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RESEARCH PRODUCT

A TNF-α Promoter Polymorphism Is Associated with Juvenile Onset Psoriasis and Psoriatic Arthritis

Karl-h. Meyer Zum BüschenfeldePeter M. SchneiderJürgen KnopRudolfe E. SchopfThomas HöhlerElisabeth Märker-hermannChristian RittnerAnke Kruger

subject

ArthritisCell BiologyDermatologyHuman leukocyte antigenBiologymedicine.diseaseMajor histocompatibility complexBiochemistrycytokinesmajor histocompatibility complexPathogenesisPsoriatic arthritisPsoriasisImmunologymedicinebiology.proteinTumor necrosis factor alphaHLA antigensAge of onsetMolecular Biologylinkage disequilibrium

description

Tumor necrosis factor-α is considered to be one of the important mediators in the pathogenesis of psoriasis. A strong association of juvenile onset psoriasis with the major histocompatibility complex encoded HLA-Cw6 antigen has been reported but it is unclear whether Cw6 itself or a closely linked gene is involved in the pathogenesis. This study has focused on the association of promoter polymorphisms of the major histocompatibility complex encoded tumor necrosis factor-α gene with psoriasis and psoriatic arthritis. Tumor necrosis factor-α promoter polymorphisms were sought by sequence-specific oligonucleotide hybridization and by direct sequencing in Caucasian patients with juvenile onset psoriasis and with psoriatic arthritis and in healthy controls. A mutation at position −238 of the tumor necrosis factor-α promoter was present in 23 of 60 patients (38%; p < 0.0001; Pcorr < 0.008) with juvenile onset psoriasis and in 20 of 62 patients (32%; p < 0.0003; Pcorr < 0.03) with psoriatic arthritis, compared with seven of 99 (7%) Caucasian controls. There was a marked increase of homozygotes for this mutation in the psoriasis group. Another mutation at position −308 was found in similar proportions of patients and controls. Our study shows a strong association of the tumor necrosis factor-α promoter polymorphism at position −238 with psoriasis and psoriatic arthritis. Our findings suggest that this promoter polymorphism itself or a gene in linkage disequilibrium with tumor necrosis factor-α predispose to the development of psoriasis.

https://doi.org/10.1111/1523-1747.ep12337469