Charting a roadmap for heart failure biomarker studies

Standard

Charting a roadmap for heart failure biomarker studies. / Ahmad, Tariq; Fiuzat, Mona; Pencina, Michael J; Geller, Nancy L; Zannad, Faiez; Cleland, John G F; Snider, James V; Blankenberg, Stephan; Adams, Kirkwood F; Redberg, Rita F; Kim, Jae B; Mascette, Alice; Mentz, Robert J; O'Connor, Christopher M; Felker, G Michael; Januzzi, James L.

in: JACC-HEART FAIL, Jahrgang 2, Nr. 5, 10.2014, S. 477-488.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ReviewForschung

Harvard

Ahmad, T, Fiuzat, M, Pencina, MJ, Geller, NL, Zannad, F, Cleland, JGF, Snider, JV, Blankenberg, S, Adams, KF, Redberg, RF, Kim, JB, Mascette, A, Mentz, RJ, O'Connor, CM, Felker, GM & Januzzi, JL 2014, 'Charting a roadmap for heart failure biomarker studies', JACC-HEART FAIL, Jg. 2, Nr. 5, S. 477-488. https://doi.org/10.1016/j.jchf.2014.02.005

APA

Ahmad, T., Fiuzat, M., Pencina, M. J., Geller, N. L., Zannad, F., Cleland, J. G. F., Snider, J. V., Blankenberg, S., Adams, K. F., Redberg, R. F., Kim, J. B., Mascette, A., Mentz, R. J., O'Connor, C. M., Felker, G. M., & Januzzi, J. L. (2014). Charting a roadmap for heart failure biomarker studies. JACC-HEART FAIL, 2(5), 477-488. https://doi.org/10.1016/j.jchf.2014.02.005

Vancouver

Ahmad T, Fiuzat M, Pencina MJ, Geller NL, Zannad F, Cleland JGF et al. Charting a roadmap for heart failure biomarker studies. JACC-HEART FAIL. 2014 Okt;2(5):477-488. https://doi.org/10.1016/j.jchf.2014.02.005

Bibtex

@article{055cdd898d9246c5adddfc5d5d3eb05d,
title = "Charting a roadmap for heart failure biomarker studies",
abstract = "Heart failure is a syndrome with a pathophysiological basis that can be traced to dysfunction in several interconnected molecular pathways. Identification of biomarkers of heart failure that allow measurement of the disease on a molecular level has resulted in enthusiasm for their use in prognostication and selection of appropriate therapies. However, despite considerable amounts of information available on numerous biomarkers, inconsistent research methodologies and lack of clinical correlations have made bench-to-bedside translations rare and left the literature with countless publications of varied quality. There is a need for a systematic and collaborative approach aimed at definitively studying the clinical benefits of novel biomarkers. In this review, on the basis of input from academia, industry, and governmental agencies, we propose a systematized approach based on adherence to specific quality measures for studies looking to augment current prediction model or use biomarkers to tailor therapeutics. We suggest that study quality, rather than results, should determine publication and propose a system for grading biomarker studies. We outline the need for collaboration between clinical investigators and statisticians to introduce more advanced statistical methodologies into the field of biomarkers that would allow for data from a large number of variables to be distilled into clinically actionable information. Lastly, we propose the creation of a heart failure biomarker consortium that would allow for a comprehensive list of biomarkers to be concomitantly analyzed in a pooled sample of randomized clinical trials and hypotheses to be generated for testing in biomarker-guided trials. Such a consortium could collaborate in sharing samples to identify biomarkers, undertake meta-analyses on completed trials, and spearhead clinical trials to test the clinical utility of new biomarkers. ",
keywords = "Biomarkers/blood, Cooperative Behavior, Heart Failure/blood, Humans, Prognosis, Research Design",
author = "Tariq Ahmad and Mona Fiuzat and Pencina, {Michael J} and Geller, {Nancy L} and Faiez Zannad and Cleland, {John G F} and Snider, {James V} and Stephan Blankenberg and Adams, {Kirkwood F} and Redberg, {Rita F} and Kim, {Jae B} and Alice Mascette and Mentz, {Robert J} and O'Connor, {Christopher M} and Felker, {G Michael} and Januzzi, {James L}",
note = "Copyright {\textcopyright} 2014 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.",
year = "2014",
month = oct,
doi = "10.1016/j.jchf.2014.02.005",
language = "English",
volume = "2",
pages = "477--488",
journal = "JACC-HEART FAIL",
issn = "2213-1779",
publisher = "Elsevier BV",
number = "5",

