Development of a blood-based gene expression algorithm for assessment of obstructive coronary artery disease in non-diabetic patients

被引:100
作者
Elashoff, Michael R. [1 ]
Wingrove, James A. [1 ]
Beineke, Philip [1 ]
Daniels, Susan E. [1 ]
Tingley, Whittemore G. [2 ]
Rosenberg, Steven [1 ]
Voros, Szilard [3 ]
Kraus, William E. [4 ,5 ]
Ginsburg, Geoffrey S. [4 ,5 ]
Schwartz, Robert S. [6 ]
Ellis, Stephen G. [7 ]
Tahirkheli, Naheem [8 ]
Waksman, Ron [9 ]
McPherson, John [10 ]
Lansky, Alexandra J. [11 ]
Topol, Eric J. [12 ]
机构
[1] CardioDx Inc, Palo Alto, CA 94602 USA
[2] Univ Calif San Francisco, Div Cardiol, San Francisco, CA 94143 USA
[3] Piedmont Heart Inst, Fuqua Heart Ctr, Atlanta, GA 30309 USA
[4] Duke Univ, Sch Med, Dept Cardiol, Durham, NC 27710 USA
[5] Duke Univ, Sch Med, Ctr Genom Med, Durham, NC 27710 USA
[6] Minneapolis Heart Inst & Fdn, Minneapolis, MN 55407 USA
[7] Cleveland Clin Fdn, Dept Cardiovasc Med, Cleveland, OH 44195 USA
[8] Oklahoma Cardiovasc Res Grp, Oklahoma City, OK 73109 USA
[9] Medstar Res Inst, Cardiovasc Res Inst, Washington, DC 20010 USA
[10] Vanderbilt Heart & Vasc Inst, Dept Med, Nashville, TN 37232 USA
[11] Yale Univ, Med Ctr, Dept Med, New Haven, CT 06520 USA
[12] Scripps Translat Sci Inst, La Jolla, CA 92037 USA
关键词
CARDIOVASCULAR RISK; ATHEROSCLEROSIS; RECEPTOR; VALIDATION; DEPLETION; SELECTION; WOMEN;
D O I
10.1186/1755-8794-4-26
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Background: Alterations in gene expression in peripheral blood cells have been shown to be sensitive to the presence and extent of coronary artery disease (CAD). A non-invasive blood test that could reliably assess obstructive CAD likelihood would have diagnostic utility. Results: Microarray analysis of RNA samples from a 195 patient Duke CATHGEN registry case: control cohort yielded 2,438 genes with significant CAD association (p < 0.05), and identified the clinical/demographic factors with the largest effects on gene expression as age, sex, and diabetic status. RT-PCR analysis of 88 CAD classifier genes confirmed that diabetic status was the largest clinical factor affecting CAD associated gene expression changes. A second microarray cohort analysis limited to non-diabetics from the multi-center PREDICT study (198 patients; 99 case: control pairs matched for age and sex) evaluated gene expression, clinical, and cell population predictors of CAD and yielded 5,935 CAD genes (p < 0.05) with an intersection of 655 genes with the CATHGEN results. Biological pathway (gene ontology and literature) and statistical analyses (hierarchical clustering and logistic regression) were used in combination to select 113 genes for RT-PCR analysis including CAD classifiers, cell-type specific markers, and normalization genes. RT-PCR analysis of these 113 genes in a PREDICT cohort of 640 non-diabetic subject samples was used for algorithm development. Gene expression correlations identified clusters of CAD classifier genes which were reduced to meta-genes using LASSO. The final classifier for assessment of obstructive CAD was derived by Ridge Regression and contained sex-specific age functions and 6 meta-gene terms, comprising 23 genes. This algorithm showed a cross-validated estimated AUC = 0.77 (95% CI 0.73-0.81) in ROC analysis. Conclusions: We have developed a whole blood classifier based on gene expression, age and sex for the assessment of obstructive CAD in non-diabetic patients from a combination of microarray and RT-PCR data derived from studies of patients clinically indicated for invasive angiography.
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页数:14
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