Document Detail

Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.
Jump to Full Text
MedLine Citation:
PMID:  23036011     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
Stefanie Huhn; Melanie Bevier; Anja Rudolph; Barbara Pardini; Alessio Naccarati; Rebecca Hein; Michael Hoffmeister; Ludmila Vodickova; Jan Novotny; Hermann Brenner; Jenny Chang-Claude; Kari Hemminki; Pavel Vodicka; Asta Försti
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2012-10-05
Journal Detail:
Title:  BMC medical genetics     Volume:  13     ISSN:  1471-2350     ISO Abbreviation:  BMC Med. Genet.     Publication Date:  2012  
Date Detail:
Created Date:  2012-12-17     Completed Date:  2013-02-27     Revised Date:  2013-07-11    
Medline Journal Info:
Nlm Unique ID:  100968552     Medline TA:  BMC Med Genet     Country:  England    
Other Details:
Languages:  eng     Pagination:  94     Citation Subset:  IM    
Affiliation:
Department of Molecular Genetic Epidemiology, German Cancer Research Center DKFZ, Heidelberg, Germany. s.huhn@dkfz.de
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Colorectal Neoplasms / genetics
Female
Gene-Environment Interaction
Genetic Predisposition to Disease
Humans
Male
Nutrition Disorders / genetics*
Polymorphism, Single Nucleotide
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Full Text
Journal Information
Journal ID (nlm-ta): BMC Med Genet
Journal ID (iso-abbrev): BMC Med. Genet
ISSN: 1471-2350
Publisher: BioMed Central
Article Information
Download PDF
Copyright ©2012 Huhn et al.; licensee BioMed Central Ltd.
open-access:
Received Day: 28 Month: 2 Year: 2012
Accepted Day: 28 Month: 9 Year: 2012
collection publication date: Year: 2012
Electronic publication date: Day: 5 Month: 10 Year: 2012
Volume: 13First Page: 94 Last Page: 94
PubMed Id: 23036011
ID: 3522999
Publisher Id: 1471-2350-13-94
DOI: 10.1186/1471-2350-13-94

Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
Stefanie Huhn1 Email: s.huhn@dkfz.de
Melanie Bevier1 Email: m.bevier@dkfz.de
Anja Rudolph2 Email: a.rudolph@dkfz.de
Barbara Pardini3 Email: superbab16@yahoo.it
Alessio Naccarati3 Email: alenacca@hotmail.com
Rebecca Hein28 Email: rebecca.hein@uk-koeln.de
Michael Hoffmeister4 Email: m.hoffmeister@dkfz.de
Ludmila Vodickova35 Email: ludovod@seznam.cz
Jan Novotny6 Email: onkologie@seznam.cz
Hermann Brenner4 Email: h.brenner@dkfz.de
Jenny Chang-Claude2 Email: j.chang-claude@dkfz.de
Kari Hemminki17 Email: K.Hemminki@dkfz.de
Pavel Vodicka35 Email: pvodicka@biomed.cas.cz
Asta Försti17 Email: A.Foersti@dkfz.de
1Department of Molecular Genetic Epidemiology, German Cancer Research Center DKFZ, Heidelberg 69120, Germany
2Division of Cancer Epidemiology, German Cancer Research Center DKFZ, Heidelberg 69120, Germany
3Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Prague, 14200, Czech Republic
4Division of Clinical Epidemiology and Aging Research, German Cancer Research Center DKFZ, Heidelberg, 69120, Germany
5Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University, Prague 2, 12000, Czech Republic
6Department of Oncology, General Teaching Hospital, Prague 2, 12808, Czech Republic
7Center of Primary Health Care Research, Clinical Research Center, Lund University, Malmö, SE-20502, Sweden
8PMV Forschungsgruppe, University of Cologne, Cologne, 50931, Germany

Background

Colorectal cancer (CRC; OMIM ID: 114500) is among the most common cancers in industrialized countries and one of the leading causes of cancer-related mortality [1]. The incidence rates vary among different groups and populations depending on sex, age and country, with higher rates among males than females and increasing with age [2]. The differences in the incidence rates across the globe are mainly attributed to differences in diet and other environmental factors.

In both sporadic and familial CRC, genes and environment together contribute to the risk of CRC. The majority of non-syndromic CRCs can be characterized as a complex disease [3]. The major factors that modify CRC risk are obesity, diabetes, red meat consumption, physical inactivity, alcohol consumption, chronic inflammation, and cigarette smoking [4-6]. Additionally, the intake of vitamin D, calcium, fruit and vegetables may potentially influence the risk of CRC [5]. Gene-environment interactions also underlie other complex diseases, such as obesity (OMIM ID: 601665) and diabetes mellitus type II (T2D; OMIM ID: 125853).

A specific feature of CRC and other complex diseases is that they are mainly diseases of humans living in industrialized societies, in environments with almost unlimited food supply and low energy expenditure [5,7]. Nutrition is one of the most important environmental traits influencing the fitness of an individual. In the past centuries, the genetic constitution of an individual was supposed to optimize food utilization in order to protect against malnutrition. In modern societies, the ancestral genetic constitution might not be beneficial anymore, because it does not protect against the relatively new condition of overnutrition. Therefore, variants that protect against overnutrition and related health issues are supposed to be rare [7]. Nevertheless, genetic variants that promote a carbohydrate-based nutrition as well as genetic variants that show ancestral susceptibility to a nutrition-related disease have already been described (inter alia [8-10]). Signatures of such processes can be detected in the human genome using genome-wide approaches that evaluate differences in the world-wide allele frequencies and haplotype distribution (inter alia [11-15]).

Based on the interplay between genetic and environmental risk factors in nutrition-related complex diseases we posed the following hypothesis: “Polymorphisms with ancestral alleles associating with a nutrition-related disease and showing signatures of recent selection may be associated with CRC risk.” We outline here the methods used for selecting such candidate genes and show the results when the selected variants were tested for CRC risk in two large case–control studies.


Methods
Candidate SNP selection for the case–control study

The study focused on SNPs, for which ancestral alleles have previously been associated with nutrition-related complex diseases other than CRC, such as obesity, T2D and metabolic syndrome. Information about such SNPs was collected from 30 published reports by browsing the PubMed database (http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed) [16] for the keywords “diabetes”, “obesity”, “metabolic syndrome” (OMIM ID: 605552) and “hypertension” (OMIM ID: 145500) up to 06/2009. Most of the articles were based on genome-wide association studies or were meta-analyses. A complete list of the publications can be found at the reference list of the Additional file1.

