A TNF-α promoter polymorphism is associated with juvenile onset psoriasis and psoriatic arthritis

187Citations
Citations of this article
28Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

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; p(corr) < 0.008) with juvenile onset psoriasis and in 20 of 62 patients (32%; p < 0.0003; P(corr) < 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.

Cite

CITATION STYLE

APA

Hohler, T., Kruger, A., Schneider, P. M., Schopf, R. E., Knop, J., Rittner, C., … Marker-Hermann, E. (1997). A TNF-α promoter polymorphism is associated with juvenile onset psoriasis and psoriatic arthritis. Journal of Investigative Dermatology, 109(4), 562–565. https://doi.org/10.1111/1523-1747.ep12337469

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free