Abstract |
Colorectal cancer (CRC) risk is well defined for families of patients with classical familial adenomatous polyposis (FAP). However, the risk for those with an attenuated form of FAP is less well characterised. In this study, we estimated CRC risks for carriers of a novel germline mutation in the APC gene that causes attenuated FAP (AFAP). We performed genetic testing on 53 individuals from seven AFAP families harbouring an identical APC:c.288T>A mutation. Using a modified segregation analysis, we estimated relative and absolute CRC risks for mutation carriers. Twenty-three individuals harboured the disease causing mutation. CRC occurred in 28 individuals (mean 61.7 years, range 32-80 years). The estimated CRC relative risks for mutation carriers aged 60-69 and ≥70 years were 19 (95% CI: 1.77-204.08) and 45 (95% CI: 11.32-180.10), respectively, while the absolute CRC lifetime risk for men was 94% (95% CI: 67.5-99.9%), and for women, 84% (95% CI: 50.9-99.0%). This study shows that AFAP can manifest as autosomal dominant late-onset CRC. These findings highlight a subgroup of inherited CRCs that require new criteria for identification and surveillance.
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Authors | Abdulla Ibrahim, Daniel R Barnes, Jacqueline Dunlop, Daniel Barrowdale, Antonis C Antoniou, Jonathan N Berg |
Journal | European journal of human genetics : EJHG
(Eur J Hum Genet)
Vol. 22
Issue 11
Pg. 1330-3
(Nov 2014)
ISSN: 1476-5438 [Electronic] England |
PMID | 24549056
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- APC protein, human
- Adenomatous Polyposis Coli Protein
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Topics |
- Adenomatous Polyposis Coli
(complications, genetics)
- Adenomatous Polyposis Coli Protein
(genetics, metabolism)
- Adult
- Aged
- Colorectal Neoplasms
(complications, diagnosis, genetics)
- Exons
- Female
- Genetic Testing
- Germ-Line Mutation
- Humans
- Male
- Middle Aged
- Pedigree
- Risk Factors
- Young Adult
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