Skip Navigation



Biostatistics Advance Access published online on June 1, 2006

Biostatistics, doi:10.1093/biostatistics/kxl006
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Supplementary Data
Right arrow All Versions of this Article:
8/2/252    most recent
kxl006v2
kxl006v1
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 Kang, M.
Right arrow Articles by Lagakos, S. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kang, M.
Right arrow Articles by Lagakos, S. W.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2006. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org
Received October 9, 2005
Revised May 18, 2006
Accepted May 31, 2006

Article

Statistical methods for panel data from a semi-Markov process, with application to HPV

Minhee Kang 1 * and Stephen W. Lagakos 1

1 Department of Biostatistics, Harvard University School of Public Health, 655 Huntington Avenue, Boston, Massachusetts 02115

* To whom correspondence should be addressed.
Minhee Kang, E-mail: mkang{at}hsph.harvard.edu


   Abstract

Continuous-time, multi-state processes can be used to represent a variety of biological processes in the public health sciences, yet the analysis of such processes is complex when they are observed only at a limited number of time points. Inference methods for such panel data have been developed for time-homogeneous Markov models, but there has been little research done for other classes of processes. We develop likelihood-based methods for panel data from a semi-Markov process, where transition intensities depend on the duration of time in the current state. The proposed methods account for possible misclassification of states. To illustrate the methods, we investigate a 3- and a 4-state models in detail and apply the results to model the natural history of oncogenic genital human papillomavirus (HPV) infections in women.

Keywords: Multi-state process; Misclassification; Natural history; Human papillomavirus.
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.