Bayesian Variable Selection Methods for Matched Case-Control Studies

被引:5
作者
Asafu-Adjei, Josephine [1 ,2 ]
Tadesse, Mahlet G. [3 ]
Coull, Brent [4 ]
Balasubramanian, Raji [5 ]
Lev, Michael [6 ]
Schwamm, Lee [7 ]
Betensky, Rebecca [8 ]
机构
[1] Univ North Carolina Chapel Hill, Dept Biostat, 3104-E McGavran Greenberg Hall, Chapel Hill, NC 27515 USA
[2] Univ North Carolina Chapel Hill, Dept Nursing, 2005 Carrington Hall, Chapel Hill, NC 27515 USA
[3] Georgetown Univ, Dept Math & Stat, Washington, DC USA
[4] Harvard Sch Publ Hlth, Dept Biostat, Boston, MA USA
[5] Univ Massachusetts, Amherst, MA 01003 USA
[6] Massachusetts Gen Hosp, Dept Radiol, Boston, MA USA
[7] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[8] Harvard Univ, Cambridge, MA 02138 USA
基金
美国国家卫生研究院;
关键词
Bayesian analysis; conditional logistic regression; matched case-control studies; variable selection methods; GENE-EXPRESSION; MODEL SELECTION; INSULAR CORTEX; REGRESSION; DISEASE; LATERALIZATION; CLASSIFICATION; REGULARIZATION; CONVERGENCE; ASSOCIATION;
D O I
10.1515/ijb-2016-0043
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Matched case-control designs are currently used in many biomedical applications. To ensure high efficiency and statistical power in identifying features that best discriminate cases from controls, it is important to account for the use of matched designs. However, in the setting of high dimensional data, few variable selection methods account for matching. Bayesian approaches to variable selection have several advantages, including the fact that such approaches visit a wider range of model subsets. In this paper, we propose a variable selection method to account for case-control matching in a Bayesian context and apply it using simulation studies, a matched brain imaging study conducted at Massachusetts General Hospital, and a matched cardiovascular biomarker study conducted by the High Risk Plaque Initiative.
引用
收藏
页数:23
相关论文
共 50 条
[1]   Boosting for Correlated Binary Classification [J].
Adewale, Adeniyi J. ;
Dinu, Irina ;
Yasui, Yutaka .
JOURNAL OF COMPUTATIONAL AND GRAPHICAL STATISTICS, 2010, 19 (01) :140-153
[2]   Identification of a panel of sensitive and specific DNA methylation markers for squamous cell lung cancer [J].
Anglim, Paul P. ;
Galler, Janice S. ;
Koss, Michael N. ;
Hagen, Jeffrey A. ;
Turla, Sally ;
Campan, Mihaela ;
Weisenberger, Daniel J. ;
Laird, Peter W. ;
Siegmund, Kimberly D. ;
Laird-Offringa, Ite A. .
MOLECULAR CANCER, 2008, 7 (1)
[3]  
[Anonymous], 2010, TECHNICAL REPORT
[4]  
[Anonymous], STAT METHODS CANC RE, DOI DOI 10.1097/00002030-199912240-00009
[5]  
[Anonymous], 2006, Journal of the Royal Statistical Society, Series B
[6]   Variable importance in matched case-control studies in settings of high dimensional data [J].
Balasubramanian, Raji ;
Houseman, E. Andres ;
Coull, Brent A. ;
Lev, Michael H. ;
Schwamm, Lee H. ;
Betensky, Rebecca A. .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES C-APPLIED STATISTICS, 2014, 63 (04) :639-655
[7]   Optimal predictive model selection [J].
Barbieri, MM ;
Berger, JO .
ANNALS OF STATISTICS, 2004, 32 (03) :870-897
[8]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[9]   General methods for monitoring convergence of iterative simulations [J].
Brooks, SP ;
Gelman, A .
JOURNAL OF COMPUTATIONAL AND GRAPHICAL STATISTICS, 1998, 7 (04) :434-455
[10]  
CARROLL R.J., 1995, MEASUREMENT ERROR NO, V63