TY - JOUR
T1 - Prognostic transcriptional association networks
T2 - A new supervised approach based on regression trees
AU - Nepomuceno-Chamorro, Isabel
AU - Azuaje, Francisco
AU - Devaux, Yvan
AU - Nazarov, Petr V.
AU - Muller, Arnaud
AU - Aguilar-Ruiz, Jesús S.
AU - Wagner, Daniel R.
N1 - Funding Information:
Funding: In Luxembourg this research was in part supported by Fonds National de la Recherche (Luxembourg); Société pour la Recherche sur les Maladies Cardiovasculaires; Ministére de la Culture; de l’Enseignement Supérieur et de la Recherche. In Spain, it was in part supported by the Spanish Ministry of Science and Innovation under Grant TIN2007–68084–C02–00, and by the Plan Propio of the University of Seville.
PY - 2011/1
Y1 - 2011/1
N2 - Motivation: The application of information encoded in molecular networks for prognostic purposes is a crucial objective of systems biomedicine. This approach has not been widely investigated in the cardiovascular research area. Within this area, the prediction of clinical outcomes after suffering a heart attack would represent a significant step forward. We developed a new quantitative predictionbased method for this prognostic problem based on the discovery of clinically relevant transcriptional association networks. This method integrates regression trees and clinical class-specific networks, and can be applied to other clinical domains. Results: Before analyzing our cardiovascular disease dataset, we tested the usefulness of our approach on a benchmark dataset with control and disease patients. We also compared it to several algorithms to infer transcriptional association networks and classification models. Comparative results provided evidence of the prediction power of our approach. Next, we discovered new models for predicting good and bad outcomes after myocardial infarction. Using blood-derived gene expression data, our models reported areas under the receiver operating characteristic curve above 0.70. Our model could also outperform different techniques based on co-expressed gene modules. We also predicted processes that may represent novel therapeutic targets for heart disease, such as the synthesis of leucine and isoleucine.
AB - Motivation: The application of information encoded in molecular networks for prognostic purposes is a crucial objective of systems biomedicine. This approach has not been widely investigated in the cardiovascular research area. Within this area, the prediction of clinical outcomes after suffering a heart attack would represent a significant step forward. We developed a new quantitative predictionbased method for this prognostic problem based on the discovery of clinically relevant transcriptional association networks. This method integrates regression trees and clinical class-specific networks, and can be applied to other clinical domains. Results: Before analyzing our cardiovascular disease dataset, we tested the usefulness of our approach on a benchmark dataset with control and disease patients. We also compared it to several algorithms to infer transcriptional association networks and classification models. Comparative results provided evidence of the prediction power of our approach. Next, we discovered new models for predicting good and bad outcomes after myocardial infarction. Using blood-derived gene expression data, our models reported areas under the receiver operating characteristic curve above 0.70. Our model could also outperform different techniques based on co-expressed gene modules. We also predicted processes that may represent novel therapeutic targets for heart disease, such as the synthesis of leucine and isoleucine.
UR - http://www.scopus.com/inward/record.url?scp=78651455339&partnerID=8YFLogxK
U2 - 10.1093/bioinformatics/btq645
DO - 10.1093/bioinformatics/btq645
M3 - Article
C2 - 21098433
AN - SCOPUS:78651455339
SN - 1367-4803
VL - 27
SP - 252
EP - 258
JO - Bioinformatics
JF - Bioinformatics
IS - 2
ER -