help button home button Genetics J Gen Phys
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
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 Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Aplenc, R.
Right arrow Articles by Propert, K. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Aplenc, R.
Right arrow Articles by Propert, K. J.
Genetics, Vol. 163, 1215-1219, March 2003, Copyright © 2003

Group Sequential Methods and Sample Size Savings in Biomarker-Disease Association Studies

R. Aplenca,b, H. Zhaob, T. R. Rebbecka, and K. J. Properta
a Department of Biostatistics and Epidemiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6021
b Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104

Corresponding author: R. Aplenc, 9th Fl., Blockley Hall, 423 Guardian Dr., Philadelphia, PA 19104-6021., raplenc{at}cceb.med.upenn.edu (E-mail)

Communicating editor: Z-B. ZENG

Molecular epidemiological association studies use valuable biosamples and incur costs. Statistical methods for early genotyping termination may conserve biosamples and costs. Group sequential methods (GSM) allow early termination of studies on the basis of interim comparisons. Simulation studies evaluated the application of GSM using data from a case-control study of GST genotypes and prostate cancer. Group sequential boundaries (GSB) were defined in the EAST-2000 software and were evaluated for study termination when early evidence suggested that the null hypothesis of no association between genotype and disease was unlikely to be rejected. Early termination of GSTM1 genotyping, which demonstrated no association with prostate cancer, occurred in >90% of the simulated studies. On average, 36.4% of biosamples were saved from unnecessary genotyping. In contrast, for GSTT1, which demonstrated a positive association, inappropriate termination occurred in only 6.6%. GSM may provide significant cost and sample savings in molecular epidemiology studies.





This article has been cited by other articles:


Home page
Hum Mol GenetHome page
M. E. Talkowski, G. Kirov, M. Bamne, L. Georgieva, G. Torres, H. Mansour, K. V. Chowdari, V. Milanova, J. Wood, L. McClain, et al.
A network of dopaminergic gene variations implicated as risk factors for schizophrenia
Hum. Mol. Genet., March 1, 2008; 17(5): 747 - 758.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 by the Genetics Society of America.