TY - JOUR
T1 - Age-independent co-expression of antimicrobial gene clusters in the blood of septic patients
AU - Lindig, Sandro
AU - Quickert, Stefanie
AU - Vodovotz, Yoram
AU - Wanner, Guido A.
AU - Bauer, Michael
N1 - Funding Information:
Funding: This work was funded by the Federal Ministry of Education and Research (BMBF, 01EO1002 to MB and SL for the Center for Sepsis Control and Care , subprojects HDDP and TransSeptomics, respectively) and supported by the German Research Foundation (DFG) within the research unit FOR1738 (BA1601/8-1) and by grant P50-GM-53789 .
PY - 2013/6
Y1 - 2013/6
N2 - Recent research has unravelled the clinical potential of profiling the blood transcriptome to diagnose diseases. However, resulting molecular marker sets comprised features with varying robustness and performance, depending on the dimension of training data. Thus, we investigated patterns that are inherent in large-scale data and suitable for feature selection in application to blood samples from septic patients. By integrating >300 microarray samples in correlation and enrichment analysis, we found general response patterns including a vast majority of co-expressed genes. Differentially expressed genes significantly mapped to immune response-associated categories and revealed strongly correlating upregulated genes related to antimicrobial functions. Classifiers using >20 uncorrelated features from enriched functional categories performed with 85% correct classification on average (10-fold cross-validation), comparable with correlated features, whilst single genes achieved up to 83% correct classifications in identifying septic patients. Independent interplatform comparison, however, validated only a subset of these features, including the antimicrobial cluster (area under the receiver operating characteristic curve >0.8). Based on these results, we propose feature selection for classification incorporating correlation and enriched functional categories to obtain robust marker candidates. Results of this transcriptomic meta-analysis suggest age-independent diagnostic opportunities, although further observational and animal interventional experiments are required to confirm the relevance of antimicrobial genes in sepsis.
AB - Recent research has unravelled the clinical potential of profiling the blood transcriptome to diagnose diseases. However, resulting molecular marker sets comprised features with varying robustness and performance, depending on the dimension of training data. Thus, we investigated patterns that are inherent in large-scale data and suitable for feature selection in application to blood samples from septic patients. By integrating >300 microarray samples in correlation and enrichment analysis, we found general response patterns including a vast majority of co-expressed genes. Differentially expressed genes significantly mapped to immune response-associated categories and revealed strongly correlating upregulated genes related to antimicrobial functions. Classifiers using >20 uncorrelated features from enriched functional categories performed with 85% correct classification on average (10-fold cross-validation), comparable with correlated features, whilst single genes achieved up to 83% correct classifications in identifying septic patients. Independent interplatform comparison, however, validated only a subset of these features, including the antimicrobial cluster (area under the receiver operating characteristic curve >0.8). Based on these results, we propose feature selection for classification incorporating correlation and enriched functional categories to obtain robust marker candidates. Results of this transcriptomic meta-analysis suggest age-independent diagnostic opportunities, although further observational and animal interventional experiments are required to confirm the relevance of antimicrobial genes in sepsis.
KW - Blood
KW - Sepsis
KW - Transcriptomic markers
UR - http://www.scopus.com/inward/record.url?scp=84879086212&partnerID=8YFLogxK
U2 - 10.1016/j.ijantimicag.2013.04.012
DO - 10.1016/j.ijantimicag.2013.04.012
M3 - Article
C2 - 23684387
AN - SCOPUS:84879086212
SN - 0924-8579
VL - 42
SP - S2-S7
JO - International Journal of Antimicrobial Agents
JF - International Journal of Antimicrobial Agents
IS - SUPPL.1
ER -