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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3522999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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