TY - JOUR T1 - Discovery of predictors of sudden cardiac arrest in diabetes: rationale and outline of the RESCUED (REcognition of Sudden Cardiac arrest vUlnErability in Diabetes) project JF - Open Heart JO - Open Heart DO - 10.1136/openhrt-2020-001554 VL - 8 IS - 1 SP - e001554 AU - Laura H van Dongen AU - Peter P Harms AU - Mark Hoogendoorn AU - Dominic S Zimmerman AU - Elisabeth M Lodder AU - Leen M 't Hart AU - Ron Herings AU - Henk C P M van Weert AU - Giel Nijpels AU - Karin M A Swart AU - Amber A van der Heijden AU - Marieke T Blom AU - Petra J Elders AU - Hanno L Tan Y1 - 2021/02/01 UR - http://openheart.bmj.com/content/8/1/e001554.abstract N2 - Introduction Early recognition of individuals with increased risk of sudden cardiac arrest (SCA) remains challenging. SCA research so far has used data from cardiologist care, but missed most SCA victims, since they were only in general practitioner (GP) care prior to SCA. Studying individuals with type 2 diabetes (T2D) in GP care may help solve this problem, as they have increased risk for SCA, and rich clinical datasets, since they regularly visit their GP for check-up measurements. This information can be further enriched with extensive genetic and metabolic information.Aim To describe the study protocol of the REcognition of Sudden Cardiac arrest vUlnErability in Diabetes (RESCUED) project, which aims at identifying clinical, genetic and metabolic factors contributing to SCA risk in individuals with T2D, and to develop a prognostic model for the risk of SCA.Methods The RESCUED project combines data from dedicated SCA and T2D cohorts, and GP data, from the same region in the Netherlands. Clinical data, genetic data (common and rare variant analysis) and metabolic data (metabolomics) will be analysed (using classical analysis techniques and machine learning methods) and combined into a prognostic model for risk of SCA.Conclusion The RESCUED project is designed to increase our ability at early recognition of elevated SCA risk through an innovative strategy of focusing on GP data and a multidimensional methodology including clinical, genetic and metabolic analyses. ER -