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Publikationsserver der RWTH Aachen University

Fall-Kontrollstudie zur Bedeutung von Polymorphismen im MnSOD-Gen für die Sensibilisierung auf para-Phenylendiamin (PPD)

Abstract

dc:description

Allergic contact dermatitis is a hypersensitivity reaction of the skin which is caused by a combination of environmental factors and individual susceptibility. The reason why one individual develops an allergic contact dermatitis whereas others are not affected even under long term allergen exposure is not completely understood. The dye para-phenylene diamine (PPD) is a very common and potent contact sensitizer in man. It has been found that oxidative stress from reactive oxygen species (ROS) may play an important role in the pre-immunological phase of allergic contact dermatitis to PPD. Manganese superoxide dismutase (MnSOD) is one of the primary enzymes that directly scavenge potential harmful oxidizing species. Several genetic polymorphisms in the MnSOD gene have been associated with various disease risks. A single nucleotide exchange from cytosine to thymine at position 47 in the mitochondrial targeting sequence in exon 2 results in an amino acid exchange at position -9 in the signal peptide from alanin to valine (Ala-9Val). The same nucleotide exchange at nucleotide position 339 in exon 3 results in an amino acid exchange at position 58 from threonine to isoleucin (Ile58Thr). The aim of this case-control study was to establish suitable methods for detection of polymorphisms Ala-9Val and Ile58Thr and to investigate their possible association with contact sensitization to PPD in humans.The study was performed in 165 unrelated Caucasian cases and 202 age- and gender matched Caucasian controls. As no heterozygous (CT) or homozygous carrier (CC) for Ile58Thr was found, an association of this polymorphism with contact sensitization to PPD can be excluded. For Ala-9Val no statistically significant differences for genotypes and allelic frequencies between cases and controls (p > 0.05) were detected. However, there was an increased number of persons homozygous for the cytosine allele (Ala) among cases (27.4% vs. 22.9%, OR = 1.3). This was especially evident for female cases (28.9% vs. 22.9%, OR = 1.3), subjects older than 45 years (26.4% vs. 21.0%, OR = 1.3) and female cases older than 45 years (24.5% vs. 17.9%, OR = 1.5). Although this polymorphism apparently has no strong impact on the individual susceptibility to develop a sensitization to PPD, these results may show an increased risk for females, especially of higher age.

Degree

thesis:*
Grantor dc:publisher
Publikationsserver der RWTH Aachen University
Year dc:date
2005

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Brans, Richard
Contributors dc:contributor
  • Blömeke, Brunhilde

Subjects

dc:subject × 12

Rights

dc:rights
Statement dc:rights
  • info:eu-repo/semantics/openAccess
Language dc:language
ger

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:publications.rwth-aachen.de:62205

Chain of custody

source
Harvested from
RWTH Aachen University
Base URL
publications.rwth-aachen.de/oai2d
Last updated
2026-07-30
Source record
OAI-PMH GetRecord
citation

Brans, Richard. Fall-Kontrollstudie zur Bedeutung von Polymorphismen im MnSOD-Gen für die Sensibilisierung auf para-Phenylendiamin (PPD). Publikationsserver der RWTH Aachen University, 2005. https://publications.rwth-aachen.de/record/62205