EAS Paediatric FH symposium

Welcome to the 8th EAS Paediatric Familial Hypercholesterolemia Symposium

Saturday, 3 May 2025, Glasgow, UK

This event will take place in Crowne Plaza Glasgow (Congress Rd, Glasgow G3 8QT, UK) 

Registration for FREE – Registration will open soon

Programme

Organised by:
Uma Ramaswami, Alison Cozens, Jeanine Roeters van Lennep, Urh Grošelj, Mafalda Bourbon, Kirsten Holven, Michal Vrablik, and Steve Humphries

09.00-09.05 Welcome – Uma Ramaswami & Alison Cozens & Jules Payne (HEART UK)
09.05-10.25 Clinical utility of knowing the underlying genetic cause of the FH phenotype in children
Chairs: Steve Humphries (UK) and Mafalda Bourbon (Portugal)
09.05-09.20 Development and implementation of a LDL-C Polygenic Risk Score (PRS) – Mafalda Bourbon (Portugal)
09.20-09.35 What do Health Care Professionals and Patients think of the usefulness of the LDL-C SNP Score: the UK experience – Lisa Gritzmacher (UK)
09.35-09.50 LPA and other new genes for the FH Phenotype – Marta Futema (UK)
09.50-10.05 Does knowing the genetic cause of FH help decide the best lipid-lowering treatment? – Gilles Lambert (France)
10.05-10.25 Panel Discussion
10.25-11.00 Coffee break
11.00-12.50 Do we need a new clinical FH diagnostic score for children? 
Chairs: Jeanine Roeters van Lennep (The Netherlands) and Uma Ramaswami (UK)
11.00-11.10 Process and consensus committee for EAS Guidelines – Jeanine Roeters van Lennep (Netherlands)
11.10-11.30 Update of the EAS Paediatric FH Guidelines: new recommendations for 2025 –  Albert Wiegman (Netherlands)
11.30-11.50 Italian algorithm for identifying children with FH – Ornella Guardamagna (Italy)
11.50-12.10 Validation of a child-modified DLCN score in FHSC children – TBC
12.10-12.30 How will the new Guidelines influence clinical practice and help in deciding when to initiate Lipid-lowering therapy – Uma Ramaswami (UK)
12.30 -12.50 Round table discussion with all Topic 3 speakers plus Patient Representative plus Alison Cozens plus Jules Payne (HEARTUK) and Magdalena Daccord (FH Europe Foundation)
12.50-13.50 Lunch break
13.50-15.00 Treating children with HoFH : novel agents and PCSK9i/ANGPTL3i
Chairs: Michal Vrablik (Czech Republic), Alison Cozens (UK) & Urh Grošelj (Slovenia)
13.50-14.05 Inhibiting PCSK9 and ANGPTL3– Derick Raal (South Africa)
14.05-14.20 Patient experience of monoclonal antibody treatment – TBC 
14.20-14.35 ANGPTL3 gene editing to treat HoFH – Amit Kehera (Verve, USA)
14.35-14.50 Use of Bempadoic Acid to treat chldren with HeFH Ioanna Gouni-Berthold (Germany)
14.50-15.00 Panel discussion
15.00-15.10 Voting for next year’s topics and Wrap up – Steve Humphries (UK)
15.10-16.30 Networking drinks