Genetic Variants Associated with Colorectal Adenoma Susceptibility

Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multiplicity (≥ 3 adenom...

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Published inPloS one Vol. 11; no. 4; p. e0153084
Main Authors Abulí, Anna, Castells, Antoni, Bujanda, Luis, Lozano, Juan José, Bessa, Xavier, Hernández, Cristina, Álvarez-Urturi, Cristina, Pellisé, Maria, Esteban-Jurado, Clara, Hijona, Elizabeth, Burón, Andrea, Macià, Francesc, Grau, Jaume, Guayta, Rafael, Castellví-Bel, Sergi, Andreu, Montserrat
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 14.04.2016
Public Library of Science (PLoS)
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Abstract Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multiplicity (≥ 3 adenomas). We selected 1,326 patients with increased risk for advanced adenomas and/or multiplicity and 1,252 controls with normal colonoscopy from population-based colorectal cancer screening programs. We conducted a case-control association study analyzing 30 colorectal cancer susceptibility variants in order to investigate the contribution of these variants to the development of subsequent advanced neoplasia and/or multiplicity. We found that 14 of the analyzed genetic variants showed a statistically significant association with advanced adenomas and/or multiplicity: the probability of developing these lesions increased with the number of risk alleles reaching a 2.3-fold risk increment in individuals with ≥ 17 risk alleles. Nearly half of the genetic variants associated with colorectal cancer risk are also related to advanced adenoma and/or multiplicity predisposition. Assessing the number of risk alleles in individuals within colorectal cancer screening programs may help to identify better a subgroup with increased risk for advanced neoplasia and/or multiplicity in the general population.
AbstractList BACKGROUNDCommon low-penetrance genetic variants have been consistently associated with colorectal cancer risk.AIMTo determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multiplicity (≥ 3 adenomas).METHODSWe selected 1,326 patients with increased risk for advanced adenomas and/or multiplicity and 1,252 controls with normal colonoscopy from population-based colorectal cancer screening programs. We conducted a case-control association study analyzing 30 colorectal cancer susceptibility variants in order to investigate the contribution of these variants to the development of subsequent advanced neoplasia and/or multiplicity.RESULTSWe found that 14 of the analyzed genetic variants showed a statistically significant association with advanced adenomas and/or multiplicity: the probability of developing these lesions increased with the number of risk alleles reaching a 2.3-fold risk increment in individuals with ≥ 17 risk alleles.CONCLUSIONSNearly half of the genetic variants associated with colorectal cancer risk are also related to advanced adenoma and/or multiplicity predisposition. Assessing the number of risk alleles in individuals within colorectal cancer screening programs may help to identify better a subgroup with increased risk for advanced neoplasia and/or multiplicity in the general population.
Background Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. Aim To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multiplicity ([greater than or equal to] 3 adenomas). Methods We selected 1,326 patients with increased risk for advanced adenomas and/or multiplicity and 1,252 controls with normal colonoscopy from population-based colorectal cancer screening programs. We conducted a case-control association study analyzing 30 colorectal cancer susceptibility variants in order to investigate the contribution of these variants to the development of subsequent advanced neoplasia and/or multiplicity. Results We found that 14 of the analyzed genetic variants showed a statistically significant association with advanced adenomas and/or multiplicity: the probability of developing these lesions increased with the number of risk alleles reaching a 2.3-fold risk increment in individuals with [greater than or equal to] 17 risk alleles. Conclusions Nearly half of the genetic variants associated with colorectal cancer risk are also related to advanced adenoma and/or multiplicity predisposition. Assessing the number of risk alleles in individuals within colorectal cancer screening programs may help to identify better a subgroup with increased risk for advanced neoplasia and/or multiplicity in the general population.
Background Common low-penetrance genetic variants have been consistently associated with colorec- tal cancer risk. Aim To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multi- plicity ( 3 adenomas). Methods We selected 1,326 patients with increased risk for advanced adenomas and/or multiplicity and 1,252 controls with normal colonoscopy from population-based colorectal cancer screening programs. We conducted a case-control association study analyzing 30 colorec- tal cancer susceptibility variants in order to investigate the contribution of these variants to the development of subsequent advanced neoplasia and/or multiplicity. Results We found that 14 of the analyzed genetic variants showed a statistically significant associa- tion with advanced adenomas and/or multiplicity: the probability of developing these lesions increased with the number of risk alleles reaching a 2.3-fold risk increment in individuals with 17 risk alleles. Conclusions Nearly half of the genetic variants associated with colorectal cancer risk are also related to advanced adenoma and/or multiplicity predisposition. Assessing the number of risk alleles in individuals within colorectal cancer screening programs may help to identify better a sub- group with increased risk for advanced neoplasia and/or multiplicity in the general population.
Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multiplicity ([greater than or equal to] 3 adenomas). We selected 1,326 patients with increased risk for advanced adenomas and/or multiplicity and 1,252 controls with normal colonoscopy from population-based colorectal cancer screening programs. We conducted a case-control association study analyzing 30 colorectal cancer susceptibility variants in order to investigate the contribution of these variants to the development of subsequent advanced neoplasia and/or multiplicity. We found that 14 of the analyzed genetic variants showed a statistically significant association with advanced adenomas and/or multiplicity: the probability of developing these lesions increased with the number of risk alleles reaching a 2.3-fold risk increment in individuals with [greater than or equal to] 17 risk alleles. Nearly half of the genetic variants associated with colorectal cancer risk are also related to advanced adenoma and/or multiplicity predisposition. Assessing the number of risk alleles in individuals within colorectal cancer screening programs may help to identify better a subgroup with increased risk for advanced neoplasia and/or multiplicity in the general population.
Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multiplicity (≥ 3 adenomas). We selected 1,326 patients with increased risk for advanced adenomas and/or multiplicity and 1,252 controls with normal colonoscopy from population-based colorectal cancer screening programs. We conducted a case-control association study analyzing 30 colorectal cancer susceptibility variants in order to investigate the contribution of these variants to the development of subsequent advanced neoplasia and/or multiplicity. We found that 14 of the analyzed genetic variants showed a statistically significant association with advanced adenomas and/or multiplicity: the probability of developing these lesions increased with the number of risk alleles reaching a 2.3-fold risk increment in individuals with ≥ 17 risk alleles. Nearly half of the genetic variants associated with colorectal cancer risk are also related to advanced adenoma and/or multiplicity predisposition. Assessing the number of risk alleles in individuals within colorectal cancer screening programs may help to identify better a subgroup with increased risk for advanced neoplasia and/or multiplicity in the general population.
Background Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. Aim To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multiplicity (≥ 3 adenomas). Methods We selected 1,326 patients with increased risk for advanced adenomas and/or multiplicity and 1,252 controls with normal colonoscopy from population-based colorectal cancer screening programs. We conducted a case-control association study analyzing 30 colorectal cancer susceptibility variants in order to investigate the contribution of these variants to the development of subsequent advanced neoplasia and/or multiplicity. Results We found that 14 of the analyzed genetic variants showed a statistically significant association with advanced adenomas and/or multiplicity: the probability of developing these lesions increased with the number of risk alleles reaching a 2.3-fold risk increment in individuals with ≥ 17 risk alleles. Conclusions Nearly half of the genetic variants associated with colorectal cancer risk are also related to advanced adenoma and/or multiplicity predisposition. Assessing the number of risk alleles in individuals within colorectal cancer screening programs may help to identify better a subgroup with increased risk for advanced neoplasia and/or multiplicity in the general population.
Background Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. Aim To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multiplicity (≥ 3 adenomas). Methods We selected 1,326 patients with increased risk for advanced adenomas and/or multiplicity and 1,252 controls with normal colonoscopy from population-based colorectal cancer screening programs. We conducted a case-control association study analyzing 30 colorectal cancer susceptibility variants in order to investigate the contribution of these variants to the development of subsequent advanced neoplasia and/or multiplicity. Results We found that 14 of the analyzed genetic variants showed a statistically significant association with advanced adenomas and/or multiplicity: the probability of developing these lesions increased with the number of risk alleles reaching a 2.3-fold risk increment in individuals with ≥ 17 risk alleles. Conclusions Nearly half of the genetic variants associated with colorectal cancer risk are also related to advanced adenoma and/or multiplicity predisposition. Assessing the number of risk alleles in individuals within colorectal cancer screening programs may help to identify better a subgroup with increased risk for advanced neoplasia and/or multiplicity in the general population.
