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Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases

BACKGROUND: The majority of non-syndromic colorectal cancers (CRCs) can be described as a complex disease. A two-stage case–control study on CRC susceptibility was conducted to assess the influence of the ancestral alleles in the polymorphisms previously associated with nutrition-related complex dis...

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Autores principales: Huhn, Stefanie, Bevier, Melanie, Rudolph, Anja, Pardini, Barbara, Naccarati, Alessio, Hoffmeister, Michael, Vodickova, Ludmila, Novotny, Jan, Brenner, Hermann, Chang-Claude, Jenny, Hemminki, Kari, Vodicka, Pavel, Försti, Asta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522999/
https://www.ncbi.nlm.nih.gov/pubmed/23036011
http://dx.doi.org/10.1186/1471-2350-13-94
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author Huhn, Stefanie
Bevier, Melanie
Rudolph, Anja
Pardini, Barbara
Naccarati, Alessio
Hoffmeister, Michael
Vodickova, Ludmila
Novotny, Jan
Brenner, Hermann
Chang-Claude, Jenny
Hemminki, Kari
Vodicka, Pavel
Försti, Asta
author_facet Huhn, Stefanie
Bevier, Melanie
Rudolph, Anja
Pardini, Barbara
Naccarati, Alessio
Hoffmeister, Michael
Vodickova, Ludmila
Novotny, Jan
Brenner, Hermann
Chang-Claude, Jenny
Hemminki, Kari
Vodicka, Pavel
Försti, Asta
author_sort Huhn, Stefanie
collection PubMed
description BACKGROUND: The majority of non-syndromic colorectal cancers (CRCs) can be described as a complex disease. A two-stage case–control study on CRC susceptibility was conducted to assess the influence of the ancestral alleles in the polymorphisms previously associated with nutrition-related complex diseases. METHODS: In stage I, 28 single nucleotide polymorphisms (SNPs) were genotyped in a hospital-based Czech population (1025 CRC cases, 787 controls) using an allele-specific PCR-based genotyping system (KASPar®). In stage II, replication was carried out for the five SNPs with the lowest p values. The replication set consisted of 1798 CRC cases and 1810 controls from a population-based German study (DACHS). Odds ratios (ORs) and 95% confidence intervals (CIs) for associations between genotypes and CRC risk were estimated using logistic regression. To identify signatures of selection, Fay-Wu’s H and Integrated Haplotype Score (iHS) were estimated. RESULTS: In the Czech population, carriers of the ancestral alleles of AGT rs699 and CYP3A7 rs10211 showed an increased risk of CRC (OR 1.26 and 1.38, respectively; two-sided p≤0.05), whereas carriers of the ancestral allele of ENPP1 rs1044498 had a decreased risk (OR 0.79; p≤0.05). For rs1044498, the strongest association was detected in the Czech male subpopulation (OR 0.61; p=0.0015). The associations were not replicated in the German population. Signatures of selection were found for all three analyzed genes. CONCLUSIONS: Our study showed evidence of association for the ancestral alleles of polymorphisms in AGT and CYP3A7 and for the derived allele of a polymorphism in ENPP1 with an increased risk of CRC in Czechs, but not in Germans. The ancestral alleles of these SNPs have previously been associated with nutrition-related diseases hypertension (AGT and CYP3A7) and insulin resistance (ENPP1). Future studies may shed light on the complex genetic and environmental interactions between different types of nutrition-related diseases.
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spelling pubmed-35229992012-12-16 Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases Huhn, Stefanie Bevier, Melanie Rudolph, Anja Pardini, Barbara Naccarati, Alessio Hoffmeister, Michael Vodickova, Ludmila Novotny, Jan Brenner, Hermann Chang-Claude, Jenny Hemminki, Kari Vodicka, Pavel Försti, Asta BMC Med Genet Research Article BACKGROUND: The majority of non-syndromic colorectal cancers (CRCs) can be described as a complex disease. A two-stage case–control study on CRC susceptibility was conducted to assess the influence of the ancestral alleles in the polymorphisms previously associated with nutrition-related complex diseases. METHODS: In stage I, 28 single nucleotide polymorphisms (SNPs) were genotyped in a hospital-based Czech population (1025 CRC cases, 787 controls) using an allele-specific PCR-based genotyping system (KASPar®). In stage II, replication was carried out for the five SNPs with the lowest p values. The replication set consisted of 1798 CRC cases and 1810 controls from a population-based German study (DACHS). Odds ratios (ORs) and 95% confidence intervals (CIs) for associations between genotypes and CRC risk were estimated using logistic regression. To identify signatures of selection, Fay-Wu’s H and Integrated Haplotype Score (iHS) were estimated. RESULTS: In the Czech population, carriers of the ancestral alleles of AGT rs699 and CYP3A7 rs10211 showed an increased risk of CRC (OR 1.26 and 1.38, respectively; two-sided p≤0.05), whereas carriers of the ancestral allele of ENPP1 rs1044498 had a decreased risk (OR 0.79; p≤0.05). For rs1044498, the strongest association was detected in the Czech male subpopulation (OR 0.61; p=0.0015). The associations were not replicated in the German population. Signatures of selection were found for all three analyzed genes. CONCLUSIONS: Our study showed evidence of association for the ancestral alleles of polymorphisms in AGT and CYP3A7 and for the derived allele of a polymorphism in ENPP1 with an increased risk of CRC in Czechs, but not in Germans. The ancestral alleles of these SNPs have previously been associated with nutrition-related diseases hypertension (AGT and CYP3A7) and insulin resistance (ENPP1). Future studies may shed light on the complex genetic and environmental interactions between different types of nutrition-related diseases. BioMed Central 2012-10-05 /pmc/articles/PMC3522999/ /pubmed/23036011 http://dx.doi.org/10.1186/1471-2350-13-94 Text en Copyright ©2012 Huhn et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Huhn, Stefanie
Bevier, Melanie
Rudolph, Anja
Pardini, Barbara
Naccarati, Alessio
Hoffmeister, Michael
Vodickova, Ludmila
Novotny, Jan
Brenner, Hermann
Chang-Claude, Jenny
Hemminki, Kari
Vodicka, Pavel
Försti, Asta
Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
title Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
title_full Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
title_fullStr Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
title_full_unstemmed Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
title_short Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
title_sort shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522999/
https://www.ncbi.nlm.nih.gov/pubmed/23036011
http://dx.doi.org/10.1186/1471-2350-13-94
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