
@article{ref1,
title="Genetic determinants of both ethanol and acetaldehyde metabolism influence alcohol hypersensitivity and drinking behaviour among Scandinavians",
journal="Clinical and experimental allergy",
year="2010",
author="Linneberg, Allan and Gonzalez-Quintela, A. and Vidal, C. and Jørgensen, T and Fenger, M. and Hansen, Thomas and Pedersen, O. and Husemoen, L. L. N.",
volume="40",
number="1",
pages="123-130",
abstract="Background Although hypersensitivity reactions following intake of alcoholic drinks are common in Caucasians, the underlying mechanisms and clinical significance are not known. In contrast, in Asians, alcohol-induced asthma and flushing have been shown to be because of a single nucleotide polymorphism (SNP), the acetaldehyde dehydrogenase 2 (ALDH2) 487lys, causing decreased acetaldehyde (the metabolite of ethanol) metabolism and high levels of histamine. However, the ALDH2 487lys is absent in Caucasians. Objectives To investigate the genetic determinants of self-reported alcohol-induced hypersensitivity reactions in Caucasians. Methods The study included two population-based studies of 1216 and 6784 adults living in Copenhagen. Assessment of alcohol consumption and hypersensitivity reactions (in a subgroup) was performed by a questionnaire and was related to common SNPs of genes encoding alcohol dehydrogenases (ADHs) and ALDHs. Results In both populations, alcohol drinkers with a genetically determined fast metabolism of ethanol (the A allele of the ADH1b rs1229984) had an increased risk of alcohol-induced hypersensitivity reactions (odds ratio AA/AG vs. GG in combined populations: 1.82, 95% CI 1.04-3.17). In both populations, a common SNP encoding ALDH1b1 (rs2228093) was found to be significantly associated with alcohol-induced hypersensitivity (odds ratio TT vs. CC in combined populations: 2.53, 95% CI 1.31-4.90). Conclusions Our data support that alcohol sensitivity in Caucasians is genetically determined and suggest that a histamine-releasing effect of acetaldehyde represents a plausible biological mechanism. Furthermore, we present the first report of a clinically significant SNP within the acetaldehyde-metabolizing system in a Caucasian population. Cite this as: A. Linneberg, A. Gonzalez-Quintela, C. Vidal, T. Jørgensen, M. Fenger, T. Hansen, O. Pedersen and L. L. N. Husemoen, Clinical & Experimental Allergy, 2010 (40) 123-130.<p /> <p>Language: en</p>",
language="en",
issn="0954-7894",
doi="10.1111/j.1365-2222.2009.03398.x",
url="http://dx.doi.org/10.1111/j.1365-2222.2009.03398.x"
}