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Association of systemic lupus erythematosus clinical features with European population genetic substructure
Authors:Alonso-Perez Elisa,Suarez-Gestal Marian,Calaza Manuel,Witte Torsten,Papasteriades Chryssa,Marchini Maurizio,Migliaresi Sergio,Kovacs Attila,Ordi-Ros Josep,Bijl Marc,Santos Maria Jose,Ruzickova Sarka,Pullmann Rudolf,Carreira Patricia,Skopouli Fotini N,D'Alfonso Sandra,Sebastiani Gian Domenico,Suarez Ana,Blanco Francisco J,Gomez-Reino Juan J,Gonzalez Antonio  European Consortium of SLE DNA Collections
Affiliation:Laboratorio de Investigacion, Instituto de Investigacion Sanitaria, Universitario de Santiago Hospital Clinico Santiago de Compostela, Santiago de Compostela, Spain.
Abstract: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.
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