupus Erythematosus (SLE) is an autoimmune disease with a very varied spectrum of clinical manifestations that could be partly determined by genetic factors. We aimed to determine the relationship between prevalence of 11 clinical features and age of disease onset with European population genetic substructure. Data from 1413 patients of European ancestry recruited in nine countries was tested for association with genotypes of top ancestry informative markers. This analysis was done with logistic regression between phenotypes and genotypes or principal components extracted from them. We used a genetic additive model and adjusted for gender and disease duration. Three clinical features showed association with ancestry informative markers: autoantibody production defined as immunologic disorder (P = 6.8×10(-4)), oral ulcers (P = 6.9×10(-4)) and photosensitivity (P = 0.002). Immunologic disorder was associated with genotypes more common in Southern European ancestries, whereas the opposite trend was observed for photosensitivity. Oral ulcers were specifically more common in patients of Spanish and Portuguese self-reported ancestry. These results should be taken into account in future research and suggest new hypotheses and possible underlying mechanisms to be investigated. A first hypothesis linking photosensitivity with variation in skin pigmentation is suggested.