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The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population

Alcohol intake affects in great the symptoms and life of  psoriasis patients, although the association of SNPs related to increased alcohol consumption with psoriasis has not been elucidated. Therefore, to investigate the association of psoriasis with established alcohol consumption and dependence-r...

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Autores principales: Szentkereszty-Kovács, Zita, Fiatal, Szilvia, Szegedi, Andrea, Kovács, Dóra, Janka, Eszter, Herszényi, Krisztina, Holló, Péter, Nikamo, Pernilla, Ståhle, Mona, Remenyik, Éva, Törőcsik, Dániel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594982/
https://www.ncbi.nlm.nih.gov/pubmed/31011876
http://dx.doi.org/10.1007/s00403-019-01915-y
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author Szentkereszty-Kovács, Zita
Fiatal, Szilvia
Szegedi, Andrea
Kovács, Dóra
Janka, Eszter
Herszényi, Krisztina
Holló, Péter
Nikamo, Pernilla
Ståhle, Mona
Remenyik, Éva
Törőcsik, Dániel
author_facet Szentkereszty-Kovács, Zita
Fiatal, Szilvia
Szegedi, Andrea
Kovács, Dóra
Janka, Eszter
Herszényi, Krisztina
Holló, Péter
Nikamo, Pernilla
Ståhle, Mona
Remenyik, Éva
Törőcsik, Dániel
author_sort Szentkereszty-Kovács, Zita
collection PubMed
description Alcohol intake affects in great the symptoms and life of  psoriasis patients, although the association of SNPs related to increased alcohol consumption with psoriasis has not been elucidated. Therefore, to investigate the association of psoriasis with established alcohol consumption and dependence-related gene variants we conducted a population-based case–control study including 3743 subjects (776 psoriasis cases and 2967 controls from the general Hungarian population). Genotyping of 23 SNPs at ADH1B, ADH1C, ALDH1A1, ALDH2, SLC6A3, DDC, GABRA2, GABRG1, HTR1B, MAOA, TPH2, CHRM2, GRIN2A, POMC, OPRM1, OPRK1 and BDNF were determined and differences in genotype and allele distributions were investigated. Multiple logistic regression analyses were implemented. Analysis revealed association between C allele of the rs1229984 polymorphism (ADH1B gene) and psoriasis risk (OR(additive) = 1.58, 95% CI 1.23–2.03, p < 0.001, OR(recessive) = 1.58, 95% CI 1.22–2.04, p = 0.001). Furthermore, the G allele of rs1799971 polymorphism (OPRM1 gene) increased the risk of familial aggregation (OR(additive) = 1.99, 95% CI 1.36–2.91, p < 0.001 OR(dominant) = 2.01, 95% CI 1.35–3.01, p < 0.001). In subgroups of psoriatic patients with history of early onset and familial aggregation effect allele ‘C’ of rs1229984 showed association in the additive and recessive models (OR(additive) = 2.41, 95% CI 1.26–4.61, p < 0.01, OR(recessive) = 2.42, 95% CI 1.26–4.68, p < 0.01). While effect allele ‘G’ of rs1799971 (OPRM1) also associated with increased risk of early onset and familial aggregation of psoriasis in the additive and dominant models (OR(additive) = 1.75, 95% CI 1.27–2.43, p = 0.001, OR(dominant) = 1.82, 95% CI 1.26–2.63, p = 0.001). Our results suggest that genetically defined high-risk individuals for alcohol consumption are more common in the psoriasis population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00403-019-01915-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-65949822019-07-11 The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population Szentkereszty-Kovács, Zita Fiatal, Szilvia Szegedi, Andrea Kovács, Dóra Janka, Eszter Herszényi, Krisztina Holló, Péter Nikamo, Pernilla Ståhle, Mona Remenyik, Éva Törőcsik, Dániel Arch Dermatol Res Original Paper Alcohol intake affects in great the symptoms and life of  psoriasis patients, although the association of SNPs related to increased alcohol consumption with psoriasis has not been elucidated. Therefore, to investigate the association of psoriasis with established alcohol consumption and dependence-related gene variants we conducted a population-based case–control study including 3743 subjects (776 psoriasis cases and 2967 controls from the general Hungarian population). Genotyping of 23 SNPs at ADH1B, ADH1C, ALDH1A1, ALDH2, SLC6A3, DDC, GABRA2, GABRG1, HTR1B, MAOA, TPH2, CHRM2, GRIN2A, POMC, OPRM1, OPRK1 and BDNF were determined and differences in genotype and allele distributions were investigated. Multiple logistic regression analyses were implemented. Analysis revealed association between C allele of the rs1229984 polymorphism (ADH1B gene) and psoriasis risk (OR(additive) = 1.58, 95% CI 1.23–2.03, p < 0.001, OR(recessive) = 1.58, 95% CI 1.22–2.04, p = 0.001). Furthermore, the G allele of rs1799971 polymorphism (OPRM1 gene) increased the risk of familial aggregation (OR(additive) = 1.99, 95% CI 1.36–2.91, p < 0.001 OR(dominant) = 2.01, 95% CI 1.35–3.01, p < 0.001). In subgroups of psoriatic patients with history of early onset and familial aggregation effect allele ‘C’ of rs1229984 showed association in the additive and recessive models (OR(additive) = 2.41, 95% CI 1.26–4.61, p < 0.01, OR(recessive) = 2.42, 95% CI 1.26–4.68, p < 0.01). While effect allele ‘G’ of rs1799971 (OPRM1) also associated with increased risk of early onset and familial aggregation of psoriasis in the additive and dominant models (OR(additive) = 1.75, 95% CI 1.27–2.43, p = 0.001, OR(dominant) = 1.82, 95% CI 1.26–2.63, p = 0.001). Our results suggest that genetically defined high-risk individuals for alcohol consumption are more common in the psoriasis population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00403-019-01915-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-04-22 2019 /pmc/articles/PMC6594982/ /pubmed/31011876 http://dx.doi.org/10.1007/s00403-019-01915-y Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Szentkereszty-Kovács, Zita
Fiatal, Szilvia
Szegedi, Andrea
Kovács, Dóra
Janka, Eszter
Herszényi, Krisztina
Holló, Péter
Nikamo, Pernilla
Ståhle, Mona
Remenyik, Éva
Törőcsik, Dániel
The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population
title The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population
title_full The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population
title_fullStr The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population
title_full_unstemmed The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population
title_short The prevalence of ADH1B and OPRM1 alleles predisposing for alcohol consumption are increased in the Hungarian psoriasis population
title_sort prevalence of adh1b and oprm1 alleles predisposing for alcohol consumption are increased in the hungarian psoriasis population
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594982/
https://www.ncbi.nlm.nih.gov/pubmed/31011876
http://dx.doi.org/10.1007/s00403-019-01915-y
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