From these 30 reports, associations with the risk of the diseases and with the related quantitative traits were retrieved. The quantitative traits for diabetes were fasting glucose level and insulin resistance. For obesity, the traits were body mass index (BMI) and waist to hip ratio. The quantitative traits for hypertension and the metabolic syndrome were high-density lipoprotein (HDL) level, low-density lipoprotein (LDL) level, triglycerides level, salt sensitivity, blood pressure and insulin resistance. A complete list of the reported associations can be found in the Additional file 1.

The candidate SNP selection for the association study took place in three major phases (Figure 1):

(1) “Selection of Candidate SNPs”: All published SNPs were evaluated for the nature of the risk allele – either ancestral (A) or derived (D) - and the allele frequency differences between African, European and Asian populations (YRI: Sub-Saharan African population, Yoruba in Ibadan, Nigeria; CEU: Caucasian population, Utah residents with Northern and Western European ancestry from the CEPH collection; HCB: East Asian population, Han Chinese in Beijing, China; JPT: East Asian population, Japanese in Tokyo, Japan). An allele was considered a “risk allele” when it was associated with a significantly increased risk of a key-disease (OR>1; statistical significance based on the criteria of the original publication), or when it was associated with a significant increase of quantitative values in the original publication. The nature of the risk allele was determined by using the NCBI database (http://www.ncbi.nlm.nih.gov) [16].

The reported ancestral susceptibility SNPs that showed an absolute allele frequency difference of >45% between the African and any non-African population were chosen for further investigation. The threshold value of 45% was set to detect variants with a “major-to-minor” allele change between populations, thus indicating a possible influence of selective pressure. A second, lower threshold (25%) was set for the difference between the YRI and the CEU population to acknowledge the more recent separation of the European than the East Asian population from the African population.

(2) “Candidate Gene Definition”: The SNPs that passed the first selection criteria were evaluated for their location in the genome, possible functional effects, linkage disequilibrium (LD) with other polymorphisms within the gene region and the number of candidate SNPs in the gene region.

(3) “Tagging SNP Approach”: In addition to the evaluation of the reported ancestral susceptibility SNPs, a tagging SNP approach was carried out for each candidate gene or gene region using the genotyping data of the CEU population and HaploView© software [17]. Next to a minor allele frequency (MAF) of ≥5%, a tagging SNP had to feature the following parameters:

– be or capture a phase 1 SNP and/or

– be or capture a functional polymorphism and/or

– capture a maximal number of SNPs within a candidate gene or gene region with >25% allele frequency difference between the YRI and the CEU population

In the majority of cases, the reported ancestral susceptibility SNP itself was genotyped. When that was not possible (e.g. because the assay design failed due to the structure of the surrounding sequence) another SNP that was in LD with the reported SNP (r2>0.9) was selected for genotyping in order to indirectly gain information about the reported ancestral susceptibility SNP. For large, diverse genes/gene clusters, additional tagging SNPs were selected in order to gain more knowledge about the genes. These tagging SNPs should also fulfil the criterion of >25% allele frequency difference between the YRI and CEU population (Table 1).

Allele frequencies were obtained from the NCBI database for the submitter population IDs: HapMap -CEU, -YRI, -HCB and -JPT (NCBI dbSNP Build 130; http://www.ncbi.nlm.nih.gov) [16]. LD/r2 was obtained from HapMap using the HapMap3 - and HapMart Genome Browser (Release #2, Phase 3; http://hapmap.ncbi.nlm.nih.gov) [28,29] and HaploView© software (Version 3, Release 2, Analyse Panel CEU) [17] with the implemented Tagger tagSNP selection algorithm [30]. The data about possible functionality originate from the NCBI database (http://www.ncbi.nlm.nih.gov) [16] and the PolyPhen (http://genetics.bwh.harvard.edu/pph/) [inter alia [31].

Study populations

First, a hospital-based study population from the Czech Republic was analyzed. Between 09/2004 and 05/2009, 1025 CRC cases were recruited by nine oncological departments in the Czech Republic [32]. The sampled patients showed positive colonoscopic results for malignancy, histologically confirmed as colon or rectal carcinomas. The patients who met the Amsterdam criteria I or II for hereditary nonpolyposis colorectal cancer (OMIM ID: 120435) were excluded from the study. During the same time period, 787 healthy controls were recruited by five gastroenterological departments of the Czech Republic [32]. They were individuals undergoing colonoscopy for various gastrointestinal complaints, such as macroscopic bleeding, positive faecal occult blood test or abdominal pain of unknown origin. Only individuals showing negative colonoscopic results for malignancies, colorectal adenomas, benign polyps or inflammatory bowel disease were eligible for the study. Beside general information about sex and age, information about BMI (OMIM ID: 606641) and diabetes status was available for most of the individuals (Table 2).

The SNPs that showed nominally significant associations in the Czech population were additionally analysed in a German population-based case–control study. The DACHS (Darmkrebs: Chancen der Verhütung durch Screening) study contributed 1798 cases and 1810 matched controls recruited from 01/2003 to 12/2007 in South-West Germany [33,34]. The patients included in the study had a first diagnosis of invasive CRC. As controls, individuals were randomly selected from lists of residents provided by the population registries. In the detailed standardized questionnaires, information about BMI at least five years before sampling and diabetes status was available in addition to general information about sex and age [34]. Table 2 outlines the characteristics of the Czech and the DACHS population relevant for the study.

Ethical standards

The study was approved by the Ethics Committees of the Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Prague (Czech Republic); Institute for Clinical and Experimental Medicine and Faculty, Thomayer Hospital, Prague (Czech Republic); Medical Faculty of the University of Heidelberg (Germany) and the State Medical Boards of Baden-Württemberg and Rheinland-Pfalz (Germany). Written informed consent was obtained from all study participants.

Genotyping

Genotyping was performed using a competitive allele-specific PCR genotyping system (KASPar®; KBiosciences, UK). PCR reactions were carried out in a 384-plate format using 3ng DNA per reaction in a 4μl reaction volume according to the optimal PCR protocol suggested by KBiosciences. The genotype detection was performed using an ABI PRISM 7900-HT Sequence Detection System with SDS 2.2 software (Applied Biosystems). For internal quality control, 7% of the Czech samples and 5% of the DACHS samples were randomly selected and included as duplicates. The concordance rate between the original and the duplicate samples was ≥ 99%. The average call rate was 98.2% in the Czech population and 97.1% in the DACHS population.

