Deletion of LCE3C and LCE3B genes at PSORS4 does not contribute to susceptibility to psoriatic arthritis in German patients

被引:32
作者
Hueffmeier, Ulrike [1 ]
Estivill, Xavier [2 ,3 ,4 ]
Riveira-Munoz, Eva [2 ,3 ]
Traupe, Heiko [5 ]
Wendler, Joerg [6 ]
Lohmann, Joerg [7 ]
Boehm, Beate [8 ]
Burkhardt, Harald [8 ]
Reis, Andre [1 ]
机构
[1] Univ Erlangen Nurnberg, Univ Hosp Erlangen, Inst Human Genet, D-91054 Erlangen, Germany
[2] CIBERESP, Ctr Genom Regulat, Barcelona, Spain
[3] CIBERESP, Biomed Res Ctr, Publ Hlth & Epidemiol Network, Barcelona, Spain
[4] Pompeu Fabra Univ, Barcelona, Spain
[5] Univ Munster, Dept Dermatol, D-4400 Munster, Germany
[6] Rheumatol Schwerpunktpraxis, Erlangen, Germany
[7] Psoriasis Rehabil Hosp, Bad Bentheim, Germany
[8] Goethe Univ Frankfurt, Dept Internal Med 2, Div Rheumatol, Frankfurt, Germany
关键词
ASSOCIATION; LOCUS; HLA; FAMILIES; RISK;
D O I
10.1136/ard.2009.108951
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Introduction Psoriasis susceptibility locus 4 (PSORS4) is a susceptibility locus for psoriasis vulgaris (PsV), a common inflammatory, hyperproliferative skin disorder. Recently, a deletion of 2 late cornified envelope (LCE) genes within epidermal differentiation complex on chromosome 1 was shown to be enriched in 1426 patients with PsV, suggesting compromised barrier function in deletion carriers. This genetic association was subsequently confirmed in a German cohort. Methods In order to investigate whether this variant also predisposes to psoriatic arthritis (PsA), this deletion and 3 single nucleotide polymorphisms (SNPs) in strong linkage disequilibrium with it were genotyped in a case-control cohort of 650 patients and 937 control individuals of German origin. Results LCE deletion frequency did not significantly differ between patients with PsA and controls (65.0% vs 65.5%). Similarly, no evidence for association to the three SNPs was observed. Discussion This is the first non-human leucocyte antigen (HLA) risk factor predisposing only to skin type of psoriasis, supporting the concept of partially overlapping but different aetiological factors underlying skin and joint manifestations.
引用
收藏
页码:876 / 878
页数:3
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