The EU funded project ENDOTARGET aims to explore the relationship between gut microbiota, gut permeability, and systemic endotoxemia with a special focus on the three most abundant rheumatic diseases (RDs): osteoarthritis, rheumatoid arthritis and spondylarthritis.
The ENDOTARGET EU project, a 4-year EU initiative coordinated by Helsinki University Hospital, is approaching its halfway mark. Launched on January 1st, 2023, the consortium has worked diligently across nine interconnected work packages to investigate the link between gut microbiota, intestinal permeability, and systemic endotoxemia (SE). The aim is to uncover key factors that drive the transition from health to disease in rheumatic diseases (RDs) such as osteoarthritis (OA), rheumatoid arthritis (RA), and spondylarthritis (SpA).
After another six months of intensive work, the consortium reconvened virtually on October 7th to discuss the non-scientific work packages. This was followed by a hybrid meeting from October 11th to 12th in Stuttgart, Germany, hosted by project partner Steinbeis Europa Zentrum. During the gathering, consortium members engaged in in-depth discussions on the progress and challenges encountered across the various work packages. Steinbeis Europa Zentrum supports as project partner the communication and dissemination activities of the consortium, as well as the exploitation of the research results.
Another project milestone in the past six months was the successful submission of the 1st periodic report to the European Commission 18 months after the project started.
Some glimpses into the current work of the ENDOTARGET project:
Population Cohort Analysis: The ENDOTARGET consortium has been conducting comprehensive population cohort analyses to explore novel biomarkers and lifestyle factors influencing the health-to-disease transition in RA, SpA, and OA. The project includes 12 cohorts, with five being used for population analysis: FINRISK Cohort, Estonian Biobank Cohort (EstBB), Northern Finland Birth Cohort (NFBC), Helsinki Businessmen Cohort (HBS), and the Portuguese Cohort. Recently, >15.000 samples from ENDOTARGET- cohorts were analysed for several endotoxemia-surrogate biomarkers, such as biomarkers lipopolysaccharide binding protein (LBP) and soluble CD14. Moreover, the analysis of the intestinal permeability and inflammation biomarkers zonuline and intestinal type fatty acid binding protein (I-FABP) is currently ongoing.
Furthermore, ENDOTARGET has also established collaborations with the EU-HORIZON sister project GLYCANTRIGGER, testing the validity of glycans as biomarkers for Crohn’s disease.
Focused cohorts & in vitro studies: This task is dedicated to investigating the role of SE and gut permeability in the pathogenesis of RA, SpA, and related inflammatory diseases. A key accomplishment here has been the extensive collection and analysis of clinical samples across multiple cohorts, including RA, SpA, and healthy controls. This will help to uncover how SE influences immune responses and contributes to the progression of inflammatory diseases. So far, efforts have focused on the collection of patient biopsy samples and the implementation of the necessary technologies and protocols. This work also includes the set-up and testing of a novel gut-on-a-chip system for investigating the impact of lipopolysaccharides (LPS), outer membrane vesicles, and extracellular vesicles on gut barrier permeability and functionality.
Mechanistic and Proof-of-Concept Studies: We have made progress in understanding the role of LPS in OA and RA by in vitro studies. Key findings include the molecular dynamics of LPS in the intra-articular joints and characterisation of novel LPS-binding mechanisms. Further in vitro and in silico studies are ongoing. Next to this, we have established preliminary animal models to study the systemic and local effects of LPS on OA progression.
Intervention Studies: ENDOTARGET is developing different intervention studies that evaluate distinct mechanisms that may interfere with gut microbiota, barrier integrity, and endotoxemia. The fecal transplant study in SpA is ongoing and will finish recruitment by the end of this year. The TASTY study that analyses the effect of the Mediterranean diet enriched with fermented foods on rheumatoid arthritis is actively recruiting patients.
Data Integration and Analysis: This task aims to integrate the results of the different studies and to use them for disease prediction modelling. In close collaboration with WP1, efforts were centred on extracting, standardising, and harmonising the obtained data to ensure consistency before analysis. While progress continues, most of the remaining tasks will be implemented in the coming years.
Dissemination & Communication Highlights:
In October 2024, the ENDOTARGET EU Project partners Gonçalo Barreto (HUS) and Patrícia Costa Reis (iMM) were invited to the 2nd episode of the GlycanTrigger podcast to discuss the compelling topic: “How Gut Permeability Impacts Inflammatory and Autoimmune Diseases?”
On the 24th of October, the first ENDOTARGET webinar “Fecal Microbiota Transplantation as a treatment for microbiota dysbiosis associated conditions” took place with three interesting talks about FMT. Watch the recordings here: https://endotargetproject.eu/communication-material/
Mark your calendars for the 12th of December (18:00 - 19:30 CET) for the 2nd ENDOTARGET webinar. We will give you interesting insights into the relationship between food, gut microbiome, and rheumatic diseases. Further, we will inform you about our currently running TASTY study.
Register here: https://eveeno.com/319482806
Scientific Publications:
Pazos-Pérez, A.; et al. The Hepatokine RBP4 Links Metabolic Diseases to Articular Inflammation. Antioxidants. 2024. doi: 10.3390/antiox13010124.
Guillán-Fresco, M.; et al. Formononetin, a Beer Polyphenol with Catabolic Effects on Chondrocytes. Nutrients. 2023. doi: 10.3390/nu15132959
Charneca, S.; et al. Beyond Seasoning—The Role of Herbs and Spices in Rheumatic Diseases. Nutrients. 2023. doi: 10.3390/nu15122812
Franco-Trepat, E.; et al. β Boswellic Acid Blocks Articular Innate Immune Responses: An In Silico and In Vitro Approach to Traditional Medicine. Antioxidants. 2023. doi: 10.3390/antiox12020371
Project Coordinator Team
Helsinki University Hospital (HUS), Helsinki, Finland
Project Coordinator
Kari Eklund (Kari.eklund@hus.fi)
Deputy Project Coordinator
Gonçalo Barreto (Goncalo.barreto@helsinki.fi)
Project Manager
Ana Valkama (Ana.valkama@hus.fi)
Helsinki University Hospital (HUS), Helsinki, Finland
Kari Eklund (Kari.eklund@hus.fi)
http://www.endotargetproject.eu - Website
http://@ENDOTARGET EU Project - LinkedIn
http://@ENDOTARGET_EU - X
Criteria of this press release:
Journalists, Scientists and scholars
Medicine, Nutrition / healthcare / nursing
transregional, national
Research projects, Research results
English
You can combine search terms with and, or and/or not, e.g. Philo not logy.
You can use brackets to separate combinations from each other, e.g. (Philo not logy) or (Psycho and logy).
Coherent groups of words will be located as complete phrases if you put them into quotation marks, e.g. “Federal Republic of Germany”.
You can also use the advanced search without entering search terms. It will then follow the criteria you have selected (e.g. country or subject area).
If you have not selected any criteria in a given category, the entire category will be searched (e.g. all subject areas or all countries).