Statistical analysis

The observed genotype frequencies in the controls were tested for Hardy-Weinberg equilibrium (HWE) using χ2 tests [35]. Odds ratios (ORs) and 95% confidence intervals (CIs) for associations between genotypes and CRC risk were estimated by logistic regression (PROC LOGISTIC, SAS Version 9.2; SAS Institute, Cary, NC) [36]. The estimated effects for all SNPs refer to the ancestral allele (A). Due to the low allele frequency shown by the majority of the tested polymorphisms the dominant model was applied in all estimations. The ORs were adjusted for age and sex. Additionally, a pooled analysis of the two studies was conducted. The ORs for the pooled analysis were adjusted for age, sex and study population.

Gene-gene interaction was studied for pair-wise interaction using logistic regression. To acknowledge the fact that men are in higher risk for CRC than women and that BMI is one of the most important risk factors for non-syndromic CRC, an analysis stratified by sex and BMI was performed. The threshold value for BMI was chosen according to the median BMI in the respective study population. To assess effect modification by sex and BMI, multiplicative interaction terms were utilized in multivariate regression models.

P values ≤ 0.05 were considered statistically significant. Bonferroni correction was not applied because it would have been overly conservative since the SNP selection was hypothesis-driven and all selected SNPs have previously been associated with a phenotype predisposing to CRC. Instead, a replication study using the German sample population was conducted to validate the initial results in the Czech population.

Signatures of selection

Next to allele frequency differences between the African and the non-African populations, the study aimed to detect additional signatures of selection in those genes that were associated with CRC in the case–control study. Highly variable allele frequencies in different populations might be attributable to processes such as genetic drift, bottleneck events or founder effects that occur during the separation from the ancestral population. In order to encounter this problem, methods, which are less susceptible to demographic influences, were applied to investigate signatures of selective pressure. Instead of the traditional FST value and Tajiman D test, Fay-Wu’s H and the Standardized Integrated Haplotype Score (|iHS|) were estimated using the Haplotter web application that was developed on genome-wide HapMap data (http://haplotter.uchicago.edu/) [13,15]. The Fay-Wu’s H algorithm detects unusual excess of high frequency derived alleles in a gene region. Strong negative Fay-Wu’s H values are considered as signatures for a selective sweep [12,15]. The iHS measures the length of haplotypes around a given SNP in comparison to the whole genome. Values < −1.5 and > 1.5 (|1.5|) give conclusive evidence for natural selection while values < −2 or > 2 (|2.0|) give evidence for a powerful selection signal [15,37]. Values were estimated for the YRI, the CEU and the East Asian (ANS) population.


Results
Candidate SNP selection

With the keywords “diabetes”, “obesity”, “metabolic syndrome” and “hypertension”, we found in PubMed 30 publications, which reported 246 polymorphisms to be associated with the key-disease or with a related quantitative trait. Supplementary material (Additional file 1) provides information about all the 246 polymorphisms with the corresponding chromosomal position, allele status and frequency, reported associations with the diseases or the traits, information about the functionality of the SNPs and a complete reference list.

Carriers of the ancestral (A) allele of 130 SNPs had an increased risk of a key-disease (52.8%), whereas 106 SNPs were associated with an increased risk due to the derived (D) allele. The majority of the SNPs were located in introns (all 43.1%; A 48.5%; D 40.6%) or intergenic regions (all 38.6%; A 34.6%; D 47.2%). Less than 15% of all SNPs (A 17%; D 13%) were nonsense, missense, cds-synonymous or UTR SNPs.

The frequency differences estimated for the ancestral susceptibility alleles among the four worldwide populations were highly variable (YRI vs. any: mean 34.8; range 0.0-94.4; YRI vs. CEU: mean 20.7; range 0.0-87.3). Twenty-nine SNPs fulfilled the selection criteria of allele frequency difference >45% between the African and the non-African populations and >25% between the YRI and the CEU populations. These SNPs with their corresponding genes were considered as candidates for the CRC case–control study. After considering the location and the function of the SNPs and the LD characteristics of the gene regions, 28 SNPs in 15 genes were selected for the case–control study (Table 1).

Association study

The genotype distribution of 27 of the 28 SNPs genotyped in the Czech control population was according to HWE. For ERBB3 rs11171739, the genotype distribution deviated from HWE (p <0.0001) and the SNP was not considered in the further analyses. Except for CYP3A5 rs776746, which was monomorphic in the Czech cohort, none of the observed allele frequencies differed significantly from the allele frequencies given in the NCBI database (CEU population).

Three SNPs in three genes showed modest associations with the risk of CRC in the Czech population (Table 3). The ancestral alleles of two SNPs were associated with an increased risk of CRC: AGT rs699 (OR 1.26; 95% CI 1.01-1.57) and CYP3A7 rs10211 (OR 1.38; 95% CI 1.04-1.83). In contrast, the ancestral allele of ENPP1 rs1044498 SNP was associated with a decreased risk of CRC (OR 0.79; 95% CI 0.63-1.00). The gene-gene interaction analysis showed no evidence of epistasis (data not shown).

A replication study in the German DACHS population was carried out for the five SNPs with the lowest p values (rs699, rs10211, rs1044498, rs12592797, rs7298565). None of the analysed polymorphisms were associated with the risk of CRC in the German population alone or in the pooled analysis of the two populations (Figure 2).

In the data stratified by sex, ENPP1 rs1044498 was associated with a decreased risk of CRC in the male subgroup of the Czech population (OR 0.61; 95% CI 0.45 - 0.83; p 0.0015; pinteraction 0.01). No association was detected in the Czech female subgroup and in the German study (data not shown).

In the data stratified by BMI, modest associations were detected in the Czech subgroup with a BMI >27 for AGT rs699 (OR 1.54; CI 1.05 - 2.25; p 0.027; pinteraction 0.036) and CYP3A7 rs10211 (OR 1.78; CI 1.08 - 2.93; p 0.023; pinteraction 0.113). No association was detected in the German study (data not shown).

Signatures of selection

One important signature of selective pressure was already a criterion to select the SNPs for the study: a high allele frequency difference between HapMap populations. Thus, all SNPs that were associated with the risk of CRC fulfilled this criterion. The highest allele frequency difference among all analysed SNPs was found in ENPP1 rs1044498 (YRI vs. HCB 94.4%; YRI vs. CEU 87.3%). The SNPs AGT rs699 and CYP3A7 rs10211 showed an allele frequency difference of 52.5% and 67% (YRI vs. CEU), respectively.

