Evidence map›Paper›PMID 21098433›Full record

ArticleBioinformatics (Oxford, England)2011

Prognostic transcriptional association networks: a new supervised approach based on regression trees.

Isabel Nepomuceno-Chamorro, Francisco Azuaje, Yvan Devaux, Petr V Nazarov, Arnaud Muller, Jesús S Aguilar-Ruiz, Daniel R Wagner

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Isabel Nepomuceno-ChamorroDepartamento Lenguajes y Sistemas Informáticos, Universidad de Sevilla, Seville, Spain. inepomuceno@us.es
Francisco Azuaje
Yvan Devaux
Petr V Nazarov
Arnaud Muller
Jesús S Aguilar-Ruiz
Daniel R Wagner

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationThe 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 prediction-based 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.

resultsBefore 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. AVAILABILITY: The SATuRNo software is freely available at http://www.lsi.us.es/isanepo/toolsSaturno/.

Indexed as

AlgorithmsGene Regulatory NetworksGene ExpressionHumansLinear ModelsMyocardial InfarctionPrognosis

Identifiers

PMID21098433
PMCPMC3018815

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.