TY - JOUR
T1 - Multi-Omics Interdisciplinary Research Integration to Accelerate Dementia Biomarker Development (MIRIADE)
AU - Mavrina, Ekaterina
AU - Kimble, Leighann
AU - Waury, Katharina
AU - Gogishvili, Dea
AU - Gómez de San José, Nerea
AU - Das, Shreyasee
AU - Coppens, Salomé
AU - Fernandes Gomes, B. rbara
AU - Mravinacová, S. ra
AU - Wojdała, Anna Lidia
AU - Bolsewig, Katharina
AU - Bayoumy, Sherif
AU - Burtscher, Felicia
AU - the MIRIADE consortium
AU - Mohaupt, Pablo
AU - Willemse, Eline
AU - Teunissen, Charlotte
N1 - Funding Information:
SD is an employee of ADx NeuroSciences, Gent, Belgium. SC is an employee of National Measurement Laboratory at LGC, London, UK. CT has a collaboration contract with ADx Neurosciences, Quanterix, and Eli Lilly, performed contract research or received grants from AC-Immune, Axon Neurosciences, Bioconnect, Biogen, Brainstorm Therapeutics, Celgene, EIP Pharma, Eisai, PeopleBio, Quanterix, Roche, Toyama, and Vivoryon. She serves on editorial boards of Medidact Neurologie/Springer, Alzheimer Research and Therapy, Neurology: Neuroimmunology & Neuroinflammation, and is editor of a Neuromethods book Springer. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Funding Information:
This project has received funding from the European Union's Horizon 2020 research and innovation program under grant agreement number 860197.
Publisher Copyright:
Copyright © 2022 Mavrina, Kimble, Waury, Gogishvili, Gómez de San José, Das, Coppens, Fernandes Gomes, Mravinacová, Wojdała, Bolsewig, Bayoumy, Burtscher, Mohaupt, Willemse, Teunissen and the MIRIADE consortium.
PY - 2022/7/12
Y1 - 2022/7/12
N2 - Proteomics studies have shown differential expression of numerous proteins in dementias but have rarely led to novel biomarker tests for clinical use. The Marie Curie MIRIADE project is designed to experimentally evaluate development strategies to accelerate the validation and ultimate implementation of novel biomarkers in clinical practice, using proteomics-based biomarker development for main dementias as experimental case studies. We address several knowledge gaps that have been identified in the field. First, there is the technology-translation gap of different technologies for the discovery (e.g., mass spectrometry) and the large-scale validation (e.g., immunoassays) of biomarkers. In addition, there is a limited understanding of conformational states of biomarker proteins in different matrices, which affect the selection of reagents for assay development. In this review, we aim to understand the decisions taken in the initial steps of biomarker development, which is done via an interim narrative update of the work of each ESR subproject. The results describe the decision process to shortlist biomarkers from a proteomics to develop immunoassays or mass spectrometry assays for Alzheimer's disease, Lewy body dementia, and frontotemporal dementia. In addition, we explain the approach to prepare the market implementation of novel biomarkers and assays. Moreover, we describe the development of computational protein state and interaction prediction models to support biomarker development, such as the prediction of epitopes. Lastly, we reflect upon activities involved in the biomarker development process to deduce a best-practice roadmap for biomarker development.
AB - Proteomics studies have shown differential expression of numerous proteins in dementias but have rarely led to novel biomarker tests for clinical use. The Marie Curie MIRIADE project is designed to experimentally evaluate development strategies to accelerate the validation and ultimate implementation of novel biomarkers in clinical practice, using proteomics-based biomarker development for main dementias as experimental case studies. We address several knowledge gaps that have been identified in the field. First, there is the technology-translation gap of different technologies for the discovery (e.g., mass spectrometry) and the large-scale validation (e.g., immunoassays) of biomarkers. In addition, there is a limited understanding of conformational states of biomarker proteins in different matrices, which affect the selection of reagents for assay development. In this review, we aim to understand the decisions taken in the initial steps of biomarker development, which is done via an interim narrative update of the work of each ESR subproject. The results describe the decision process to shortlist biomarkers from a proteomics to develop immunoassays or mass spectrometry assays for Alzheimer's disease, Lewy body dementia, and frontotemporal dementia. In addition, we explain the approach to prepare the market implementation of novel biomarkers and assays. Moreover, we describe the development of computational protein state and interaction prediction models to support biomarker development, such as the prediction of epitopes. Lastly, we reflect upon activities involved in the biomarker development process to deduce a best-practice roadmap for biomarker development.
KW - assay development
KW - biomarkers
KW - cerebrospinal fluid
KW - dementia
KW - immunoassays
KW - implementation
KW - mass spectrometry
UR - http://www.scopus.com/inward/record.url?scp=85135066201&partnerID=8YFLogxK
U2 - 10.3389/fneur.2022.890638
DO - 10.3389/fneur.2022.890638
M3 - Article
C2 - 35903119
SN - 1664-2295
VL - 13
JO - Frontiers in Neurology
JF - Frontiers in Neurology
M1 - 890638
ER -