Fay-Wu’s H and |iHS| were analysed as further signatures of selection. All estimates of Fay-Wu’s H and |iHS| refer to SNPs that are linked to the genotyped SNPs (r2=1.0), because direct values were not available in the Haplotter web application http://haplotter.uchicago.edu/[13,15]. Signatures of a selective sweep indicated by Fay-Wu’s H were found for CYP3A7 rs2687075 (r2 to rs10211=1.0), with strong negative H estimates in the ANS population (−28.8) and in the CEU population (−49.6). The other two analysed polymorphisms did not show strong negative H values (> −8.0) or even showed positive values (Figure 3a). Values of |iHS| >1.5 that give conclusive evidence for natural selection in the CEU population were found for SNPs in AGT (rs2148582, r2 = 1.0 to rs699; |iHS| = 1.62), ENPP1 (rs6926970, r2 = 1.0 to rs1044498; |iHS| = 1.58) and CYP3A7 (rs2687075, r2 = 1.0 to rs10211; |iHS| = 1.67) (Figure 3b).


Discussion

The present study intended to crosslink susceptibility variants of nutrition-related complex diseases to CRC. In fact, the results in the Czech hospital-based case–control study suggested that polymorphisms in AGT, CYP3A7 and ENPP1 may be associated with the risk of CRC. However, replication in the population-based German DACHS population did not confirm the associations.

From the 246 SNPs that have been reported to be associated with a nutrition-related disease, 130 showed ancestral susceptibility to overall risk of obesity, T2D, metabolic syndrome or hypertension. However, only 29 SNPs fulfilled the initial selection criterion of ≥45% allele frequency difference between the YRI and any HapMap population, indicating selective pressure. Except ABCA1 that has been found to be mutated in CRC tumour samples [38,39], none of the 15 genes of the present study has previously been associated with the risk of CRC (http://www.ncbi.nlm.nih.gov/; http://www.hugenavigator.net/ CancerGEMKB/home.do) [40].

The association study in the Czech population indicated ancestral susceptibility to the risk of CRC for the missense AGT SNP rs699 and to the 3’UTR SNP rs10211 in CYP3A7. Interestingly, SNPs in these two genes feature similar phenotypic effects, such as predisposing to hypertension and salt sensitivity [18].

Published data about AGT suggests that the ancestral allele of the probable pathogenic SNP rs699 (M268T), as well as the ancestral alleles of the missense SNP rs4762 (T207M) and the 5′UTR SNP rs5051, predispose to essential hypertension, increased plasma angiotensinogen and increased frequency of preeclampsia (OMIM ID: 189800) [18,41,42]. Additionally, rs5051 (r2=0.95 to rs699) has been demonstrated to affect the transcription rate of AGT[41,42]. AGT (angiotensinogen [serpin peptidase inhibitor, clade A, member 8]) is an important member of the renin-angiotensin system that regulates blood pressure and fluid homeostasis probably through influencing sodium sensitivity [41,42].

Also the intronic CYP3A5 SNP rs776746 has previously been associated with hypertension and salt sensitivity [9,18]. This SNP has been reported to result in an incorrectly spliced mRNA and in a truncated non-functional protein. In the Czech population, rs776746 was monomorphic. However, the CYP3A7 SNP rs10211 - also located within the same cytochrome P450 gene cluster and linked to rs776746 in the HapMap CEU population (r2=0.82) - showed nominally significant association with the risk of CRC. The genes of the cytochrome P450 gene family encode for some of the most important enzymes involved in the metabolism of various xenobiotics and endogenous substrates such as cholesterol, steroids, environmental carcinogens and drugs [43]. In particular, CYP3 enzymes are responsible for the metabolism of eicosanoids.

The allele frequencies of the genotyped SNPs rs699 and rs10211 and the two functional SNPs rs5051 and rs776746 are highly variable among worldwide populations, with higher frequencies of the derived alleles in non-African populations while the ancestral alleles predominate in the African population. The values of |iHS| determined for SNPs that are fully linked to rs699 and rs10211 provided conclusive evidence for natural selection in the population with European ancestry. Additionally, rs2687075 (r2=1.0 to rs10211) in CYP3A7 showed strong negative values of Fay-Wu’s H that were considered as signatures for a selective sweep in non-African populations [12,15]. Previous studies have already suggested AGT and CYP3A5 as targets of selection, and have additionally connected the two genes directly by their related function [18,42]. In AGT, selection was particularly suggested to work on the promoter that contains rs699 and on SNPs in high LD with it. This selection was attributed to altered requirements for the human to maintain sodium homeostasis [42]. Since the derived allele, that predisposes to salt tolerance, is not yet fixed in non-African populations, the remaining ancestral allele, that predisposes to salt sensitivity, shows ancestral susceptibility to related diseases such as hypertension, preeclampsia [41,42] and CRC.

A possible association with the risk of CRC and signatures of recent selection were also observed for one polymorphism in ENPP1. However, in contrast to the initial hypothesis, the ancestral allele of rs1044498 was associated with a decreased risk of CRC in the Czech population. ENPP1 is a member of the ecto-nucleotide pyrophosphatase/phosphodiesterase (ENPP) family. The encoded protein interacts with the insulin receptor thereby inhibiting subsequent signalling. In previous studies, the ancestral allele of the missense polymorphism rs1044498 (Q121K) has been associated with more vivid insulin receptor binding, stronger inhibition of insulin signalling, insulin resistance, an increased risk of T2D and an increased risk of myocardial infarction (OMIM ID: 608446) [9,44,45]. The associations were most pronounced in cohorts that underwent lifestyle interventions to improve an individual’s weight or cholesterol level [45]. It is possible that the effect of ENPP1 on the risk of metabolic syndrome and the risk of CRC is highly dependent on additional environmental factors or modifiers.

Unfortunately, we were not able to validate our results in the independent German case–control study. Since the Czech and the German populations should not differ significantly in their genetic constitution, differences in nutrition or other environmental factors may contribute to the observed results or the associations may be a chance finding [46,47]. Since the selection of candidate SNPs was based on complex gene-environmental interactions - with the SNP contributing to a phenotype that predisposes to CRC - the detected associations are expected to be weaker than the associations for the original intermediate phenotype. Already in the original reports about the associations of SNPs with nutrition-related diseases, low ORs were detected in most of the cases. As we studied only a few polymorphisms per gene, other polymorphisms with low LD (r2<0.8) or rare SNPs (MAF<0.05) that may contribute to the risk of CRC might have been missed. However, considering previously reported associations of several SNPs in the three described genes with components of the metabolic syndrome, the ancestral nature of the risk alleles, and the detected signatures of selection, a true nature of the modest effects on CRC risk in the Czech population cannot be excluded [48]. Especially the close resemblance of the detected associations and function of SNPs in AGT and CYP3A7 may indicate a true effect of the polymorphisms on CRC susceptibility.


