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Cancer Epidemiology Biomarkers & Prevention Vol. 14, 2449-2453, October 2005
© 2005 American Association for Cancer Research


Short Communication

Genetic Variation and Willingness to Participate in Epidemiologic Research: Data from Three Studies

Parveen Bhatti1, Alice J. Sigurdson1, Sophia S. Wang2, Jinbo Chen3, Nathaniel Rothman4, Patricia Hartge5, Andrew W. Bergen6 and Maria Teresa Landi6

1 Radiation Epidemiology Branch, 2 Hormonal and Reproductive Epidemiology Branch, 3 Biostatistics Branch, 4 Occupational and Environmental Epidemiology Branch, 5 Epidemiology and Biostatistics Program, and 6 Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Department of Health and Human Services, Bethesda, Maryland

Requests for reprints: Parveen Bhatti, Radiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Department of Health and Human Services, 6120 Executive Boulevard, EPS 7091, MSC 7238, Bethesda, MD 20892-7238. Phone: 301-496-7950; Fax: 301-402-0207. E-mail: bhattip{at}mail.nih.gov

The differences in common genetic polymorphism frequencies by willingness to participate in epidemiologic studies are unexplored, but the same threats to internal validity operate as for studies with nongenetic information. We analyzed single nucleotide polymorphism genotypes, haplotypes, and short tandem repeats among control groups from three studies with different recruitment designs that included early, late, and never questionnaire responders, one or more participation incentives, and blood or buccal DNA collection. Among 2,955 individuals, we compared 108 genotypes, 8 haplotypes, and 9 to 15 short tandem repeats by respondent type. Among our main comparisons, single nucleotide polymorphism genotype frequencies differed significantly (P < 0.05) between respondent groups in six instances, with 13 expected by chance alone. When comparing the odds of carrying a variant among the various response groups, 19 odds ratios were ≤0.70 or ≥1.40, levels that might be notably different. Among the various respondent group comparisons, haplotype and short tandem repeat frequencies were not significantly different by willingness to participate. We observed little evidence to suggest that genotype differences underlie response characteristics in molecular epidemiologic studies, but a greater variety of genes should be examined, including those related to behavioral traits potentially associated with willingness to participate. To the extent possible, investigators should evaluate their own genetic data for bias in response categories.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
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Molecular Cancer Research Cancer Prevention Research
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Copyright © 2005 by the American Association for Cancer Research.