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Segregation analysis of squamous cell carcinoma of the head and neck: evidence for a major gene determining risk

Published online by Cambridge University Press:  01 November 1998

M. DE ANDRADE
Affiliation:
Department of Epidemiology, UT-MD Anderson Cancer Center, PO Box 189, 1515 Holcombe Blvd, Houston, Texas, USA
C. I. AMOS
Affiliation:
Department of Epidemiology, UT-MD Anderson Cancer Center, PO Box 189, 1515 Holcombe Blvd, Houston, Texas, USA
W. D. FOULKES
Affiliation:
Departments of Medicine and Human Genetics, McGill University, Montreal General Hospital, Montreal, Quebec, Canada, H3G 1A4
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Abstract

We and others have shown that a family history of squamous cell carcinoma of the head and neck (SCCHN) is a risk factor for this disease. We performed a segregation analysis on a dataset comprised of 1429 first-degree relatives of 242 unselected cases of SCCHN and 934 first-degree relatives of 156 spouse controls. Using the SAGE software, we demonstrated that a Mendelian model was favored and a model postulating a purely environmental cause of SCCHN was rejected. The model suggests that 18% of the population who smoke and drink are susceptible. The lifetime risk for non-smokers and non-drinkers who are heterozygotes for the susceptible allele is close to zero, but for those heterozygotes who smoke and drink the risk is 14% by age 70. These findings suggest that specific genetic factors account for a significant fraction of the risk of SCCHN associated with a family history of SCCHN.

Type
Research Article
Copyright
University College London 1998

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