HarmonicSS — “HARMONIzation and integrative analysis of regional, national and international Cohorts on primary Sjögren’s Syndrome (pSS) towards improved stratification, treatment and health policy making”
- Project category EU Horizon 2020
- Lenght from 01.01.2017 to 30.06.2020
- Lab/Research Area Istituto di Management MeS
- Expected funding €9 998 750
- Costo complessivo €10 193 100
- Quota partner €200 000
- SSSA involvement Partner
- Website HarmonicSS website - EC H2020
- Sponsor European Commission
Da settembre 2016 Il Laboratorio MeS è partner, assieme ad altre 33 istituzioni internazionali, del progetto HarmonicSS “HARMONIzation and integrative analysis of regional, national and international Cohorts on primary Sjögren’s Syndrome (pSS) towards improved stratification, treatment and health policy making” che vede capofila il Dipartimento di fisiopatologia dell’Università di Atene, Grecia.
Il progetto, finanziato dalla Comunità Europea all’interno del programma Horizon2020 –Personalized medicine, ha come obiettivo quello di creare una piattaforma web che raccolga e armonizzi i dati di coorte di pazienti affetti da sindrome di Sjögren esistenti a livello internazionale. I dati raccolti verranno inizialmente analizzati da un gruppo multidisciplinare di medici, ricercatori in ambito di economia e management sanitario, informatici e ingegneri al fine di misurare e valutare la variabilità delle cure e trattamenti rivolti alle coorti di pazienti con sindrome di Sjögren e individuare percorsi 'virtuosi' e integrati per la loro presa in carico.
Responsabile Scientifico: Chiara Seghieri
Area di riferimento: Integrazione e gestione dei percorsi assistenziali complessi
Abstract (English only)
HarmonicSS vision is to create an International Network and Alliance of partners and cohorts, entrusted with the mission of addressing the unmet needs in primary Sjogren Syndrome; working together to create and maintain a platform with open standards and tools, designed to enable secure storage, governance, analytics, access control and controlled sharing of information at multiple levels along with methods to make results of analyses and outcomes comparable across centers and sustainable through Rheumatology associations. The overall idea of the HarmonicSS project is to bring together the largest well characterized regional, national and international longitudinal cohorts of patients with Primary Sjögren’s Syndrome (pSS) including those participating in clinical trials, and after taking into consideration the ethical, legal, privacy and IPR issues for sharing data from different countries, to semantically interlink and harmonize them into an integrative pSS cohort structure on the cloud. Upon this harmonized cohort, services for big data mining, governance and visual analytics will be integrated, to address the identified clinical and health policy pSS unmet needs. In addition, tools for specific diagnostic procedures (e.g. ultrasonography image segmentation), patient selection for clinical trials and training will be also provided. The users of the HarmonicSS platform are researchers (basic/translational), clinicians, health policy makers and pharma companies. pSS is relevant not only due to its clinical impact but also as one of the few “model” diseases to link autoimmunity, cancer development (lymphoproliferation) and the pathogenetic role of infection. Thus, the study of pSS can facilitate research in many areas of medicine; for this reason, the possibility for sustainability and expandability of the platform is enhanced. Moreover, pSS has a significant impact on the healthcare systems, similar to that of rheumatoid arthritis.