Pekka Martikainen , University of Helsinki
Kaarina Korhonen
Aline Jelenkovic, University of Helsinki
Aki Havulinna, National Institute for Health and Welfare
Samuli Ripatti, Institute for Molecular Medicine Finland
Katja Borodulin, National Institute for Health and Welfare
Veikko Salomaa, National Institute for Health and Welfare
Karri Silventoinen, University of Helsinki
Genetic vulnerability to coronary heart disease (CHD) is well established, but little is known whether these effects are mediated or modified by equally well-established social determinants of CHD. We used data derived from the 1992, 1997, 2002, 2007 and 2012 sweeps of the National FINRISK Study, including measures of social, behavioural and metabolic risk factors of CHD as well as genome wide scans (N=26203) with a follow-up for fatal and non-fatal CHD events (N=2063) until the end of 2015. Adjusted for age, sex, study year and region of residence, those who were in the highest quartile of genetic risk score (GRS) of CHD had an increased risk of CHD events (HR=2.55; 95% CI 2.24-2.90); strong associations were also observed for low education (HR=1.80; 95% CI 1.50-2.15). These effects were mainly independent of each other. Individuals with basic or vocational training and high genetic risk scores had particularly high CHD risk.
Presented in Session 142. Genes and Health - Using Polygenic Scores