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Gewählte Publikation:

Schnuch, A; Westphal, GA; Müller, MM; Schulz, TG; Geier, J; Brasch, J; Merk, HF; Kawakubo, Y; Richter, G; Koch, P; Fuchs, T; Gutgesell, T; Reich, K; Gebhardt, M; Becker, D; Grabbe, J; Szliska, C; Aberer, W; Hallier, E.
Genotype and phenotype of N-acetyltransferase 2 (NAT2) polymorphism in patients with contact allergy.
Contact Dermatitis. 1998; 38(4):209-211 Doi: 10.1111/j.1600-0536.1998.tb05709.x
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Co-Autor*innen der Med Uni Graz
Aberer Werner
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Abstract:
We investigated whether patients with contact allergy differed from non-contact-allergic, non-atopic controls with regard to genotype and phenotype of the polymorphic enzyme N-acetyltransferase 2 (NAT2). 55 contact-allergic patients recruited from the Information Network of Departments of Dermatology (IVDK) were compared to 85 controls from among local health care personnel. NAT2 activity was calculated from HPLC analysis of the ratio of the caffeine metabolites 5-acetylamino-6-formylamino-3-methyluracil (AFMU) and 1-methylxanthine (1MX) in the urine. NAT2 genotype was determined by polymerase chain reaction (PCR). A statistically significantly increased proportion of rapid acetylators was found in contact-allergic patients. This may have 2 possible implications: acetylation may enhance contact sensitization; or NAT2 status may be a genetic marker for contact sensitizability.
Find related publications in this database (using NLM MeSH Indexing)
Acetylation -
Arylamine N-Acetyltransferase - genetics Arylamine N-Acetyltransferase - metabolism
Caffeine - blood Caffeine - urine
Chromatography, High Pressure Liquid -
Dermatitis, Allergic Contact - enzymology Dermatitis, Allergic Contact - genetics
Genotype -
Humans -
Phenotype -
Phosphodiesterase Inhibitors - blood Phosphodiesterase Inhibitors - urine
Polymerase Chain Reaction -
Polymorphism, Restriction Fragment Length -
Sulfamethazine - metabolism

Find related publications in this database (Keywords)
aryl amines
acetylator phenotype
acetylator genotype
allergic contact dermatitis
genetic susceptibility
molecular epidemiology
clinical epidemiology
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