Conclusion

Our study showed evidence of association of the ancestral alleles of polymorphisms in AGT and CYP3A7 and 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 the 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. The application of additional selection criteria, such as ancestral susceptibility, signatures of selection, or pathway membership, might help to narrow down the numerous published polymorphisms and to find the most promising candidates for association studies. Large study populations that provide the possibility to define large subgroups with specific pre-diagnostic features may be used to review the actual function of such polymorphisms and may provide further insights into the evolution of common complex diseases.


Competing interests

The authors declare that they have no competing interests.


Authors’ contributions

The concept and design of the experiments was conceived by SH, AF, and KH. The experiments which provided the basis to this study were performed by SH. Statistical analyses in the association studies and population genetics were performed by SH, MB, AR, RH and AF. The sample collection and database management for the Czech study population was organized and performed by BP, AN, LV, JN and PV. The sample collection and database management for the DACHS study population was organized by MH, HB and JC-C. The manuscript was written by SH and AF. All authors revised the manuscript and contributed to the discussion of the results. The final manuscript was read and approved by all authors.


Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2350/13/94/prepub


Supplementary Material Additional file 1

Shared Ancestral Susceptibility to Colorectal Cancer.pdf. Title and description of the dataset: Table I. Information about genes and SNPs considered as candidates for the case–control study.



Acknowledgement

This study was supported by the German National Genome Research Network (NGFN-Plus). In the Czech Republic, the study was supported by Grant agency of the Czech Republic (GACR) [CZ:GACR:GA P304/10/1286 and P304/12/1585]. The DACHS Study was supported by grants from the German Research Council (Deutsche Forschungsgemeinschaft, grant numbers BR 1704/6-1, BR 1704/6-3, BR 1704/6-4 and CH 117/1-1), and the German Federal Ministry of Education and Research (grant numbers 01KH0404 and 01ER0814).


