1. A variant of theCXCL11gene may influence susceptibility to contact allergy, particularly in polysensitized patients
- Author
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Thomas Brüning, Thomas Werfel, Kristian Reich, Claudia Schröder-Kraft, Götz A. Westphal, Sibylle Schliemann, Harald Löffler, Christiane Szliska, Elke Weisshaar, Heinrich Dickel, Claudia Pföhler, Andrea Bauer, Hilmar Schwantes, Sonja Molin, Burkhard Kreft, Kristine Breuer, Axel Schnuch, Knut Schäkel, Hans-Peter Rihs, Johannes Geier, Margitta Worm, Richard Brans, Thomas Zeiler, Jürgen Bünger, Annice Heratizadeh, and Antje Schaffranek
- Subjects
0301 basic medicine ,Patch test ,Dermatology ,Odds ratio ,Biology ,3. Good health ,030207 dermatology & venereal diseases ,03 medical and health sciences ,030104 developmental biology ,0302 clinical medicine ,Increased risk ,Contact allergy ,Genotype ,Multiple comparisons problem ,Immunology ,Immunology and Allergy ,CXCL11 ,Gene - Abstract
Summary Background Hereditary factors may influence individual susceptibility to contact allergy (CA). Objectives To investigate genetic variants with impacts on early inflammatory reactions and T cell functions that possibly increase the risk of CA. Patients and Methods Three hundred and seventy two patients undergoing patch testing were recruited from the Information Network of Departments of Dermatology (IVDK). Of these, 133 were monosensitized and 239 were polysensitized, defined as reacting to three or more unrelated sensitizers. Within the polysensitized individuals, a subgroup with at least one particularly strong patch test reaction (strong reactors; n = 194) was considered. Three hundred and forty-seven blood bank donors served as controls. Fifteen genetic variants in 13 genes were analysed. Results The homozygous variant CXCL11 AA genotype (rs6817952) was significantly more frequent among polysensitized patients (10 of 239 = 4.2%; p = 0.0048; odds ratio 7.49; 95%CI: 1.7–36.1) than among monosensitized patients (2.2%) and in the control group (0.6%). None of the remaining genetic variants investigated were characterized by similarly strong associations. However, the significance was lost after correction for multiple comparisons. Conclusions The homozygous variant CXCL11 genotype is associated with an increased risk of CA. To confirm this exploratory finding, further independent studies are needed.
- Published
- 2016
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