Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by GOLDSTEIN, A. M.
Right arrow Articles by HODGE, S. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by GOLDSTEIN, A. M.
Right arrow Articles by HODGE, S. E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

American Journal of Epidemiology Vol. 132, No. 6: 1171-1175
Copyright © 1990 by The Johns Hopkins University School of Hygiene and Public Health


research-article

A PROBLEM IN IDENTIFYiNG RISK FACTORS FOR DISEASE USING SURROGATE EXPOSURE VARIABLES THAT ARE UNDER GENETIC CONTROL

ALISA M. GOLDSTEIN1,, RONI T. FALK2 and SUSAN E. HODGE3

1Family Studies Section, Environmental Epidemiology Branch, National Cancer Institute, National Institutes of Health Bethesda, MD
2Population Studies Section, Environmental Epidemiology Branch, National Cancer Institute, National Institutes of Health Bethesda, MD
3Department of Psychiatry and Bioatatistics, New York State Psychiatric Institute, Columbia University New York, NY

Reprint requests to Dr. Alisa M. Goldstein, Family Studies Section/EEB, National Cancer Institute, National Institutes of Health, Executive Plaza North, Room 439, Bethesda, MD 20892

The use of a surrogate exposure variable to represent a complex of genetic and/or nongenetic factors is commonplace in epidemiologic studies. The authors present an hypothetical example in which a surrogate exposure results from underlying unknown genetic and nongenetic factors, yet only the genetic component predisposes to disease. The results demonstrate how risk may be incorrectly attributed to the nongenetic component of exposure and suggest a possible explanation for the identification of a risk factor in one case-control study in one population, but not in another study of the same disease conducted in a different population.

case-control studies; genetics; risk factors


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.