Original Article
National database of familial cancer in Sweden
Article first published online: 6 DEC 1998
DOI: 10.1002/(SICI)1098-2272(1998)15:3<225::AID-GEPI2>3.0.CO;2-3
Copyright © 1998 Wiley-Liss, Inc.
Additional Information
How to Cite
Hemminki, K. and Vaittinen, P. (1998), National database of familial cancer in Sweden. Genet. Epidemiol., 15: 225–236. doi: 10.1002/(SICI)1098-2272(1998)15:3<225::AID-GEPI2>3.0.CO;2-3
Publication History
- Issue published online: 6 DEC 1998
- Article first published online: 6 DEC 1998
- Manuscript Accepted: 3 SEP 1997
- Manuscript Revised: 22 AUG 1997
- Manuscript Received: 15 APR 1997
- Abstract
- References
- Cited By
Keywords:
- familial cancer;
- susceptibility;
- genes;
- database;
- cancer families
Abstract
A family cancer database was constructed from the nationwide Swedish registries and includes ˜6 million persons and >30,000 cancers in offspring diagnosed at ages 15–51 years and their parents. A particular advantage of the database is that the contribution of both parental lineages on cancer risk can be examined. Cancer risk in the offspring was increased ˜1.1 times when the father had cancer, and no increase was noted when the mother had cancer. If both parents had cancer, the risk for sons was 1.4 and for daughters 1.3. The sites of increased cancer risk in the offspring were colorectum, breast, cervix, corpus uteri, ovary, testis, melanoma, eye, other endocrine glands, and multiple myeloma. The results among young and middle-age adults suggest that cancer in both parents increases the cancer risk in the offspring at many sites. The molecular genetic explanation may be that rare dominant single genes increase susceptibility at many sites, or that overlapping sets of genes control susceptibility at multiple sites. Genet. Epidemiol. 15:225–236, 1998. © 1998 Wiley-Liss, Inc.

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