Genetic Variants Associated with Colorectal Adenoma Susceptibility
Fecha
2016-04-14Autor
Abulí, Anna
Castells, Antoni
Lozano, Juan José
Bessa, Xavier
Hernández, Cristina
Álvarez-Urturi, Cristina
Pellisé, María
Esteban-Jurado, Clara
Hijona Muruamendiaraz, Elizabeth
Burón, Andrea
Macià, Francesc
Grau, Jaume
Guayta, Rafael
Castellví-Bel, Sergi
Andreu, Montserrat
PROCOLON research group
Metadatos
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PLOS ONE 11(4) : (2016) // Article ID e0153084
Resumen
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.
Colecciones
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