Evaluation of interleukin 13 polymorphisms in systemic sclerosis View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2006-08

AUTHORS

Brigitte Granel, Christophe Chevillard, Yannick Allanore, Violaine Arnaud, Sandrine Cabantous, Sandrine Marquet, Pierre-Jean Weiller, Jean-Marc Durand, Jean-Robert Harlé, Claire Grange, Yves Frances, Philippe Berbis, Jean Gaudart, Philippe de Micco, André Kahan, Alain Dessein

ABSTRACT

Systemic sclerosis (SSc) is a multisystem disease of unknown etiology. It is characterized by excessive cutaneous and visceral fibrosis, damage to small blood vessels, and production of autoantibodies. Interleukin-13 (IL-13) has been shown to be involved in abnormal fibrosis in other diseases. Therefore, we have evaluated its possible involvement in SSc. We analyzed four IL13 gene polymorphisms, rs1800925 (IL13-1055), rs20541 (Arg130Gln), rs847, and rs2243204 in 107 unrelated SSc patients (40 patients having diffuse cutaneous form and 67 patients having limited cutaneous form) and in 170 controls. All subjects were Caucasians. In the total patient population and in the diffuse cutaneous subset, we observed an association between two IL13 polymorphisms, IL13 rs1800925 (IL13-1055), and IL13 rs2243204, and disease (p=0.03-0.04). The IL13 rs2243204T allele was more common in SSc patients (p=0.01, OR=2.3 CI 1.21-4.38) and in the diffuse cutaneous form (p=0.01, OR=2.95, CI 1.35-6.49) than in control subjects. Our result supports the suggestion that polymorphisms in IL13 are associated to SSc and skin fibrosis process. However, further studies on larger and independent population and functional analyses are needed to confirm these findings. More... »

PAGES

693-699

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00251-006-0135-0

DOI

http://dx.doi.org/10.1007/s00251-006-0135-0

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1027381089

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/16832637


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