Audience Academic
Author Álvarez-Urturi, Cristina
Castells, Antoni
Bessa, Xavier
Lozano, Juan José
Grau, Jaume
Hernández, Cristina
Guayta, Rafael
Pellisé, Maria
Macià, Francesc
Castellví-Bel, Sergi
Burón, Andrea
Esteban-Jurado, Clara
Hijona, Elizabeth
Abulí, Anna
Bujanda, Luis
Andreu, Montserrat
AuthorAffiliation 1 Department of Gastroenterology, Hospital del Mar, IMIM (Hospital del Mar Medical Research Institute), Pompeu Fabra University, Passeig Marítim 25–29, 08003, Barcelona, Catalonia, Spain
Sapporo Medical University, JAPAN
2 Department of Gastroenterology, Hospital Clínic, CIBERehd, IDIBAPS, University of Barcelona, Villarroel 170, 08036, Barcelona, Catalonia, Spain
7 Planning and Research Unit, Consell de Collegis Farmacèutics de Catalunya, Girona 64, 08009, Barcelona, Catalonia, Spain
4 Plataforma de Bioinformática, CIBERehd, Villarroel 170, 08036, Barcelona, Catalonia, Spain
6 Unitat d’Avaluació, Suport i Preventiva, Hospital Clínic, Roselló 138, 08036, Barcelona, Catalonia, Spain
3 Department of Gastroenterology, Hospital Donostia/Instituto Biodonostia, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Universidad del País Vasco (UPV/EHU), Doctor Begiristain Kalea, 20014, Donostia/Gipuzkoa, Spain
5 Department of Epidemiology and Evaluation, Hospital
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/27078840$$D View this record in MEDLINE/PubMed
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Sivilla, Judith
Balaguer, Francesc
Sala, Maria
Andreu, Montserrat
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Reig, Anna
Serradesanferm, Anna
Bessa, Xavier
Estrada, Maria
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Grau, Jaume
Castells, Xavier
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Augé, Josep M
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Copyright COPYRIGHT 2016 Public Library of Science
2016 Abulí et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
cc-by (c) Abulí, Anna et al., 2016 info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/3.0/es
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Competing Interests: The authors have declared that no competing interests exist.
All members of the PROCOLON group are listed in the Appendix.
Conceived and designed the experiments: AA AC JJL SCB MA. Performed the experiments: AA CH CEJ EH LB XB SCB. Analyzed the data: AA AC JJL CH SCB MA. Contributed reagents/materials/analysis tools: AA AC MA SCB LB XB CAU MP AB FM JG RG. Wrote the paper: AA MA JJL AC SCB. Selection of samples stored in the Biobank of Hospital del Mar and Hospital Donosti: AA EH.
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Snippet Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. To determine if these genetic variants are associated...
Background Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. Aim To determine if these genetic variants are...
Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. To determine if these genetic variants are associated...
BACKGROUNDCommon low-penetrance genetic variants have been consistently associated with colorectal cancer risk.AIMTo determine if these genetic variants are...
Background Common low-penetrance genetic variants have been consistently associated with colorec- tal cancer risk. Aim To determine if these genetic variants...
BACKGROUND:Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. AIM:To determine if these genetic variants are...
Background Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. Aim To determine if these genetic variants are...
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SubjectTerms Adenoma
Adenoma - genetics
Aged
Alleles
Analysis
Biology and Life Sciences
Cancer
Cancer screening
Case studies
Case-Control Studies
Chromosomes
Colon
Colonoscopy
Colonoscòpia
Colorectal cancer
Colorectal carcinoma
Colorectal Neoplasms - genetics
Càncer colorectal
Disease susceptibility
Epidemiology
Estudi de casos
Female
Gastroenterology
Gene Frequency
Genetic aspects
Genetic diversity
Genetic Predisposition to Disease - genetics
Genetic variance
Genetic variation
Genome-Wide Association Study
Genomes
Genotype
Genètica humana
Health risks
Hospitals
Human genetics
Humans
Lesions
Logistic Models
Male
Medical research
Medicine and Health Sciences
Middle Aged
Mortality
Multivariate Analysis
Mutació (Biologia)
Mutation (Biology)
Patients
Physiological aspects
Polymorphism, Single Nucleotide
Research and Analysis Methods
Risk
Risk Assessment - methods
Risk Assessment - statistics & numerical data
Risk Factors
Screening
Statistical analysis
Studies
Tumors
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Title Genetic Variants Associated with Colorectal Adenoma Susceptibility
URI https://www.ncbi.nlm.nih.gov/pubmed/27078840
https://www.proquest.com/docview/1781154732
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https://recercat.cat/handle/2072/268348
https://pubmed.ncbi.nlm.nih.gov/PMC4831735
https://doaj.org/article/31f74295138046c88a01528f00aae889
http://dx.doi.org/10.1371/journal.pone.0153084
Volume 11
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