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ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock
BACKGROUND: The ShockOmics study (ClinicalTrials.gov identifier NCT02141607) is a multicenter prospective observational trial aimed at identifying new biomarkers of acute heart failure in circulatory shock, by means of a multiscale analysis of blood samples and hemodynamic data from subjects with ci...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4730667/ https://www.ncbi.nlm.nih.gov/pubmed/26822963 http://dx.doi.org/10.1186/s13049-016-0197-4 |
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author | Aletti, Federico Conti, Costanza Ferrario, Manuela Ribas, Vicent Bollen Pinto, Bernardo Herpain, Antoine Post, Emiel Romay Medina, Eduardo Barlassina, Cristina de Oliveira, Eliandre Pastorelli, Roberta Tedeschi, Gabriella Ristagno, Giuseppe Taccone, Fabio S. Schmid-Schönbein, Geert W. Ferrer, Ricard De Backer, Daniel Bendjelid, Karim Baselli, Giuseppe |
author_facet | Aletti, Federico Conti, Costanza Ferrario, Manuela Ribas, Vicent Bollen Pinto, Bernardo Herpain, Antoine Post, Emiel Romay Medina, Eduardo Barlassina, Cristina de Oliveira, Eliandre Pastorelli, Roberta Tedeschi, Gabriella Ristagno, Giuseppe Taccone, Fabio S. Schmid-Schönbein, Geert W. Ferrer, Ricard De Backer, Daniel Bendjelid, Karim Baselli, Giuseppe |
author_sort | Aletti, Federico |
collection | PubMed |
description | BACKGROUND: The ShockOmics study (ClinicalTrials.gov identifier NCT02141607) is a multicenter prospective observational trial aimed at identifying new biomarkers of acute heart failure in circulatory shock, by means of a multiscale analysis of blood samples and hemodynamic data from subjects with circulatory shock. METHODS AND DESIGN: Ninety septic shock and cardiogenic shock patients will be recruited in three intensive care units (ICU) (Hôpital Erasme, Université Libre de Bruxelles, Belgium; Hospital Universitari Mutua Terrassa, Spain; Hôpitaux Universitaires de Genève, Switzerland). Hemodynamic signals will be recorded every day for up to seven days from shock diagnosis (time T0). Clinical data and blood samples will be collected for analysis at: i) T1 < 16 h from T0; ii) T2 = 48 h after T0; iii) T3 = day 7 or before discharge or before discontinuation of therapy in case of fatal outcome; iv) T4 = day 100. The inclusion criteria are: shock, Sequential Organ Failure Assessment (SOFA) score > 5 and lactate levels ≥ 2 mmol/L. The exclusion criteria are: expected death within 24 h since ICU admission; > 4 units of red blood cells or >1 fresh frozen plasma transfused; active hematological malignancy; metastatic cancer; chronic immunodepression; pre-existing end stage renal disease requiring renal replacement therapy; recent cardiac surgery; Child-Pugh C cirrhosis; terminal illness. Enrollment will be preceded by the signature of the Informed Consent by the patient or his/her relatives and by the physician in charge. Three non-shock control groups will be included in the study: a) healthy blood donors (n = 5); b) septic patients (n = 10); c) acute myocardial infarction or patients with prolonged acute arrhythmia (n = 10). The hemodynamic data will be downloaded from the ICU monitors by means of dedicated software. The blood samples will be utilized for transcriptomics, proteomics and metabolomics (“-omics”) analyses. DISCUSSION: ShockOmics will provide new insights into the pathophysiological mechanisms underlying shock as well as new biomarkers for the timely diagnosis of cardiac dysfunction in shock and quantitative indices for assisting the therapeutic management of shock patients. |
format | Online Article Text |
id | pubmed-4730667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47306672016-01-29 ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock Aletti, Federico Conti, Costanza Ferrario, Manuela Ribas, Vicent Bollen Pinto, Bernardo Herpain, Antoine Post, Emiel Romay Medina, Eduardo Barlassina, Cristina de Oliveira, Eliandre Pastorelli, Roberta Tedeschi, Gabriella Ristagno, Giuseppe Taccone, Fabio S. Schmid-Schönbein, Geert W. Ferrer, Ricard De Backer, Daniel Bendjelid, Karim Baselli, Giuseppe Scand J Trauma Resusc Emerg Med Study Protocol BACKGROUND: The ShockOmics study (ClinicalTrials.gov identifier NCT02141607) is a multicenter prospective observational trial aimed at identifying new biomarkers of acute heart failure in circulatory shock, by means of a multiscale analysis of blood samples and hemodynamic data from subjects with circulatory shock. METHODS AND DESIGN: Ninety septic shock and cardiogenic shock patients will be recruited in three intensive care units (ICU) (Hôpital Erasme, Université Libre de Bruxelles, Belgium; Hospital Universitari Mutua Terrassa, Spain; Hôpitaux Universitaires de Genève, Switzerland). Hemodynamic signals will be recorded every day for up to seven days from shock diagnosis (time T0). Clinical data and blood samples will be collected for analysis at: i) T1 < 16 h from T0; ii) T2 = 48 h after T0; iii) T3 = day 7 or before discharge or before discontinuation of therapy in case of fatal outcome; iv) T4 = day 100. The inclusion criteria are: shock, Sequential Organ Failure Assessment (SOFA) score > 5 and lactate levels ≥ 2 mmol/L. The exclusion criteria are: expected death within 24 h since ICU admission; > 4 units of red blood cells or >1 fresh frozen plasma transfused; active hematological malignancy; metastatic cancer; chronic immunodepression; pre-existing end stage renal disease requiring renal replacement therapy; recent cardiac surgery; Child-Pugh C cirrhosis; terminal illness. Enrollment will be preceded by the signature of the Informed Consent by the patient or his/her relatives and by the physician in charge. Three non-shock control groups will be included in the study: a) healthy blood donors (n = 5); b) septic patients (n = 10); c) acute myocardial infarction or patients with prolonged acute arrhythmia (n = 10). The hemodynamic data will be downloaded from the ICU monitors by means of dedicated software. The blood samples will be utilized for transcriptomics, proteomics and metabolomics (“-omics”) analyses. DISCUSSION: ShockOmics will provide new insights into the pathophysiological mechanisms underlying shock as well as new biomarkers for the timely diagnosis of cardiac dysfunction in shock and quantitative indices for assisting the therapeutic management of shock patients. BioMed Central 2016-01-28 /pmc/articles/PMC4730667/ /pubmed/26822963 http://dx.doi.org/10.1186/s13049-016-0197-4 Text en © Aletti et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Aletti, Federico Conti, Costanza Ferrario, Manuela Ribas, Vicent Bollen Pinto, Bernardo Herpain, Antoine Post, Emiel Romay Medina, Eduardo Barlassina, Cristina de Oliveira, Eliandre Pastorelli, Roberta Tedeschi, Gabriella Ristagno, Giuseppe Taccone, Fabio S. Schmid-Schönbein, Geert W. Ferrer, Ricard De Backer, Daniel Bendjelid, Karim Baselli, Giuseppe ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock |
title | ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock |
title_full | ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock |
title_fullStr | ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock |
title_full_unstemmed | ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock |
title_short | ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock |
title_sort | shockomics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4730667/ https://www.ncbi.nlm.nih.gov/pubmed/26822963 http://dx.doi.org/10.1186/s13049-016-0197-4 |
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