Abstract | BACKGROUND: MATERIALS AND METHODS: Early onset BCC cases (n=376) and controls with benign skin conditions (n=383) under age 40 were identified through Yale dermatopathology. Self-report data on family history of skin cancer ( melanoma and non- melanoma skin cancer), including age of onset in relatives, was available from a structured interview. Participants also provided saliva samples for sequencing of MC1R. RESULTS: A family history of skin cancer was associated with an increased risk of early-onset BCC (OR 2.49, 95% CI 1.80-3.45). In multivariate models, family history remained a strong risk factor for early-onset BCC after adjustment for pigment characteristics, UV exposure, and MC1R genotype (OR 2.41, 95% CI 1.74-3.35). CONCLUSIONS: Risk for BCC varied based upon the type and age of onset of skin cancer among affected relatives; individuals with a first-degree relative diagnosed with skin cancer prior to age 50 were at highest risk for BCC (OR 4.79, 95% CI 2.90-7.90). Even after taking into account potential confounding effects of MC1R genotype and various lifestyle factors that close relatives may share, family history of skin cancer remained strongly associated with early-onset BCC.
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Authors | Nicholas L Berlin, Brenda Cartmel, David J Leffell, Allen E Bale, Susan T Mayne, Leah M Ferrucci |
Journal | Cancer epidemiology
(Cancer Epidemiol)
Vol. 39
Issue 6
Pg. 1078-83
(Dec 2015)
ISSN: 1877-783X [Electronic] Netherlands |
PMID | 26381319
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2015. Published by Elsevier Ltd. |
Chemical References |
- Receptor, Melanocortin, Type 1
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Topics |
- Adult
- Aged
- Carcinoma, Basal Cell
(genetics)
- Case-Control Studies
- Female
- Genetic Predisposition to Disease
(genetics)
- Genotype
- Humans
- Male
- Middle Aged
- Receptor, Melanocortin, Type 1
(genetics)
- Risk Factors
- Skin Neoplasms
(genetics)
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