Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer.
retrospective_cohort · Level III
Where this comes from
- Record sourced from PubMed, PMID 24444654.
- Also identified by DOI 10.1053/j.gastro.2014.01.022 and PMC identifier 3992182.
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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.
Medical subject headings
- Colorectal Neoplasms
- DNA Glycosylases
- Mutation