References
Ferlay J,Shin HR,Bray F,Forman D,Mathers C,Parkin DM,Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008Int J CancerYear: 2010127122893291721351269
Jemal A,Siegel R,Ward E,Hao Y,Xu J,Murray T,Thun MJ,Cancer statistics, 2008CA Cancer J ClinYear: 2008582719618287387
Laland KN,Odling-Smee J,Myles S,How culture shaped the human genome: bringing genetics and the human sciences togetherNat Rev GenetYear: 201011213714820084086
Bernstein CN,Blanchard JF,Kliewer E,Wajda A,Cancer risk in patients with inflammatory bowel disease: a population-based studyCancerYear: 200191485486211241255
Huxley RR,Ansary-Moghaddam A,Clifton P,Czernichow S,Parr CL,Woodward M,The impact of dietary and lifestyle risk factors on risk of colorectal cancer: a quantitative overview of the epidemiological evidenceInt J CancerYear: 2009125117118019350627
Il'yasova D,Colbert LH,Harris TB,Newman AB,Bauer DC,Satterfield S,Kritchevsky SB,Circulating levels of inflammatory markers and cancer risk in the health aging and body composition cohortCancer Epidemiol Biomarkers PrevYear: 200514102413241816214925
Bellisari A,Evolutionary origins of obesityObes RevYear: 20089216518018257754
Chen R,Corona E,Sikora M,Dudley JT,Morgan AA,Moreno-Estrada A,Nilsen GB,Ruau D,Lincoln SE,Bustamante CD,et al. Type 2 diabetes risk alleles demonstrate extreme directional differentiation among human populations, compared to other diseasesPLoS GenetYear: 201284e100262122511877
Di Rienzo A,Hudson RR,An evolutionary framework for common diseases: the ancestral-susceptibility modelTrends GenetYear: 2005211159660116153740
Hancock AM,Witonsky DB,Ehler E,Alkorta-Aranburu G,Beall C,Gebremedhin A,Sukernik R,Utermann G,Pritchard J,Coop G,et al. Colloquium paper: human adaptations to diet, subsistence, and ecoregion are due to subtle shifts in allele frequencyProc Natl Acad Sci USAYear: 2010107Suppl 28924893020445095
Coop G,Pickrell JK,Novembre J,Kudaravalli S,Li J,Absher D,Myers RM,Cavalli-Sforza LL,Feldman MW,Pritchard JK,The role of geography in human adaptationPLoS GenetYear: 200956e100050019503611
Fay JC,Wu CI,Hitchhiking under positive Darwinian selectionGeneticsYear: 200015531405141310880498
Oleksyk TK,Smith MW,O'Brien SJ,Genome-wide scans for footprints of natural selectionPhilos Trans R Soc Lond B Biol SciYear: 2010365153718520520008396
Tajima F,Statistical method for testing the neutral mutation hypothesis by DNA polymorphismGeneticsYear: 198912335855952513255
Voight BF,Kudaravalli S,Wen X,Pritchard JK,A map of recent positive selection in the human genomePLoS BiolYear: 200643e7216494531
The National Center for Biotechnology Information http://www.ncbi.nlm.nih.gov/.
Barrett JC,Fry B,Maller J,Daly MJ,Haploview: analysis and visualization of LD and haplotype mapsBioinformaticsYear: 200521226326515297300
Thompson EE,Kuttab-Boulos H,Witonsky D,Yang L,Roe BA,Di Rienzo A,CYP3A variation and the evolution of salt-sensitivity variantsAm J Hum GenetYear: 20047561059106915492926
Kathiresan S,Willer CJ,Peloso GM,Demissie S,Musunuru K,Schadt EE,Kaplan L,Bennett D,Li Y,Tanaka T,et al. Common variants at 30 loci contribute to polygenic dyslipidemiaNat GenetYear: 2009411566519060906
Willer CJ,Sanna S,Jackson AU,Scuteri A,Bonnycastle LL,Clarke R,Heath SC,Timpson NJ,Najjar SS,Stringham HM,et al. Newly identified loci that influence lipid concentrations and risk of coronary artery diseaseNat GenetYear: 200840216116918193043
The.Wellcome.Trust CCCGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsNatureYear: 2007447714566167817554300
Groop L,From fused toes in mice to human obesityNat GenetYear: 200739670670717534362
Bacci S,Ludovico O,Prudente S,Zhang YY,Di Paola R,Mangiacotti D,Rauseo A,Nolan D,Duffy J,Fini G,et al. The K121Q polymorphism of the ENPP1/PC-1 gene is associated with insulin resistance/atherogenic phenotypes, including earlier onset of type 2 diabetes and myocardial infarctionDiabetesYear: 200554103021302516186408
Yanagiya T,Tanabe A,Iida A,Saito S,Sekine A,Takahashi A,Tsunoda T,Kamohara S,Nakata Y,Kotani K,et al. Association of single-nucleotide polymorphisms in MTMR9 gene with obesityHum Mol GenetYear: 200716243017302617855449
Lo JC,Zhao X,Scuteri A,Brockwell S,Sowers MR,The association of genetic polymorphisms in sex hormone biosynthesis and action with insulin sensitivity and diabetes mellitus in women at midlifeAm J MedYear: 20061199 Suppl 1S69S7816949391
Benzinou M,Walley A,Lobbens S,Charles MA,Jouret B,Fumeron F,Balkau B,Meyre D,Froguel P,Bardet-Biedl syndrome gene variants are associated with both childhood and adult common obesity in French CaucasiansDiabetesYear: 200655102876288217003356
Meyre D,Delplanque J,Chevre JC,Lecoeur C,Lobbens S,Gallina S,Durand E,Vatin V,Degraeve F,Proenca C,et al. Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populationsNat GenetYear: 200941215715919151714
Altshuler DM,Gibbs RA,Peltonen L,Dermitzakis E,Schaffner SF,Yu F,Bonnen PE,de Bakker PI,Deloukas P,The.International.HapMap3.Consortiumet al. Integrating common and rare genetic variation in diverse human populationsNatureYear: 20104677311525820811451
The.International.HapMap.ConsortiumThe International HapMap ProjectNatureYear: 2003426696878979614685227
de Bakker PI,Yelensky R,Pe'er I,Gabriel SB,Daly MJ,Altshuler D,Efficiency and power in genetic association studiesNat GenetYear: 200537111217122316244653
Ramensky V,Bork P,Sunyaev S,Human non-synonymous SNPs: server and surveyNucleic Acids ResYear: 200230173894390012202775
Pechlivanis S,Bermejo JL,Pardini B,Naccarati A,Vodickova L,Novotny J,Hemminki K,Vodicka P,Forsti A,Genetic variation in adipokine genes and risk of colorectal cancerEur J EndocrinolYear: 2009160693394019273568
Brenner H,Chang-Claude J,Seiler CM,Rickert A,Hoffmeister M,Protection from colorectal cancer after colonoscopy: a population-based, case-control studyAnn Intern MedYear: 20111541223021200035
Sainz J,Rudolph A,Hein R,Hoffmeister M,Buch S,von Schonfels W,Hampe J,Schafmayer C,Volzke H,Frank B,et al. Association of genetic polymorphisms in ESR2, HSD17B1, ABCB1, and SHBG genes with colorectal cancer riskEndocr Relat CancerYear: 201118226527621317201
Emigh TH,A Comparison of Tests for Hardy-Weinberg EquilibriumBiometricsYear: 1980364627642
Cornfield J,A Method of Estimating Comparative Rates from Clinical Data - Applications to Cancer of the Lung, Breast, and CervixJ Natl Cancer IYear: 195111612691275
Southam L,Soranzo N,Montgomery SB,Frayling TM,McCarthy MI,Barroso I,Zeggini E,Is the thrifty genotype hypothesis supported by evidence based on confirmed type 2 diabetes- and obesity-susceptibility variants?DiabetologiaYear: 20095291846185119526209
Sjoblom T,Jones S,Wood LD,Parsons DW,Lin J,Barber TD,Mandelker D,Leary RJ,Ptak J,Silliman N,et al. The consensus coding sequences of human breast and colorectal cancersScienceYear: 2006314579726827416959974
Wood LD,Parsons DW,Jones S,Lin J,Sjoblom T,Leary RJ,Shen D,Boca SM,Barber T,Ptak J,et al. The genomic landscapes of human breast and colorectal cancersScienceYear: 200731858531108111317932254
Yu W,Gwinn M,Clyne M,Yesupriya A,Khoury MJ,A navigator for human genome epidemiologyNat GenetYear: 200840212412518227866
Inoue I,Nakajima T,Williams CS,Quackenbush J,Puryear R,Powers M,Cheng T,Ludwig EH,Sharma AM,Hata A,et al. A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitroJ Clin InvestYear: 1997997178617979120024
Nakajima T,Wooding S,Sakagami T,Emi M,Tokunaga K,Tamiya G,Ishigami T,Umemura S,Munkhbat B,Jin F,et al. Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the worldAm J Hum GenetYear: 200474589891615077204
Nebert DW,Dalton TP,The role of cytochrome P450 enzymes in endogenous signalling pathways and environmental carcinogenesisNat Rev CancerYear: 200661294796017128211
McAteer JB,Prudente S,Bacci S,Lyon HN,Hirschhorn JN,Trischitta V,Florez JC,The ENPP1 K121Q polymorphism is associated with type 2 diabetes in European populations: evidence from an updated meta-analysis in 42,042 subjectsDiabetesYear: 20085741125113018071025
Müssig K,Heni M,Thamer C,Kantartzis K,Machicao F,Stefan N,Fritsche A,Haring HU,Staiger H,The ENPP1 K121Q polymorphism determines individual susceptibility to the insulin-sensitising effect of lifestyle interventionDiabetologiaYear: 201053350450920091022
Lao O,Lu TT,Nothnagel M,Junge O,Freitag-Wolf S,Caliebe A,Balascakova M,Bertranpetit J,Bindoff LA,Comas D,et al. Correlation between genetic and geographic structure in EuropeCurr BiolYear: 200818161241124818691889
Nelis M,Esko T,Magi R,Zimprich F,Zimprich A,Toncheva D,Karachanak S,Piskackova T,Balascak I,Peltonen L,et al. Genetic structure of Europeans: a view from the North-EastPLoS OneYear: 200945e547219424496
Calle EE,Kaaks R,Overweight, obesity and cancer: epidemiological evidence and proposed mechanismsNat Rev CancerYear: 20044857959115286738

Figures

[Figure ID: F1]
Figure 1 

Workflow for the selection of candidate SNPs for the ancestral susceptibility project.



