Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study

Ann Oncol. 2011 Apr;22(4):903-909. doi: 10.1093/annonc/mdq465. Epub 2010 Oct 5.

Abstract

Background: Classical familial adenomatous polyposis (FAP) is characterized by the appearance of >100 colorectal adenomas.

Patients and methods: We screened the APC and MUTYH genes for mutations and evaluated the genotype-phenotype correlation in 136 Spanish classical FAP families.

Results: APC/MUTYH mutations were detected in 107 families. Sixty-four distinct APC point mutations were detected in 95 families of which all were truncating mutations. A significant proportion (39.6%) had not been previously reported. Mutations were spread over the entire coding region and great rearrangements were identified in six families. Another six families exhibited biallelic MUTYH mutations. No APC or MUTYH mutations were detected in 29 families. These APC/MUTYH-negative families showed clinical differences with the APC-positive families. A poor correlation between phenotype and mutation site was observed.

Conclusions: Our results highlight that a broad approach in the genetic study must be considered for classical FAP due to involvement of both APC and MUTYH and the heterogeneous spectrum of APC mutations observed in this Spanish population. The scarcely consistent genotype-phenotype correlation does not allow making specific recommendations regarding screening and management. Differences observed in APC/MUTYH-negative families may reflect a genetic basis other than mutations in APC and MUTYH genes for FAP predisposition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenomatous Polyposis Coli / epidemiology*
  • Adenomatous Polyposis Coli / genetics*
  • Adenomatous Polyposis Coli / pathology
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Child
  • Child, Preschool
  • Colorectal Neoplasms / epidemiology
  • Colorectal Neoplasms / genetics
  • DNA Glycosylases / genetics*
  • Genes, APC*
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Humans
  • Infant
  • Middle Aged
  • Point Mutation
  • Polyps / pathology
  • Spain

Substances

  • DNA Glycosylases
  • mutY adenine glycosylase