Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer

Gastroenterology. 2014 May;146(5):1208-11.e1-5. doi: 10.1053/j.gastro.2014.01.022. Epub 2014 Jan 17.

Abstract

We studied 2332 individuals with monoallelic mutations in MUTYH among 9504 relatives of 264 colorectal cancer (CRC) cases with a MUTYH mutation. We estimated CRC risks through 70 years of age of 7.2% for male carriers of monoallelic mutations (95% confidence interval [CI], 4.6%-11.3%) and 5.6% for female carriers of monoallelic mutations (95% CI, 3.6%-8.8%), irrespective of family history. For monoallelic MUTYH mutation carriers with a first-degree relative with CRC diagnosed by 50 years of age who does not have the MUTYH mutation, risks of CRC were 12.5% for men (95% CI, 8.6%-17.7%) and 10% for women (95% CI, 6.7%-14.4%). Risks of CRC for carriers of monoallelic mutations in MUTYH with a first-degree relative with CRC are sufficiently high to warrant more intensive screening than for the general population.

Keywords: Base Excision Repair Gene; Colon Cancer; DNA Damage Response; Genetics.

Publication types

  • Multicenter Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Australia
  • Colorectal Neoplasms / genetics*
  • DNA Glycosylases / genetics*
  • Female
  • Genetic Predisposition to Disease
  • Heredity
  • Heterozygote
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • New Zealand
  • North America
  • Pedigree
  • Phenotype
  • Registries
  • Risk Assessment
  • Risk Factors

Substances

  • DNA Glycosylases
  • mutY adenine glycosylase