[Figure ID: F2]
Figure 2 

Comparative data plot of the OR and 95% CI of the SNPs analyzed in the Czech and the DACHS cohort; dominant model, individual Czech and DACHS data adjusted for age and sex; joint data adjusted for age and sex, stratified by study; CZ Czech cohort; OR odds ratio; CI confidence interval.



[Figure ID: F3]
Figure 3 

Plot of Fay-Wu’s H (a) and plot of the Standardized Integrated Haplotype Score (|iHS|) (b). Estimates for the SNPs that were associated with CRC in the Czech population. Comparison of the African (YRI), European (CEU) and East Asian (ANS) population. All estimates refer to SNPs that are linked to the genotyped SNPs because direct values were not available for the genotyped SNPs. * indicate values that provide conclusive evidence for natural selection [12,15,37].



Tables
[TableWrap ID: T1] Table 1 

Information about genes and SNPs selected for the SNP association study


Closest Candidate Gene rs Numbera(r2)b Status (reported / genotyped) Position SNPsc(ancestral / derived) Reported associationd Max. allele frequency difference (YRI vs. any) Allele frequency difference YRI vs. CEU Function or location Ref.
AGT Angiotensin I
rs699
R/G
Chr1: 228.912.667
C/T
Hypertension, Preeclampsia
52,5%
52,5%
missense
[9,18]
 
rs4762
R
Chr1: 228.912.850
C/T
Hypertension
3,3%
3,3%
missense
 
 
rs5051 (r2 0.948 to rs699)
R
Chr1: 228.916.745
A/G
Hypertension
52,1%
52,1%
5′UTR
 
GALNT2 Polypeptide N-acetylgalactosaminyl-transferase 2
rs4846914
R/G
Chr1: 228.362.564
G/A
HDL
58,0%
58,0%
intron
[19,20]
rs611229
G
Chr1: 228.390.690
G/T
tagging SNP
39,4%
39,4%
intron
-
 
rs2144300 (r2 0.933 to rs4846914)
R
Chr1: 228.361.789
C/T
HDL, Triglycerides
57,0%
57,0%
intron
[20]
IFIH1 Interferon induced with helicase C domain 1
rs1990760
R/G
Chr2: 162.832.547
C/T
T2D
54,0%
54,0%
missense / benign
[21]
SLC2A Solute carrier family 2, facilitated glucose transporter member 2
rs5400
R/G.
Chr3: 172.215.244
T/C
T2D
48,1%
35,0%
missense / damaging
[9]
rs6785233
G
Chr3: 172.239.679
G/T
tagging SNP
50,8%
38,3%
-
-
 
rs8192675
G
Chr3: 172.207.577
G/A
tagging SNP
76,7%
50,0%
-
-
IGF2BP2 Insulin-like growth factor 2 mRNA binding
rs1470579
R/G
Chr3: 187.012.024
C/A
T2D
60,0%
56,8%
intron
[22]
ENPP1 Ectonucleotide pyrophosphatase
rs1044498
R/G
Chr6: 132.214.311
C/A
Insulin resistance, T2D (early onset), Myocardial infarction (early onset)
94,4%
87,3%
missense / benign
[9,23]
 
rs9493119
G
Chr6: 132.253.111
G/A
tagging SNP
30,0%
20,8%
-
-
CYP3A_ Locus Cytochrom P450
rs776746
R/G.
Chr7: 99.108.725
A/G
Hypertension; Salt sensitivity
79,2%
79,2%
CYP3A5_ intron
[9,18]
rs10211
G
Chr7: 99.140.930
G/A
tagging SNP
67,0%
67,0%
3′UTR_CYP3A7
-
 
rs667660
G
Chr7: 99.257.162
C/A
tagging SNP
74,3%
74,3%
upstream CYP3a3
-
MTMR9 Myotubularin related protein 9
rs10091637
G
Chr8: 11.181.724
C/T
tagging SNP
36,9%
29,2%
intron
-
rs11250127
G
Chr8: 11.207.619
G/A
tagging SNP
66,4%
26,5%
intron
-
 
rs2293855 (r2 1.00 to rs11250127)
R
Chr8: 11.215.070
G/A
Obesity
64,2%
25,2%
intron
[24]
ABCA1 ATP-binding cassette transporter
rs4149268
R/G.
Chr9: 106.687.291
T/C
HDL
51,0%
46,0%
intron
[20]
rs4149274
R
Chr9: 106.679.485
A/G
HDL
4,0%
2,0%
intron
[20]
 
rs1883025
R
Chr9: 106.704.372
T/C
HDL
13,5%
10,0%
intron
[19]
GAD2 Glutamate decarboxylase 2
rs2236418
R/G.
Chr10: 26.545.752
G/A
Obesity
74,9%
74,9%
5′UTR
[9]
rs2839670
G
Chr10: 26.544.346
A/C
tagging SNP
60,0%
60,0%
upstream
-
rs6482538
G
Chr10: 26.549.870
G/A
tagging SNP
63,6%
63,6%
intron
-
rs7076544
G
Chr10: 26.597.731
G/A
tagging SNP
68,0%
68,0%
intron
-
 
rs8190748
G
Chr10: 26.609.761
G/A
tagging SNP
60,20%
60,20%
intron
-
Chr 12q13 ERBB3 Avian erythroplastic leukemia viral oncogen homolog 3
rs11171739
R/G
Chr11: 54.757.142
C/T
T2D
56,0%
48,0%
ERBB3 ~4kb downstream
[21]
KCTD10 Potassium channel tetramerisation domain
rs7298565
G
Chr12: 108.421.917
A/G
tagging SNP
57,7%
24,1%
missense
-
 
rs2338104 (r2 0.98 to rs7298565)
R
Chr12: 108.379.801
G/C
HDL
45,0%
25,0%
KCTD10 intron; MYO1H ~9kb upstream
[19,20]
CYP19A1 / GLDN Cytochrom P450 / Gliomedin
rs2446405
R/G
Chr15: 49.434.335
A/T
Insulin Resistance
43,0%
43,0%
GLDN intron
[25]
rs12592797
G
Chr15: 49.426.928
A/C
tagging SNP
52,5%
52,5%
GLDN intron
-
 
rs2445761
G
Chr15: 49.402.908
C/T
tagging SNP
40,9%
40,9%
CYP19A1 intron
-
BBS4 Bardet-Biedl syndrome-4
rs7178130
R/G
Chr15: 70.765.505
G/A
Bardet-Biedl Syndrome; Obesity
50,0%
50,0%
upstream 5
[26]
C18orf8 / NCP1 Chromosome 18 open reading frame 8 / Niemann-Pick disease, type C1
rs891386
R/G
Chr18: 19.357.969
A/C
tagging SNP
42,5%
42,5%
CRC associated Protein
[27]
  rs1805081 (r2 0.84 to rs891386) R Chr18: 19.394.680 A/G BMI 46,7% 46,7% missense  

R reported SNP; G genotyped SNP; “R/G” reported and genotyped SNP. Max. maximal; BMI body mass index, T2D type 2 diabetes, LDL low-density lipoprotein, HDL high-density lipoprotein, Ref. reference a genotyped SNPs are indicated in bold; b pair-wise linkage disequilibrium between the SNPs, if reported SNP was not genotyped directly; c reported risk allele is indicated in bold-underlined; d Next to the keywords that were used to collect and select the candidate SNPs from the literature, the table also includes all reported associations with related quantitative traits.