}

RIS

TY - JOUR

T1 - Charting a roadmap for heart failure biomarker studies

AU - Ahmad, Tariq

AU - Fiuzat, Mona

AU - Pencina, Michael J

AU - Geller, Nancy L

AU - Zannad, Faiez

AU - Cleland, John G F

AU - Snider, James V

AU - Blankenberg, Stephan

AU - Adams, Kirkwood F

AU - Redberg, Rita F

AU - Kim, Jae B

AU - Mascette, Alice

AU - Mentz, Robert J

AU - O'Connor, Christopher M

AU - Felker, G Michael

AU - Januzzi, James L

N1 - Copyright © 2014 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

PY - 2014/10

Y1 - 2014/10

N2 - Heart failure is a syndrome with a pathophysiological basis that can be traced to dysfunction in several interconnected molecular pathways. Identification of biomarkers of heart failure that allow measurement of the disease on a molecular level has resulted in enthusiasm for their use in prognostication and selection of appropriate therapies. However, despite considerable amounts of information available on numerous biomarkers, inconsistent research methodologies and lack of clinical correlations have made bench-to-bedside translations rare and left the literature with countless publications of varied quality. There is a need for a systematic and collaborative approach aimed at definitively studying the clinical benefits of novel biomarkers. In this review, on the basis of input from academia, industry, and governmental agencies, we propose a systematized approach based on adherence to specific quality measures for studies looking to augment current prediction model or use biomarkers to tailor therapeutics. We suggest that study quality, rather than results, should determine publication and propose a system for grading biomarker studies. We outline the need for collaboration between clinical investigators and statisticians to introduce more advanced statistical methodologies into the field of biomarkers that would allow for data from a large number of variables to be distilled into clinically actionable information. Lastly, we propose the creation of a heart failure biomarker consortium that would allow for a comprehensive list of biomarkers to be concomitantly analyzed in a pooled sample of randomized clinical trials and hypotheses to be generated for testing in biomarker-guided trials. Such a consortium could collaborate in sharing samples to identify biomarkers, undertake meta-analyses on completed trials, and spearhead clinical trials to test the clinical utility of new biomarkers.

AB - Heart failure is a syndrome with a pathophysiological basis that can be traced to dysfunction in several interconnected molecular pathways. Identification of biomarkers of heart failure that allow measurement of the disease on a molecular level has resulted in enthusiasm for their use in prognostication and selection of appropriate therapies. However, despite considerable amounts of information available on numerous biomarkers, inconsistent research methodologies and lack of clinical correlations have made bench-to-bedside translations rare and left the literature with countless publications of varied quality. There is a need for a systematic and collaborative approach aimed at definitively studying the clinical benefits of novel biomarkers. In this review, on the basis of input from academia, industry, and governmental agencies, we propose a systematized approach based on adherence to specific quality measures for studies looking to augment current prediction model or use biomarkers to tailor therapeutics. We suggest that study quality, rather than results, should determine publication and propose a system for grading biomarker studies. We outline the need for collaboration between clinical investigators and statisticians to introduce more advanced statistical methodologies into the field of biomarkers that would allow for data from a large number of variables to be distilled into clinically actionable information. Lastly, we propose the creation of a heart failure biomarker consortium that would allow for a comprehensive list of biomarkers to be concomitantly analyzed in a pooled sample of randomized clinical trials and hypotheses to be generated for testing in biomarker-guided trials. Such a consortium could collaborate in sharing samples to identify biomarkers, undertake meta-analyses on completed trials, and spearhead clinical trials to test the clinical utility of new biomarkers.

KW - Biomarkers/blood

KW - Cooperative Behavior

KW - Heart Failure/blood

KW - Humans

KW - Prognosis

KW - Research Design

U2 - 10.1016/j.jchf.2014.02.005

DO - 10.1016/j.jchf.2014.02.005

M3 - SCORING: Review article

C2 - 24929535

VL - 2

SP - 477

EP - 488

JO - JACC-HEART FAIL

JF - JACC-HEART FAIL

SN - 2213-1779

IS - 5

ER -