TY - JOUR
T1 - Peripheral blood RNA biomarkers for cardiovascular disease from bench to bedside
T2 - a position paper from the EU-CardioRNA COST action CA17129
AU - Vanhaverbeke, Maarten
AU - Attard, Ritienne
AU - Bartekova, Monika
AU - Ben-Aicha, Soumaya
AU - Brandenburger, Timo
AU - De Gonzalo-Calvo, David
AU - Emanueli, Costanza
AU - Farrugia, Rosienne
AU - Grillari, Johannes
AU - Hackl, Matthias
AU - Kalocayova, Barbora
AU - Martelli, Fabio
AU - Scholz, Markus
AU - Wettinger, Stephanie Bezzina
AU - Devaux, Yvan
AU - EU-CardioRNA COST Action CA17129
N1 - DdGC has received financial support from Instituto de Salud Carlos III (Miguel Servet 2020: CP20/00041), co-funded by the European Social Fund (ESF) “Investing in your future”. CIBER Cardiovascular (CB16/11/00403 to DdG-C) is a project from Carlos III Health Institute. YD is funded by the EU Horizon 2020 project COVIRNA (Grant Agreement # 101016072), the National Research Fund (grants # C14/BM/8225223, C17/BM/11613033 and COVID-19/2020-1/14719577/miRCOVID), the Ministry of Higher Education and Research, and the Heart Foundation – Daniel Wagner of Luxembourg. CE is funded by the British Heart Foundation Programme Grant and Personal Chair Awards (RG/15/5/31446 and CH/15/1/31199), the EU Horizon projects MEDIRAD (NFRP Call) and COVIRNA (Grant Agreement # 101016072) and Research England (Global Challenges Research fund 2019/2021). MH is funded by the Eureka-Eurostars project THROMBOMIR through the FFG (Grant Agreement 871562). MB and BK are funded by the Scientific Grant Agency of the Ministry of Education, Science, Research and Sport of the Slovak Republic and the Slovak Academy of Sciences (grant VEGA no. 2/0104/20). FM is supported by the Italian Ministry of Health (“ricerca corrente” a 1 nd RF-2019-12368521, Telethon Foundation (#446 GGP19035A), AFM-Telethon (# 23054) and EU Horizon 2020 project COVIRNA (Grant #101016072).
© The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology.
PY - 2022/12/29
Y1 - 2022/12/29
N2 - Despite significant advances in the diagnosis and treatment of cardiovascular diseases, recent calls have emphasized the unmet need to improve precision-based approaches in cardiovascular disease. Although some studies provide preliminary evidence of the diagnostic and prognostic potential of circulating coding and non-coding RNAs, the complex RNA biology and lack of standardization have hampered the translation of these markers into clinical practice. In this position paper of the CardioRNA COST action CA17129, we provide recommendations to standardize the RNA development process in order to catalyse efforts to investigate novel RNAs for clinical use. We list the unmet clinical needs in cardiovascular disease, such as the identification of high-risk patients with ischaemic heart disease or heart failure who require more intensive therapies. The advantages and pitfalls of the different sample types, including RNAs from plasma, extracellular vesicles, and whole blood, are discussed in the sample matrix, together with their respective analytical methods. The effect of patient demographics and highly prevalent comorbidities, such as metabolic disorders, on the expression of the candidate RNA is presented and should be reported in biomarker studies. We discuss the statistical and regulatory aspects to translate a candidate RNA from a research use only assay to an in-vitro diagnostic test for clinical use. Optimal planning of this development track is required, with input from the researcher, statistician, industry, and regulatory partners.
AB - Despite significant advances in the diagnosis and treatment of cardiovascular diseases, recent calls have emphasized the unmet need to improve precision-based approaches in cardiovascular disease. Although some studies provide preliminary evidence of the diagnostic and prognostic potential of circulating coding and non-coding RNAs, the complex RNA biology and lack of standardization have hampered the translation of these markers into clinical practice. In this position paper of the CardioRNA COST action CA17129, we provide recommendations to standardize the RNA development process in order to catalyse efforts to investigate novel RNAs for clinical use. We list the unmet clinical needs in cardiovascular disease, such as the identification of high-risk patients with ischaemic heart disease or heart failure who require more intensive therapies. The advantages and pitfalls of the different sample types, including RNAs from plasma, extracellular vesicles, and whole blood, are discussed in the sample matrix, together with their respective analytical methods. The effect of patient demographics and highly prevalent comorbidities, such as metabolic disorders, on the expression of the candidate RNA is presented and should be reported in biomarker studies. We discuss the statistical and regulatory aspects to translate a candidate RNA from a research use only assay to an in-vitro diagnostic test for clinical use. Optimal planning of this development track is required, with input from the researcher, statistician, industry, and regulatory partners.
KW - Biomarkers
KW - Cardiovascular disease
KW - Gene expression
KW - Genomics
KW - Methodology standardization
KW - RNAs
KW - Transcriptomics
KW - Translational cardiovascular research
UR - http://www.scopus.com/inward/record.url?scp=85124872744&partnerID=8YFLogxK
UR - https://www.ncbi.nlm.nih.gov/pubmed/34648023
U2 - 10.1093/cvr/cvab327
DO - 10.1093/cvr/cvab327
M3 - Review article
C2 - 34648023
SN - 0008-6363
VL - 118
SP - 3183
EP - 3197
JO - Cardiovascular Research
JF - Cardiovascular Research
IS - 16
ER -