[TableWrap ID: T2] Table 2 

Characteristics of the Czech and the DACHS study population, at the time of diagnosis for cases and at the time of sampling for controls


Characteristics Czech Cases Czech Controls p value DACHS Cases DACHS Controls p value
total
1025
787
 
1798
1810
 
male [n (%)]
594 [58%]
453 [58%]
0.35c
1052 [59%]
1078 [60%]
0.52c
female [n (%)]
399 [39%]
333 [42%]
 
746 [41%]
732 [40%]
 
missing sex information [n (%)]
32 [3%]
1 [0.1%]
 
0
 
 
median age [range]
63 [26–86]
55 [24–91]
<0.0001b
69 [33–94]
70 [34–98]
0.21b
missing age information [n (%)]
32 [3%]
1 [0.1%]
 
0
 
 
median BMIa [range]
27 [13–53]
26 [17-44]
0.49b
27 [17–50]
26 [16–46]
<0.0001b
missing BMIa information [n (%)]
312 [30%]
294 [37%]
 
28 [2%]
10 [0.6%]
 
diabetes [n (%)]
142 [14%]
62 [8%]
0.002c
326 [18%]
247 [14%]
0.0002c
diabetes no [n (%)]
598 [58%]
434 [55%]
 
1456 [82%]
1558 [86%]
 
missing diabetes information [n (%)] 285 [28%] 291 [37%]   16 [0.9%] 5 [0.3%]  

BMI, body mass index; a for case samples BMI five years before diagnosis; b Wilcoxon two sample test; c chi-square test.


[TableWrap ID: T3] Table 3 

Genotype distribution of the polymorphisms in the Czech population


Czech sample population
Gene
SNP
Allele
Genotype distribution (D-DA-A)
HWE
Dominant modela
Name ID. (D/A) Controls (N) Cases (N) Controls OR (95% CI) p value
AGT
rs699
T/C
225-354-181
244-492-226
0.07
1.26 (1.01-1.57)
0.04
GALNT2
rs4846914
A/G
291-348-114
372-450-142
0.55
1.03 (0.84-1.27)
0.76
GALNT2
rs611229
T/G
314-358-101
426-427-130
0.95
0.89 (0.73-1.09)
0.25
IFIH1
rs1990760
T/C
282-355-109
360-455-151
0.87
1.04 (0.85-1.28)
0.72
SLC2A2
rs5400
C/T
586-161-14
743-217-18
0.45
1.09 (0.86-1.38)
0.49
SLC2A2
rs6785233
T/G
643-120-6
828-146-8
0.88
0.99 (0.76-1.30)
0.95
SLC2A2
rs8192675
T/C
392-313-66
491-409-73
0.75
1.03 (0.85-1.26)
0.75
IGFBP2
rs1470579
A/C
389-290-82
494-376-104
0.01
1.01 (0.83-1.23)
0.91
ENPP1
rs1044498
A/C
573-184-19
773-200-13
0.36
0.79 (0.63-1.00)
0.05
ENPP1
rs9493119
A/G
720-54-1
916-69-5
0.99
1.17 (0.80-1.71)
0.42
CYP3A[x]
rs10211
A/G
668-97-4
820-150-8
0.81
1.38 (1.04-1.83)
0.03
CYP3A[x]
rs667660
A/C
668-93-4
830-144-8
0.70
1.24 (0.93-1.65)
0.14
MTMR9
rs10091637
T/C
174-394-194
229-496-257
0.34
0.97 (0.77-1.23)
0.79
MTMR9
rs11250127
A/G
105-376-290
150-431-388
0.33
0.87 (0.65-1.15)
0.32
ABCA1
rs4149268
G/A
309-363-94
398-458-119
0.42
1.02 (0.83-1.25)
0.87
GAD2
rs2236418
A/G
529-219-22
667-276-31
0.91
0.93 (0.75-1.15)
0.51
GAD2
rs2839670
C/A
526-217-22
672-277-35
0.95
0.94 (0.76-1.16)
0.57
GAD2
rs6482538
A/G
648-120-6
812-164-8
0.86
1.03 (0.80-1.35)
0.80
GAD2
rs7076544
A/G
520-230-20
645-304-34
0.36
1.02 (0.82-1.25)
0.88
GAD2
rs8190748
A/G
400-310-55
501-395-85
0.63
0.98 (0.80-1.19)
0.81
ERBB3
rs11171739
T/C
341-301-121
447-354-162
0.0001
 
 
KCTD10
rs7298565
G/A
158-349-248
185-449-344
0.09
1.19 (0.93-1.53)
0.16
CYP19A1
rs12592797
C/A
623-121-7
798-170-9
0.68
1.24 (0.95-1.61)
0.12
CYP19A1
rs2445761
A/G
275-352-130
353-456-148
0.34
1.00 (0.82-1.23)
0.98
CYP19A1
rs2446405
T/A
527-218-21
672-279-29
0.79
1.11 (0.90-1.38)
0.33
BBS4
rs7178130
A/G
280-366-110
388-454-129
0.59
0.88 (0.72-1.08)
0.21
NCP1 rs891286 C/A 145-364-203 194-471-304 0.43 1.09 (0.84-1.40) 0.52

A ancestral allele, D derived allele; N number; HWE Hardy Weinberg equilibrium, OR odds ratio; CI confidence interval; a adjusted for age and sex; bold numbers indicate statistical significance at 5% level.



Article Categories:
  • Research Article

Keywords: Colorectal cancer, Nutrition, Complex diseases.

Previous Document:  Visualizing the third dimension in virtual training environments for neurologically impaired persons...
Next Document:  Annotated genetic linkage maps of Pinus pinaster Ait. from a Central Spain population using microsat...