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Three decades of advancements in osteoarthritis research: insights from transcriptomic, proteomic, and metabolomic studies

Lookup NU author(s): Dr Sarah RiceORCiD

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This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND).


Abstract

© 2023 The AuthorsObjective: Osteoarthritis (OA) is a complex disease involving contributions from both local joint tissues and systemic sources. Patient characteristics, encompassing sociodemographic and clinical variables, are intricately linked with OA rendering its understanding challenging. Technological advancements have allowed for a comprehensive analysis of transcripts, proteomes and metabolomes in OA tissues/fluids through omic analyses. The objective of this review is to highlight the advancements achieved by omic studies in enhancing our understanding of OA pathogenesis over the last three decades. Design: We conducted an extensive literature search focusing on transcriptomics, proteomics and metabolomics within the context of OA. Specifically, we explore how these technologies have identified individual transcripts, proteins, and metabolites, as well as distinctive endotype signatures from various body tissues or fluids of OA patients, including insights at the single-cell level, to advance our understanding of this highly complex disease. Results: Omic studies reveal the description of numerous individual molecules and molecular patterns within OA-associated tissues and fluids. This includes the identification of specific cell (sub)types and associated pathways that contribute to disease mechanisms. However, there remains a necessity to further advance these technologies to delineate the spatial organization of cellular subtypes and molecular patterns within OA-afflicted tissues. Conclusions: Leveraging a multi-omics approach that integrates datasets from diverse molecular detection technologies, combined with patients’ clinical and sociodemographic features, and molecular and regulatory networks, holds promise for identifying unique patient endophenotypes. This holistic approach can illuminate the heterogeneity among OA patients and, in turn, facilitate the development of tailored therapeutic interventions.


Publication metadata

Author(s): Rai MF, Collins KH, Lang A, Maerz T, Geurts J, Ruiz-Romero C, June RK, Ramos Y, Rice SJ, Ali SA, Pastrello C, Jurisica I, Thomas Appleton C, Rockel JS, Kapoor M

Publication type: Article

Publication status: Published

Journal: Osteoarthritis and Cartilage

Year: 2023

Pages: epub ahead of print

Online publication date: 02/12/2023

Acceptance date: 29/11/2023

Date deposited: 19/02/2024

ISSN (print): 1063-4584

ISSN (electronic): 1522-9653

Publisher: Elsevier

URL: https://doi.org/10.1016/j.joca.2023.11.019

DOI: 10.1016/j.joca.2023.11.019

PubMed id: 38049029


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Funding

Funder referenceFunder name
Arthritis Research
Canada Foundation for Innovation (CFI #225404, #30865)
CIBER –Consorcio Centro de Investigación Biomédica en Red (CB06/01/0040)
European Union's Horizon 2020 research and innovation program (No874671)
Instituto de Salud Carlos II (ISCIII) (PI20/00793)
Instituto de Salud Carlos III
Ian Lawson van Toch Fund
Ministerio de Ciencia e Innovación and Unión Europea – European Regional Development Fund
Natural Sciences Research Council (NSERC #203475)
NIH/NIAMS Pathway to Independence Award (K99/R00 AR078949)
NSF (CMMI 1554708)
NIH (NIAMS R01AR073964)
Ontario Research Fund (RDI #34876, #RE010–020)
the Department of Defense (GRANT13696744)
Versus Arthritis (22615)
the Canada Research Chairs Program (CRC)
Xunta de Galicia (IN607D 2020/10)
the Dr. Ralph and Marian Falk Medical Research Trust (Catalyst Award)
the National Institutes of Health (R01AR080035, R21AR076487, R21AR080502, R21AR082016, UC2AR082186)
The Royal Society (RGS\R1\231319)

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