JSM 2004 - Toronto

Abstract #301698

This is the preliminary program for the 2004 Joint Statistical Meetings in Toronto, Canada. Currently included in this program is the "technical" program, schedule of invited, topic contributed, regular contributed and poster sessions; Continuing Education courses (August 7-10, 2004); and Committee and Business Meetings. This on-line program will be updated frequently to reflect the most current revisions.

To View the Program:
You may choose to view all activities of the program or just parts of it at any one time. All activities are arranged by date and time.

The views expressed here are those of the individual authors
and not necessarily those of the ASA or its board, officers, or staff.


Back to main JSM 2004 Program page



Activity Number: 72
Type: Topic Contributed
Date/Time: Monday, August 9, 2004 : 8:30 AM to 10:20 AM
Sponsor: Section on Statistics in Epidemiology
Abstract - #301698
Title: Modeling Measurement Error in a Biomarker on the Pathway from Smoking to Lung Cancer
Author(s): Sally W. Thurston*+
Companies: University of Rochester
Address: Dept. of Biostatistics and Computational Biology, Rochester, NY, 14642,
Keywords: Bayesian ; biomarker ; DNA adducts ; lung cancer ; measurement error ; smoking
Abstract:

Molecular biologists have identified specific cellular changes, called biomarkers, which enable them to better characterize the pathway from chemical exposure to initiation of some cancers. In lung cancer, one such biomarker is DNA adducts in lung tissue. Carcinogens derived from cigarette smoke can bind to DNA to form such adducts, and this process is believed to initiate smoking-induced lung cancer. The goal of this work is to incorporate knowledge of such underlying biological mechanisms into a useful statistical framework to improve cancer risk estimates. The model uses measurements of adducts in lung cells and in blood cells; the latter are needed because lung adducts cannot be measured in controls. Adduct measurements in each type of cell are known to vary within individuals. By introducing a latent variable for true lung DNA adducts, I allow for measurement error in both types of observed adduct measurements, but assume greater measurement error in blood adducts. Gibbs sampling is used to obtain the posterior distributions of model parameters. Predicted and observed case status agree for approximately 75% of the sample.


  • The address information is for the authors that have a + after their name.
  • Authors who are presenting talks have a * after their name.

Back to the full JSM 2004 program

JSM 2004 For information, contact jsm@amstat.org or phone (888) 231-3473. If you have questions about the Continuing Education program, please contact the Education Department.
Revised March 2004